Na+/H+ Exchangers (NHEs) in Mammalian Sperm: Essential Contributors to Male Fertility

Preprint

Review

Na⁺/H⁺ Exchangers (NHEs) in Mammalian Sperm: Essential Contributors to Male Fertility

Altmetrics

Downloads

134

Views

Comments

A peer-reviewed article of this preprint also exists.

This version is not peer-reviewed

Submitted:

05 September 2023

Posted:

07 September 2023

You are already at the latest version

Alerts

Abstract

Na⁺/H⁺ exchangers (NHEs) are known to be important regulators of pH in multiple intracellular compartments of eukaryotic cells. Sperm function is especially dependent on changes in pH and thus it has been postulated that NHEs play important roles in regulating the intracellular pH of these cells. For example, in order to achieve fertilization, mature sperm must maintain a basal pH in the male reproductive tract and then alkalize in response to specific signals in the female reproductive tract during the capacitation process. Eight NHE isoforms are expressed in mammalian testis/sperm: NHE1, NHE3, NHE5, NHE8, NHA1, NHA2, NHE10, and NHE11. These NHE isoforms are expressed at varying times during spermatogenesis and localize to different subcellular structures in developing and mature sperm where they contribute to multiple aspects of sperm physiology and male fertility including proper sperm development/morphogenesis, motility, capacitation, and the acrosome reaction. Previous work has provided evidence for NHE3, NHE8, NHA1, NHA2, and NHE10 being critical for male fertility in mice and NHE10 has recently been shown to be essential for male fertility in humans. In this article we review what is known about each NHE isoform expressed in mammalian sperm and discuss the physiological significance of each NHE isoform with respect to male fertility.

Keywords:

Subject: Biology and Life Sciences - Cell and Developmental Biology

1. Introduction

The Na⁺/H⁺ exchangers (NHEs) are a branch of the cation/proton antiporter (CPA) superfamily of transporters that are found in the membranes of many cells. NHEs found on the plasma membrane of higher eukaryotic cells export intracellular protons (H⁺) using the energy stored in the inward directed sodium ion (Na⁺) electrochemical gradient established by the Na,K-ATPase [1]. By exporting protons, NHEs play an important role as regulators of intracellular pH in many cells [2,3,4,5,6] and thus affect a wide variety of cellular and physiological processes from brain function [7] to male fertility [8,9,10,11,12,13]. In addition to those found on the plasma membrane, other NHEs display a predominantly intracellular localization and are thought to play roles in regulating pH in intracellular compartments [14].

After ejaculation, sperm must undergo a maturation process in the female reproductive tract, known as capacitation, before they are able to bind to and fertilize an oocyte [15]. There are many signature molecular events that occur during capacitation, including: an increase in intracellular pH [2,16,17,18,19], increases in intracellular cAMP levels resulting in increased protein tyrosine phosphorylation [20,21,22], increased K⁺ permeability [23,24,25], hyperpolarization of the sperm plasma membrane [23,24,26,27], and an increase in intracellular Ca²⁺ [23,24,28,29]. Capacitation ultimately results in sperm hyperactivation and the ability to undergo the acrosome reaction which are events necessary for the sperm to be able to fertilize an oocyte.

Intracellular pH (pH_i) has long been known to be important for a wide range of physiological processes including sperm motility [16,30,31] as pH likely affects multiple proteins vital for sperm function such as the Ca²⁺ channel complex CatSper and the K⁺ channel SLO3 [23,24,28,32,33]. Studies have shown that the transition from the immotile to the motile state and/or from a less motile to a highly motile state of rat and bovine sperm is mediated through a rise in intracellular pH [2,16,17,18,19]. In fact, sperm pH_i positively correlates with both hyperactivated motility and successful in vitro fertilization (IVF) in normospermic human patients [34]. Moreover, it has been demonstrated that the outer dynein arms of human sperm contain a pH sensitive regulatory mechanism whereby a slight alkalization of the cytoplasm initiates and increases the enzymatic activity of dynein motor proteins and thus modulates flagellar motion [35].

There is ample evidence suggesting that NHE activity plays an important role in the regulation of intracellular pH and motility of sperm. For example, it has been suggested that the alkalization required for the initiation of motility in sea urchin sperm is mediated by NHE activity [31,36,37]. It has also been shown that amiloride, an inhibitor of NHEs, inhibits rat sperm motility suggesting the importance of Na⁺ influx and/or H⁺ efflux in mammalian sperm motility [2]. Furthermore, in human sperm, inhibition of NHE activity with a more specific NHE inhibitor, 5-N-ethyl-N-isopropyl amiloride (EIPA), or incubation in Na⁺ deficient media, results in the acidification of the cytoplasm in capacitated human sperm suggesting the importance of NHE activity in the regulation of sperm pH_i in humans [38,39]. Inhibition of NHE activity with another NHE-specific inhibitor, 5-(N,N- dimethyl)-amiloride (DMA), results in impaired CatSper and Slo3 activity in mouse sperm [33]. Finally, inactivating certain NHE genes in mice has been shown to negatively impact sperm motility and male fertility [8,9,10,11,40] and a recent clinical study found that a mutation in a NHE-encoding gene resulted in human male infertility [13].

Na⁺/H⁺ Exchangers are encoded by the SLC9 gene family of solute carriers. This gene family has been divided into three subfamilies, determined by sequence homology: the NHE subfamily (SLC9A1-SLC9A9 which encode NHE1-NHE9), the NHA subfamily (SLC9B1 and SLC9B2 which encode NHA1 and NHA2 (also known as NHEDC1 and NHEDC2)), and the mammalian sperm-NHE-like subfamily (SLC9C1 and SLC9C2 which encode NHE10 [also known as sNHE] and NHE11) [5,6,42] (Figure 1). The NHE subfamily contain a conserved NHE domain at the N-terminus of the protein and also contain a cytosolic C-terminus of varying length that serves different regulatory functions for the nine different isoforms [6] (Figure 2). The NHE subfamily can be further divided by subcellular localization: NHE1,2, 4 are known to localize to the plasma membrane, while NHE6, 7, and 9 are known to localize to membranes of intracellular organelles, while NHE3, NHE5, and NHE8 have been shown to localize to either the plasma membrane or intracellular organelles in certain tissues and conditions [5,6]. SLC9B1 and SLC9B2 cluster into their own subfamily because they show closer sequence homology to bacterial Na⁺/H⁺ antiporters (NHAs) than to mammalian NHEs [43] (Figure 2). Prokaryotic NHAs are electrogenic and transport Na⁺ out of the cell and H⁺ into the cell, driven by the H⁺ gradient established by H⁺-ATPases [1,44,45]. The SLC9C1 and SLC9C2 genes appear to exist only in metazoans [46] and cluster into the mammalian sperm-NHE-like subfamily because of their unique predicted protein structure containing a NHE domain at the N-terminus, followed by a voltage-sensing domain (VSD), and an intracellular cyclic nucleotide binding domain (CNBD) at the C-terminus [6,8,43] (Figure 2).

There are eight NHE protein isoforms known to be expressed in mammalian testis/sperm: NHE1, NHE3, NHE5, NHE8, NHA1, NHA2, NHE10, and NHE11 [8,9,10,40,42,48] (Figure 3 and Figure 4). In this review, we will be examining the NHE proteins that are known to be expressed in sperm as well as discussing their transport activity and the role that they play in sperm physiology. We will attempt to describe the significance of individual NHEs in male fertility and posit potential implications for human medicine and society.

2. SLC9C1 (NHE10/sNHE)

2.1. Molecular Genetics and Expression Patterns

The SLC9C1 gene is located on human Chromosome 3 and is comprised of 29 exons. Both the mouse and human NHE10 proteins are expected to contain 17 total transmembrane domains: the first thirteen transmembrane domains are predicted to encode an N-terminal NHE domain and the last four transmembrane domains are predicted to encode a voltage sensing domain (VSD). The C-terminus of NHE10 is predicted to encode an intracellular cyclic nucleotide binding domain (CNBD) [8]. The predicted structure of NHE10 suggests that the NHE transport activity of the protein may be regulated by cyclic nucleotides and/or sperm membrane potential (E_m). Additionally, recent work from our lab suggests that mouse, rat, and human SLC9C1 genes possess conserved, and unique, methylation-sensitive DNA regulatory elements that contribute towards maintaining its testis/sperm-specific expression [55].

Seminal work from the Garbers group [8] identified the first sperm-specific NHE and demonstrated its critical importance in mouse sperm motility and male fertility. The NHE10 (originally termed sNHE) cDNA was cloned from a mouse spermatid enriched cDNA library and the transcript was found to be exclusively expressed in testis in mouse and the NHE10 protein was found to localize to the principal piece of the mature mouse sperm flagellum [8].

2.2. Sperm Physiology and Fertility

NHE10 knockout (KO) mice exhibit normal testis and sperm morphologies but are completely infertile due to immotile sperm [8]. Interestingly, the cell permeable weak base NH₃ is able to rescue motility in about 20% of the NHE10 KO mouse sperm and partially rescue their ability to fertilize zona pellucida-free eggs during in vitro fertilization (IVF) experiments, suggesting that the immotility phenotype is caused, at least partially, by an acidic intracellular pH [8]. However, there is ample evidence that lack of cAMP also underlies the loss of sperm motility and infertility in the NHE10 KO mouse. cAMP analogs rescue motility of NHE10 KO mouse sperm and partially restore their ability to fertilize zona pellucida-free eggs in IVF experiments [8]. NHE10 knockout sperm do not undergo normal protein tyrosine phosphorylation under capacitating conditions, but the addition of cAMP analogs along with a phosphodiesterase inhibitor restore protein tyrosine phosphorylation levels back to wildtype levels [56]. NHE10 KO mouse sperm have reduced basal levels of cAMP and HCO₃^- sensitive cAMP synthesis is undetectable. Immunoblotting revealed that the full-length soluble adenylyl cyclase (sAC) protein is absent in NHE10 KO sperm, but levels of truncated sAC protein are similar in NHE10 KO and wildtype sperm. NHE10 appears to regulate the expression of full-length sAC at the protein level because the NHE10 KO and wildtype testes have comparable levels of full-length sAC mRNA. Cell culture experiments validated this hypothesis; co-transfection of NHE10 and sAC increased the expression of both the full length and truncated isoforms of sAC. It was also shown that expression of the carboxy terminus of NHE10 physically interacts with truncated sAC when coimmunoprecipitation studies were performed [56].

Optogenetics, using a transgenic mouse model that expresses a photoactivated adenylyl cyclase (bPAC) in the sperm, was used to further examine the functional relationship between sAC and NHE10 [57]. When bPAC mouse sperm are exposed to light, there is a rapid increase in intracellular cAMP synthesized by the transgenic photoactivated adenylyl cyclase. This bPAC mouse was bred into the NHE10 knockout mouse background. When bPAC/NHE10 KO mouse sperm are exposed to light, there is a rapid increase in cAMP, sperm motility is restored, and the sperm are able to fertilize zona pellucida-intact oocytes in vitro [57]. All of this is evidence that in mice, NHE10 is not necessary for sperm motility and fertilization following an increase in cAMP via sAC. However, NHE10 is necessary for proper sAC expression and subsequent cAMP synthesis in mouse sperm. It is still unclear exactly what physiological role NHE10 has upstream of the increase of cAMP signaling events, although a recent study suggests that NHE10 expression is necessary for mediating the hyperpolarization-mediated alkalization observed in the mouse sperm flagellum [58]. Of note, addition of cAMP analogs is only able to partially rescue in vitro fertility ~50% and cAMP synthesis via pBAC is only able to rescue in vitro fertility ~30% [57]. This partial rescue of fertility in the absence of NHE10 protein suggests that NHE10 plays other roles in sperm to support motility and fertility.

2.3. NHE10 Transport Activity

Initial attempts to characterize the transport activity of the NHE10 protein failed due to the inability to express the NHE10 protein in cultured cells. Eventually, the Garbers group was able to show very weak expression of mouse NHE10 in a human cell line (HEK 293F) that was co-transfected with a truncated isoform of mouse sAC [56]. In an effort to increase NHE10 expression, the same group created a chimeric NHE1-NHE10 protein in which the first transmembrane domain of the mouse NHE10 protein was replaced with the first three transmembrane domains of the mouse NHE1 protein. When transfected into HEK293F cells, this chimeric NHE1-NHE10 protein was expressed and localized to the plasma membrane. Expression of the chimeric NHE1-NHE10 protein in a NHE1-null fibroblast cell line conferred resistance to acid-loading selection and the chimeric transporter was shown to possess weak Na⁺/H⁺ exchange activity [56]. However, since it is not clear whether the minimal NHE activity reported for the NHE1-NHE10 chimeric protein [56] is present without the contribution of the NHE1 components, characterization of the native mammalian NHE10 proteins is critical to understand how the transport activity of NHE10 influences mammalian sperm physiology.

Unfortunately, no unmodified mammalian NHE10 has been shown to possess NHE activity to date. However, sea urchin express a single SLC9C protein (originally identified as NHE10) that has recently been shown to be a bona fide NHE whose activity is not affected by the NHE inhibitors amiloride, EIPA, cariporide, and phloretin [59]. Mammals possess two SLC9C proteins (NHE10 and NHE11 – see below) and the sea urchin protein is no more similar to mammalian NHE10 than mammalian NHE11 [42] making it impossible to determine whether it is a specific ortholog of either. Therefore, we will refer to the sea urchin isoform as the sea urchin SLC9C (suSLC9C) protein from here on.

Immunolocalization demonstrated that the suSLC9C protein resides in the plasma membrane of the entire sea urchin sperm flagellum as well as in part of the sperm head, potentially the acrosome [59]. The analyses of the suSLC9C protein also demonstrated that its NHE activity is enhanced in response to the egg peptide speract [59], confirming earlier work suggesting a voltage sensitive Na⁺/H⁺ exchange in sea urchin spermatazoa [60]. In addition, mass spectrometry revealed ~54,000 suSLC9C protein molecules in the flagellum of sea urchin Arbacia punctulata sperm, one of the most abundant proteins found in this study [61]. Such a concentration of suSLC9C protein molecules found in the flagellum would allow this sperm to rapidly fine tune pH_i in response to various cell signaling conditions.

The overall domain structure of suSLC9C protein is predicted to be similar to the structure predicted for the mouse NHE10 in that they both contain an N-terminal NHE domain, followed by a VSD, and then a C-terminal CNBD; each domain containing many conserved functional residues [59]. Electrophysiological characterization of suSLC9C protein expressed in cultured cells revealed that this NHE is an electroneutral Na⁺/H⁺ exchanger that can exchange in either direction, depending on the ion gradient [59]. The VSD of suSLC9C protein produces gating currents, suggesting that it is a functional voltage sensing domain. In addition, the NHE activity of the suSLC9C protein is voltage dependent with a V_1/2 < -70.9 mV and cyclic nucleotides modulated the V_1/2 of its activity: cAMP shifted the V_1/2 of exchange activity to -56.8 mV and cGMP shifted the V_1/2 of exchange activity to a lesser degree, to -67.8 mV [59]. These findings suggest that binding of cAMP to the CNBD of suSLC9C protein affects NHE activity by shifting the voltage dependence of activation. Although the suSLC9C protein has been confirmed to be a voltage and cyclic nucleotide-sensitive NHE, it was noted that specific amino acid residues in the suSLC9C protein VSD and CNBD, thought to be important for function, are not conserved in the mouse and human NHE10 orthologs [59]. Further studies are required to determine the activity of the mammalian proteins to determine whether mammalian NHE10 is an NHE that responds to changes in membrane potential and cyclic nucleotides to regulate sperm function like the suSLC9C protein does in sea urchin sperm.

A recent study found that NHE10 KO mouse sperm are unable to alkalize their principal piece in response to valinomycin-induced hyperpolarization in the same manner that WT mouse sperm can [58]. These experiments suggest that NHE10 is responsible for the hyperpolarization-induced alkalization in mouse sperm and that the NHE10 protein likely is able to regulate pH and is sensitive to membrane potential. However, it was found that human sperm do not alkalize in response to valinomycin-induced hyperpolarization [58]. It is therefore possible that the human NHE10 activity is not regulated by membrane potential, but further characterization of the function of the VSD of human NHE10 is necessary.

2.4. NHE10 and Human Fertility

Although few specifics about the transport activity of mammalian NHE10 are known, evidence points to human NHE10 having a critical role in male fertility. A recent clinical study found significantly less NHE10 protein in sperm from asthenozoospermic compared to normozoospermic men and that NHE10 expression was positively correlated with higher sperm motility parameters [12]. It was noted in this study that NHE10 is specifically localized to the principal piece of the human sperm flagellum [12], similar to what is seen in mouse sperm [8] however, human NHE10 is also reported to localize to the entire sperm flagellum [13]. Even more recent analysis of an infertile male presenting with asthenozoospermia found that this patient bares a homozygous mutation in the SLC9C1 gene [13]. This patient’s sperm displays severely impaired motility as well as characteristics indicating membrane and flagellar fragility. Transmission electron microscopy (TEM) analysis revealed that the sperm exhibits midpiece defects but no acrosomal or axonemal structural abnormalities were observed. The specific mutation caused aberrant splicing around exon 22 which is predicted to cause an in-frame deletion of 33 amino acids in the consensus cyclic nucleotide binding domain of NHE10. The mutant NHE10 protein is still produced and was reported to localized, like the wild-type NHE10, to the entire length of the sperm flagellum [13]. It should be noted that this patient also bares mutations in two other genes and therefore the possibility that the infertile phenotype is due to a combination of these mutations cannot be excluded. In addition, since the level of sAC was not assessed in these mutant sperm, it is not clear whether the infertility of this patient is due to defective transport from the mutant NHE10 protein, or if it affects sAC protein expression as is thought to occur in the mouse model completely lacking NHE10 (Wang et al., 2007). While these findings highlight the importance of NHE10 in human male fertility, more work is needed to dissect the exact functions and interactions of human NHE10. Due to its testis/sperm-specific expression and its recent evidence suggesting that it is essential to male fertility, NHE10 is an especially attractive target for a male contraceptive drug.

3. SLC9C2 (NHE11)

3.1. Molecular Genetics and Expression Patterns

The SLC9C2 gene is located on human Chromosome 1 and is comprised of 28 exons. NHE11 exhibits a testis/sperm-specific expression pattern in both rats and humans [42]. Like mammalian NHE10, the rat and human NHE11 proteins are also predicted to contain seventeen total transmembrane domains, the first thirteen transmembrane domains encompassing a NHE domain and the final four transmembrane constituting a VSD. NHE11 protein expression is first detectable in spermiogenic cells and appears to colocalize with the developing acrosomal granule in both rat and human testis sections. Interestingly, NHE11 localizes specifically to the sperm head, likely the plasma membrane overlaying the acrosome, in both rat and human mature sperm cells. This is significant as no other NHE is known to localize to this region of the sperm head in mature sperm cells [42].

It is currently unclear what the evolutionary relationship is between the SLC9C1 and SLC9C2 genes. Interestingly, in Mus musculus, SLC9C2 is annotated as a pseudogene (designated GM6185).

3.2. Sperm Physiology and Fertility

No study to date has characterized the function of the SLC9C2 gene in any mammal as a SLC9C2 knockout animal model is needed.

3.3. NHE11 Transport Activity

No study to date has characterized the biochemical activity of the NHE11 protein. However, many residues previously demonstrated to be essential for Na⁺/H⁺ exchange in suSLC9C protein and human NHE1 are also conserved to mammalian NHE11, suggesting that mammalian NHE11 is likely a functional NHE. Additionally, many residues of the VSD and CNBD shown to be important for responses to changes in membrane potential and cyclic nucleotide binding are conserved in mammalian NHE11 [42]. All of this data suggests that mammalian NHE11 is likely a NHE regulated by both membrane potential and cyclic nucleotides, like sea urchin SLC9C protein. However, experiments are necessary to confirm this.

3.4. NHE11 and Human Fertility

Publicly available RNA-sequencing (https://www.ncbi.nlm.nih.gov/gene/284525 and https://orit.research.bcm.edu/MRGDv2) and proteomics data (https://www.proteomicsdb.org/protein/64851/expression) suggests that NHE11 is expressed exclusively in the testis and sperm in humans. Additionally, human NHE11 localizes to the head of mature sperm cells, the only known NHE to do so [42]. Finally, two separate studies that performed mass spectrometry on mature human sperm detected NHE11 [62,63]. Further studies are necessary to determine the physiological significance of human NHE11.

4. SLC9B1 (NHA1/NHEDC1)

4.1. Molecular Genetics and Expression Patterns

The SLC9B1 gene is located on human Chromosome 4 and is comprised of 12 exons. The SLC9B1 gene appears to be the result of a tandem gene duplication event of an ancestral SLC9B2 gene, appearing first in early marsupial mammalian evolution [64]. Interestingly, after this gene duplication event, SLC9B1 gene expression evolved to exhibit testis/sperm-specific expression whereas SLC9B2 displays an ubiquitous expression pattern [10,65,66]. The human SLC9B1 gene is regulated by a single promoter with a CpG island that is methylation dependent [67]. This CpG island in the promoter region of SLC9B1 is hypomethylated in human testis and hypermethylated in human lung tissue; suggesting that methylation of this CpG associated promoter region inhibits NHA1 expression in somatic cells [67].

Several lines of evidence demonstrate that NHA1 is important for sperm motility and fertility, including its expression pattern. NHA1 is exclusively expressed in testis in developing sperm in mouse, rat, monkey, goat, bull, and human [10,67]. NHA1 is reported to specifically localize to the principal piece in mouse sperm [10], but has also been reported to localize across the entire flagellum [11]. Cloning of mouse NHA1 cDNA and recombinant expression in cell culture showed that the NHA1 protein localizes to the plasma membrane [11].

4.2. Sperm Physiology and Fertility

NHA1 DNA vaccines given to female mice generated antisera and vaginal fluid containing proteins that specifically recognize the principal piece of wildtype mouse sperm and triggered sperm agglutination, acting as a crude contraceptive [10,65,68]. The role of NHA1 in male fertility has subsequently been supported and expanded by results of studies utilizing knockout mouse models.

The first of two lines of NHA1 knockout mice were generated using the Cre-LoxP system: mice with a NHA1 “floxed” allele were crossed with transgenic mice expressing Cre recombinase under the control of the zona pellucida 3 (Zp3) gene promoter. The Zp3 promoter drives the expression of Cre in the oocyte resulting in a global knockout of NHA1 from a conditional allele. These conditional NHA1 knockout (NHA1 cKO) mouse testes and sperm exhibit normal morphologies and the sperm undergo the acrosome reaction at a rate comparable to wild-type sperm. However, these NHA1 cKO mice produced sperm with reduced motility resulting in subfertility [10]. The NHA1 cKO mouse testes and sperm also have diminished cAMP as well as reduced soluble adenylyl cyclase (sAC) protein levels, and the addition of cAMP analogs restores sperm motility to wildtype levels [10]. In transfected HEK293F cells, heterologous NHA1 expression increases endogenous sAC expression [10], reminiscent of what is seen in NHE10 transfected cell culture [56].

A second NHA1 knockout mouse model was generated and the knockout sperm display reduced motility and fertility [11], similar to the findings from the NHA1 cKO mice [10]. Interestingly, the sperm from this second NHA1 knockout were show to have a stiff midpiece [11]. Analysis of this second NHA1 knockout model demonstrated that NHA1 activity, not NHE10, is involved in the zona pellucida-induced alkalization observed in capacitated sperm [11]. Specifically, when NHA1 knockout mouse sperm were exposed to soluble zona pellucida proteins, both pH_i and Ca²⁺ increases were strongly attenuated compared to wildtype. Supporting the idea that NHA1 plays a role in pH_i and Ca²⁺ regulation in mouse sperm; previous studies demonstrated that wildtype mouse sperm treated with anti-NHA1 antisera displayed decreased motility as well as reduced pH_i and intracellular Ca²⁺ concentration [65]. However, db-cAMP (a cell permeant, non-hydrolyzable cAMP analog) did not rescue the pH_i and Ca²⁺ response to zona pellucida protein exposure in the second line of NHA1 knockout mice [11]. This suggests that NHA1 function is either directly or indirectly responsible for both pH_i and Ca²⁺ regulation in response to zona pellucida protein stimulation. Furthermore, wildtype and NHA1 knockout sperm beat frequency (with and without HCO₃^-) was similar [11]. These findings suggest that loss of NHA1 activity/expression underlies the abnormal phenotype of the NHA1-defficient sperm, rather than defective sAC functionality leading to impaired cAMP synthesis. Interesting, residual NHE activity (measured as intracellular alkalization) in response to zona pellucida proteins in NHA1 knockout sperm was observed and was suggested to be a contribution of either an unknown NHE, NHA2, or some combination of both [11]. This may explain why NHA1-deficient male mice are not completely infertile; there may be other NHE(s) that share functional redundancy with NHA1.

Two other vital ion transporters in mammalian sperm are the CatSper complex and the Slo3-Lrrc52 complexes. The CatSper complex forms a channel that is responsible for Ca²⁺ influx into the cell that is required for capacitation. CatSper is activated by an increase in pH_i, E_m, and progesterone in humans [29,69] but only by pH_i and E_m in mice [28]. The Slo3-Lrrc52 complex is responsible for the K⁺ influx observed in capacitation that in turn hyperpolarizes the E_m in mouse and human sperm, ultimately regulating pH_i and Ca²⁺ influx [23,24,70,71,72,73,74]. CatSper organization and density is similar in wildtype and NHA1 knockout sperm, suggesting that the reduced motility and fertility is not due to deficient CatSper-mediated signaling [11]. Intriguingly, using Slo3 knockout or Lrrc52 knockout mice, both of which exhibit improperly depolarized E_m sperm phenotypes, it was shown that zona pellucida induced pH_i and Ca²⁺ responses were abolished [11]. Since Slo3 and Lrrc52 function together to establish a hyperpolarized membrane potential in capacitated sperm [70,71], this finding suggests that the pH_i and Ca²⁺ responses to zona pellucida proteins mediated by NHA1 requires a sufficiently negative E_m [11]. Zona pellucida proteins do not evoke an increase in cAMP synthesis, however cAMP synthesis by sAC is required upstream to prime NHA1 for activation in response to zona pellucida proteins [11]. How NHA1 is activated by zona pellucida proteins, E_m, or cAMP remains unknown and it is unclear if NHA1 plays a role in sperm physiology outside of zona pellucida induced alkalization.

4.3. NHA1 Transport Activity

To date, no mammalian NHA1 protein has been characterized with respect to transport activity, however the Drosophila melanogaster NHA1 protein is known to act as a Cl^-/H⁺ exchanger when expressed in Xenopus oocytes [75]. The Drosophila melanogaster NHA1 protein has been shown to be widely expressed across multiple tissues and its sequence is more similar to human NHA2 than human NHA1. Drosophila NHA1 activity is sensitive to the anion exchange inhibitors 4,4′-dibenzamido-2,2′-stilbenedisulphonate (DBDS) and 4,4′-diiso-thiocyano-2,2′-disulfonic acid stilbene (DIDS), but not to the NHE/Na⁺ channel inhibitor amiloride [75]. On the other hand, the Drosophila NHA2 protein sequence is more similar to that of the human NHA1 protein and Drosophila NHA2 was shown to be a functional NHE [75]. Knockdown of both NHA1 and NHA2 in Drosophila was lethal due to salt intolerance [75]. A recent study also characterized the activity of NHA1 from the red flour beetle, Tribolium castaneum, and found that this protein functions as an electroneutral H⁺/K⁺ antiporter [76]. However, Tribolium castaneum only possess one SLC9B gene homolog, and like Drosophila NHA1, the Tribolium NHA1 protein shares more sequence homology with mammalian NHA2 than NHA1. Therefore, direct comparison of the insect NHA proteins to mammalian NHA1 or NHA2 proteins should be undertaken with care and further research into directly characterizing the transport activity of mammalian NHA1 is of importance. However, the finding that NHA1 KO mice exhibit defects in pH_i regulation in response to zona pellucida stimulation strongly suggests that at least mouse NHA1 exhibits NHE activity (assuming that loss of NHA1 expression does not also result in loss of other pH regulating proteins) [11].

A structural model of human NHA1 was generated based on homology to bison NHA2 [77,78]. This human NHA1 model was overall identical to bison NHA2 and the structure of the ion-binding sites were identical. Importantly, the bison NHA2 has been shown to be a functional NHE (see NHA2 below) and all of the residues within the binding site with assigned roles for Na⁺ and H⁺ binding are also conserved in human NHA1. However, some residues proposed to function in phosphatidylinositol (PI) or phosphatidylinositol diphosphate (PIP₂) binding in bison NHA2 are not conserved in human NHA1. Additionally, human NHA1 possess different residues than those in bison NHA2 that are thought to be involved in the cytoplasmic dimerization interface. All of this data suggests that human NHA1 and bison NHA2 likely possess similar ion transport (NHE) activity, but may be regulated differently through their interaction with lipids and the stability of the dimer interface itself [77].

4.4. NHA1 and Human Fertility

NHA1 has been shown to be expressed in human testis via western blotting and immunohistochemistry [67]. Additionally, immunofluorescence revealed that NHA1 localizes to the principal piece in human sperm, the same localization as seen in mouse sperm [10]. NHA1 has also been reported to be present in the human sperm proteome [62]. Finally, a bioinformatics study examining recent population-specific positive directional selection of human male reproductive genes found that the SLC9B1 gene is under positive directional selection in all studied human populations. [79]. Taken together, these findings suggests that NHA1 is likely important for human male fertility however more work is needed to elucidate the specific role of this NHE in human sperm.

5. SLC9B2 (NHA2/NHEDC2)

5.1. Molecular Genetics and Expression Patterns

The SLC9B2 gene is located in tandem with the SLC9B1 gene on human Chromosome 4 and is comprised of 13 exons. In contrast to SLC9B1, the SLC9B2 gene exhibits near ubiquitous expression, including expression in testis and sperm, in both mouse and human [6,10,80,81]. In mature mouse sperm, NHA2 has been reported to reside in the membrane of the principal piece. [10].

NHA2 subcellular location seems to be widespread as it has been reported to localize to multiple cellular compartments in various cells. In mouse pancreatic β-cells, NHA2 localizes to endosomes and synaptic-like microvesicles and, similarly, was found to localize to late endosomes and lysosomes in mouse osteoclasts [82,83]. NHA2 is also reported to localize to mitochondria in both mouse osteoclasts and rat kidney cells [80,84]. Additionally, NHA2 was reported to localize to the plasma membrane of mouse kidney cells, mouse osteoclasts, and MDCK cells (canine kidney cells) [81,83,85,86].

Physiologically, NHA2 has been shown to be important for osteoclast function, insulin secretion, and nephron function where it has been implicated in playing a significant role in maintaining salt balance to support normotension [81,82,83,87]. NHA2 was reported to localize to the distal convoluted tubules of mouse kidney cells, and subcellularly found to localize to endosomes in mpkDCT4 cells, a mouse distal convoluted tubule epithelial cell line, although NHA2 was found to not influence endosomal pH homeostasis [87]. NHA2 knockout mice display a Gitelman syndrome-like phenotype, characterized by reduced blood pressure, normocalcemic hypocalciuria, and increased urinary aldosterone excretion. Mechanistically, NHA2 appears to regulate blood pressure through a WNK4-NCC pathway in the mouse kidney [87]. For a review on NHA2 work from the Reymond, von Ballmoos, and Fuster groups, see [88].

5.2. Sperm Physiology and Fertility

As with NHA1, two lines of NHA2 KO mice have been generated. The Liu group generated conditional NHA2 knockout mice in the same manner as the NHA1 conditional knockout mice [10] such that a conditional global knockout of NHA2 occurred. The NHA2 conditional knockout (NHA2 cKO) mice exhibited a very similar phenotype to the NHA1 cKO mice in that they were subfertile due to reduced sperm motility. Like the NHA1 cKO mice, there are no grossly abnormal testis or sperm morphologies and the sperm have reduced cAMP levels and sAC protein levels. Unfortunately, there is no information available regarding whether cAMP analogs can restore motility and fertility of NHA2 cKO sperm. Of interest, the NHA1 cKO mouse testis had significantly upregulated NHA2 mRNA and the NHA2 cKO mouse testis have significantly upregulated NHA1 mRNA, suggesting the functional redundancy for the two transporters [10]. Interestingly, there are no reports of a subfertile male phenotype from the second group that generated NHA2 knockout mice [82,87].

NHA1/NHA2 double knockout mice (NHA1/2 dKO) were reported to have been generated [10] however, as noted by [77] the likelihood of generating these NHA1/2 dKO [77] by cross-breeding the NHA1 cKO and NHA2 cKO mice is low because the SLC9B1 and SLC9B2 genes are located in tandem on chromosome 3 in mice. These two genes are separated by less than 18,500bp on mouse chromosome 3 (according to the chromosomal locations for these two genes provided in [64]), making the occurrence of a crossover event happening that would result in positioning both of the individual knockout alleles on the same chromosome extremely rare. Therefore, it would be expected to take a cumbersomely large number of matings between the single KO mice to generate the NHA1/2 dKO founder and thus the actual genotypes of the NHA1/2 dKO animals used in these studies are unclear. In any case, the NHA1/2 dKO sperm were reported to have almost no motility resulting in completely infertile males. Likely because the NHA1/2 dKO mouse sperm were reported to have significantly reduced cAMP and sAC protein levels [10]. Like with the NHA2 cKO sperm, there is no information about the ability of cAMP analogs to restore motility to the NHA1/2 dKO sperm. The authors of these studies suggested that NHA1 and NHA2 may be good targets for a male contraceptive drug due to their role in male fertility in mice [10], however, since NHA2 is ubiquitously expressed, developing a drug to target both proteins without having off-target effects may be difficult.

5.3. NHA2 Transport Activity

Initial attempts to characterize the transport activity of the human NHA2 protein found that heterologous expressed NHA2 in salt-sensitive yeast strains was able to transport either Na⁺ or Li⁺, consistent with conventional Na⁺/H⁺ exchanger activity [80,89]. Later characterization of human NHA2 was accomplished by overexpressing green fluorescent protein (GFP)-tagged human NHA2 fusion protein in MDCK cells and found that NHA2 acts to export Li⁺ out of the cell in exchange for the import of Na⁺, however in the presence of a high extracellular proton concentration (acidic conditions outside the cell) NHA2 could mediate Li⁺ efflux in exchange for H⁺ import. This NHA2 activity was inhibited by cytosolic acidification as no Na⁺ influx was seen after the cells were acid loaded [85]. In addition, there appears to be a consensus that NHA2 does not transport K⁺ and that its activity is not electrogenic [80,85,90]. Furthermore, NHA2 activity is resistant to amiloride but sensitive to the sodium-glucose transporter inhibitor phloretin [81,85]. Interestingly, exogenously expressed NHA2 coimmunoprecipitated with the V-type H⁺-ATPase in a kidney cell line and the V-type H⁺-ATPases inhibitor bafilomycin was able to block NHA2-mediated Li⁺ tolerance [85]. These findings led to a model proposing that NHA2 cation extrusion is driven by the proton gradient setup by the H⁺ efflux driven by the V-type H⁺-ATPase [85], therefore suggesting that human NHA2 is a H⁺-driven cation (Na⁺/Li⁺) exporter with activity similar to the prokaryotic NHAs. It is currently unclear whether NHA2 and V-Type H⁺-ATPases are also functionally coupled in spermatozoa, future experiments are needed to examine whether these proteins share similar transport characteristics in sperm and kidney cells.

More recent experiments found that human NHA2 preferentially forms stable homodimers in membranes [91] and exhibits electroneutral NHE activity when in proteoliposomes [90]. In addition, the structure of the bison NHA2 protein was recently solved and found to possess 14 transmembrane domains and form a homodimer [78]. Solid-state membrane-based electrophysiology experiments on proteoliposome-reconstituted bison NHA2 revealed that bison NHA2 mediates Na⁺/H⁺ exchange (can also transport Li⁺/H⁺) but in a pH dependent manner, specifically Na⁺(Li⁺)/H⁺ exchange was severely inhibited by a low pH outside the liposome relative to inside the liposomes. All together, these findings suggest that NHA2 operates as an electroneutral exchanger to drive Na⁺ efflux [78]. However, biochemical analyses of NHA2 in its native environment is lacking and whether or not NHA2 plays a role in organellar pH homeostasis such as endosomal pH regulation needs to be clarified. Also, how NHA2 transport activity influences sperm physiology remains unknown.

5.4. NHA2 and Human Fertility

There is currently no information available on the expression of NHA2 in human sperm nor of its contribution to human male fertility.

6. SLC9A1 (NHE1)

6.1. Molecular Genetics and Expression Patterns

The SLC9A1 gene is located on human Chromosome 1 and is comprised of 12 exons [92]. Due in part to its near ubiquitous expression pattern, NHE1 is often referred to as the “housekeeping” NHE involved in pH homeostasis and cell tonicity [6]. NHE1 has been shown to localize to various subregions of the plasma membrane in different cell types and in response to various stimuli. For example NHE1 localizes to caveolae and other cholesterol enriched microdomains, such as lipid rafts [6,93,94].

6.2. Sperm Physiology and Fertility

NHE1 localizes to the midpiece in mature rat and mouse sperm ([48] and our unpublished observations) and has also been shown to localize to both the equatorial region of the sperm head and to the sperm flagellum in ram and pig sperm [95,96]. Homozygous knockout of NHE1 (NHE1 KO) in mice results in ataxia, growth retardation and seizures evident around 2 weeks of age [7]. Due to repeated seizures, most NHE1 KO mice die before reaching sexual maturity, limiting the investigation of NHE1’s role in sperm physiology. Despite these limitations, NHE1 KO male mice that do reach sexual maturity are capable of siring offspring with wild type and NHE1 heterozygous knockout female mice. However, NHE1 KO X NHE1 KO mating results in an absence of offspring [7]. This suggests a potential reproductive issue with female NHE1 KO mice but no further research on the sperm physiology of NHE1 KO mice has been reported. Nonetheless, because NHE1 KO male mice do produce offspring with wild type and NHE1 heterozygous knockout females, this suggests that NHE1 is not critical for sperm physiology as complete loss of NHE1 in males does not alter murine fertility.

6.3. NHE1 Transport Activity

The mature NHE1 protein localizes to the plasma membrane and preferentially homodimerizes but only one functional copy of the dimer is needed for effective Na⁺/H⁺ exchange at an acidic pH [97,98]. The human NHE1 protein structure was recently solved by co-expressing NHE1 and the obligate binding partner calcineurin B-homologous protein 1 (CHP1) in HEK293 cells, and then reconstituting the NHE1-CHP1 complex in lipid nandodiscs and determining its structure by cryoelectron microscopy (cryo-EM) [47]. Human NHE1 was found to possess 13 transmembrane domains [47]. The intracellular C-terminus of the NHE1 protein acts as a pH sensor to allow for appropriate regulation of NHE activity, possibly through dimeric interaction between the C-termini of interacting NHE1 molecules [99,100]. NHE1 transport activity has been extensively characterized and it has been shown to exhibit either 1:1 or 2:2 stoichiometric exchange of extracellular Na⁺ for intracellular H⁺ [101,102] and is able to exchange in reverse mode if the ion gradients are reversed [103]. Of potential interest in the context of sperm physiology due to the importance of Ca²⁺ during capacitation, a human NHE1-Calmodulin (CaM) complex was solved by NMR and found that NHE1 transport activity is regulated both by CaM and intracellular Ca²⁺ concentrations [104]. However, it should be noted that NHE1 has been found to be regulated by CaM differently in different cell-specific and NHE1 phosphorylation state-specific manners [104,105,106,107], and therefore how or if NHE1 activity is regulated by Ca²⁺, CaM binding, or phosphorylation in in mammalian sperm is currently unknown but is a relevant future area of research.

NHE1 activity is highly sensitive to amiloride, ethylisopropoylamiloride (EIPA), 5-(N,N-dimethyl)-amiloride (DMA), and 5-(N,N-hexamethylene)-amiloride (HMA), and cariporide, all known inhibitors of NHEs (for reviews of NHE inhibitor structures, specificity and applications see) [6,7,108,109,110,111,112]. For a detailed review on NHE1 structure and transport see [113].

6.4. NHE1 and Human Fertility

Mass spectroscopy analysis revealed that NHE1 is present in the mature human sperm proteome [114], however no studies on the contribution of human NHE1 to male fertility exist. Several clinical studies have characterized homozygous mutations in the human SLC9A1 gene which result in loss of function of the NHE1 protein due to improper protein transport/exchange [115,116,117]. These patients suffer from ataxia or other CNS deficiencies [115,116,117], however fertility phenotypes associated with loss of human NHE1 activity have not been reported.

7. SLC9A3 (NHE3)

7.1. Molecular Genetics and Expression Patterns

The SLC9A3 gene is located on human chromosome 5 and is comprised of 17 exons. The NHE3 protein is most highly expressed within the digestive tract and kidney with expression in other tissues, including testis. NHE3 is known to undergo regulated insertion and retrieval between the plasma membrane and recycling endosomes, depending on the cellular context [6]. It is believed that NHE3 is either directly or indirectly responsible for the majority of the absorption of ingested Na⁺ in the small and large intestines as well as reabsorbing over half of the filtered Na⁺ in the proximal tubules of the kidneys [118]. For a detailed review on the role of NHE3 in the digestive tract and kidney, see [118].

7.2. Sperm Physiology and Fertility

NHE3 was first reported to be expressed in the male reproductive tract in the efferent duct and proximal regions of the epididymis in rat [119] and the efferent duct in human [120] and mice [121]. NHE3 KO male mice are infertile due to an abnormally dilated lumen of the rete testis and efferent tubules resulting in obstructive azoospermia [121,122]. Further analyses revealed that this phenotype is likely due to the significant decrease in transmembrane conductance regulator (CFTR) protein expression in the epididymis and vas deferens of NHE3 KO mice [123]. NHE3 and CFTR are known to interact in various cellular contexts [124,125], and therefore it is thought that the NHE3 KO phenotype is at least partially due to the loss of CFTR activity [123], as CFTR KO mice also display a similar male infertility phenotype [126,127].

NHE3 has also been shown to be expressed in spermiogenic cells in mouse testis, and found to specifically localize to the developing acrosomal granule [40]. Interestingly, NHE3 KO male mice produce sperm with severe acrosome defects, suggesting that NHE3 protein expression is essential for proper acrosome biogenesis. It should be noted that NHE3 has not been reported to be expressed in mature murine sperm. All of this data on NHE3 KO mice makes it clear that NHE3 expression is important for male fertility, both due to its role in acrosome biogenesis and its role in maintaining proper luminal fluid homeostasis in the epididymis and vas deferens [40,121,122,123]. However, whether NHE3 plays a functional role in mature sperm has yet to be reported.

7.3. NHE3 Transport Activity

The transport activity of the NHE3 protein has been extensively characterized via heterologous expression of NHE3 cDNA in cell culture systems. Rat NHE3 cDNA expressed recombinantly in an NHE-deficient cell line was found to function as an electroneutral NHE. When comparing rat NHE1 with rat NHE3 activity, it was found that NHE3 exhibits a higher affinity for Na⁺ than NHE1 but a lower affinity for H⁺. Additionally, NHE3 is significantly less sensitive to amiloride inhibition than NHE1 [110,128]. Potentially relevant to sperm physiology, NHE3 transport is decreased in response to increases in intracellular cAMP concentrations; cAMP activates PKA which leads to phosphorylation of serine residues within the cytoplasmic C-terminus of NHE3 to inhibit its activity [129,130,131]. How and if NHE3 is also inhibited via cAMP in testis or sperm is unknown, but would be functionally relevant. For a detailed review on regulatory binding partners and complexes of NHE3, see [132].

The structure of the human NHE3 protein was recently solved by co-expressing human NHE3 with human CHP1 and then the NHE3-CHP1 complex was reconstituted into nanodiscs and resolved with cryo-EM (in a similar manner to how the NHE1-CHP1 complex was solved) [133]. Results of this study show that NHE3 assembles as a homodimer, with each NHE3 monomer containing 13 transmembrane domains. This study also found that CHP1 co-expression enhances NHE3 trafficking to the plasma membrane and subsequently increased its transport activity. Additionally, NHE3 possesses an autoinhibitory domain, referred to as a plug motif, formed from a cytosolic helix-loop-helix motif that is thought to compete with substrate binding to inhibit transport. This autoinhibitory domain of NHE3 is apparently modulated by binding of auxiliary proteins or by phosphorylation to prevent or destabilize this autoinhibition, allowing for fine-tuning of NHE3 transport activity under specific cellular conditions [133].

7.4. NHE3 and Human Fertility

Human males with SLC9A3 mutations resulting in loss of NHE3 expression exhibit a congenital bilateral absence of the vas deferens (CBAVD) phenotype, reminiscent of the phenotype of the NHE3 KO mice [123,134]. Whether or not NHE3 is also expressed in human testis and sperm, specifically the developing acrosome, has yet to be reported. Therefore, NHE3’s role in human spermatogenesis is unclear, however the phenotype of the SLC9A3 mutant males demonstrates the importance for this NHE for proper male fertility due to its posited role in maintaining proper fluid homeostasis in the vas deferens.

8. SLC9A5 (NHE5)

8.1. Molecular Genetics and Expression Patterns

The SLC9A5 gene is located on human Chromosome 16 and is comprised of 16 exons. The NHE5 protein is predicted to be most similar to the NHE3 protein by sequence analysis and like NHE3, has been shown to localize to both the plasma membrane and recycling endosomes [6,135]. Analysis of mouse, rat, and human tissue RNA expression revealed NHE5 is most highly expressed in the brain, with second highest expression found in the testis and low levels expressed in various other tissues such as spleen and lung [6,136,137].

8.2. Sperm Physiology and Fertility

NHE5, along with NHE1, is localized to the midpiece of the sperm flagellum in rats and mice ([48] and our unpublished observations). An NHE5 knockout mouse model was generated and these mice display increases in memory and learning [138]. While the interest of this study was not the of the role of NHE5 in the sperm, the authors did report that the NHE5 KO mice displayed no fertility issues, suggesting that NHE5 may not be an essential protein for male fertility in mice. Future studies using these NHE5 knockout mice as a model to investigate specific aspects of male fertility such as motility, capacitation, and fertilization would be of great interest to further elucidate the role of NHE5 in mammalian sperm. Further, since NHE1 and NHE5 both localize to the midpiece of the sperm and therefore could compensate for each other, studies of NHE1/NHE5 double knockout mice may be needed to uncover the role of these two NHE subfamily members in these cells.

8.3. NHE5 Transport Activity

NHE5 cDNAs cloned from rat and human brain expressed in NHE-deficient cells were used to characterize NHE5 transport activity. Both rat and human NHE5 exhibit similar transport kinetics to NHE3 in that NHE5 is able to regulate pH_i by exchanging extracellular Na⁺ for intracellular H⁺, likely in an electroneutral manner [137,139]. Interestingly, rat NHE5 is inhibited by acute exposure to the cell permeant, non-hydrolysable cAMP analog 8-bromo-cAMP or to forskolin (which stimulates adenylate cyclase to synthesize cAMP), while the PKA inhibitor H-89 is able to prevent this cAMP-mediated NHE5 inhibition. The PKC activator phorbol 12-myristrate 13-acetate inhibits rat NHE5 while the PKC antagonist chelerythrine chloride blunts this effect [139]. Taken together, these findings suggest that both PKA and PKC act to inhibit rat NHE5 activity, although the mechanism behind this inhibition is currently unknown. A study using both neuronal and non-neuronal cells found that activated AMP-activated Protein Kinase (AMPK) phosphorylates human NHE5 which causes it to be recruited to the plasma membrane to regulate pH_i under specific conditions such as metabolic stress [140]. AMPK localizes to different parts of mature sperm in mouse, bull, and human, one location being the midpiece [141] where NHE5 is present in mice and rats. AMPK plays a role in energy homeostasis in mammalian sperm which directly contributes to sperm motility and thus fertility [141]. Additional studies are need to determine whether NHE5 is regulated by AMPK in the midpiece of mammalian sperm, if so, this could suggest a role for NHE5 in sperm energy homeostasis.

Both rat and human NHE5 activities are relatively insensitive to amiloride and slightly sensitive to EIPA, similar to the sensitivities of NHE3 to these NHE inhibitors [136,137,139]. Using these pharmacological inhibitors to understand the role of NHE5 activity in mammalian sperm is not possible because NHE5 is less sensitive to inhibition by them than is NHE1. Therefore, the higher inhibitor concentrations needed to block NHE5 activity will also inhibit NHE1 (as well as other potential Na⁺ transporters in sperm) and therefore any observed differences could not be attributed specifically to loss of NHE5 activity. It should be noted however, that incubating rat sperm with amiloride inhibits motility in a concentration-dependent manner (with an IC50 of 5X10^-5M) [2] suggesting that a relatively amiloride-resistant NHE (like NHE5) [112] may be involved.

8.4. NHE5 and Human Fertility

Nothing has been reported regarding NHE5 and human male reproduction other than a mass spectroscopy analysis which revealed the presence of NHE5 in mature human sperm [142]. Therefore, more work is needed to confirm NHE5’s presence in human sperm and to analyze its contribution to male fertility.

9. SLC9A8 (NHE8)

9.1. Molecular Genetics and Expression Patterns

The SLC9A8 gene is located on human Chromosome 20 and is comprised of 16 exons. The NHE8 protein is ubiquitously expressed and in somatic cells has been shown to localize to the trans-Golgi network and to function to regulate late endosomes by maintaining intra-Golgi pH [6,14,111,143]. In normal rat kidney (NRK) cells, the surface expression of NHE8 increases in response to acidic media via increased trafficking to the plasma membrane [144]. Thus, NHE8 displays roles in both the plasma membrane and intracellular compartments [6,43]. For a detailed review on NHE8, see [111].

9.2. Sperm Physiology and Fertility

NHE8 mRNA and protein have been reported to be expressed in both mouse and human testis and NHE8 protein was shown to be expressed in mouse and human Leydig cells and was shown to localize intracellularly in MLTC-1 cells (a mouse Leydig cell line) [145].

Two separate groups have independently generated NHE8 knockout mice and both groups report that male NHE8 knockout mice are completely infertile [9,145,146]. The first of these knockout mouse studies found that global knockout of NHE8 resulted in loss of sperm production due to impaired Leydig cell function [145]. The second NHE8 knockout mouse study found that both global knockout and germ-line specific knockout of NHE8 resulted in identical phenotypes; the NHE8 knockout sperm were round-headed, lacked acrosomes, and had incorrectly localized mitochondrial sheaths [9]. Sertoli cell specific NHE8 knockout resulted in mice with morphologically normal sperm that were fertile [9]. Importantly, this study also reports that NHE8 colocalizes with the acrosome during all stages of spermiogenesis in wildtype mouse [9]. Although both NHE8 knockout mouse studies resulted in infertile males, there seems to be some discrepancies between these studies. The Oberheide group appears to clearly show that NHE8 loss-mediated infertility comes from a germ cell specific origin and that NHE8 expression is present in developing wildtype mouse spermatozoa, which the Xu group does not report. Also, the Oberheide group reports an absence of any NHE8 expression in Leydig cells thus the role of NHE8 in these cells is in question. Regardless of the discrepancies, both NHE8 knockout studies demonstrate that NHE8 is a vital protein to male fertility. Future research is needed to determine what the exact role of NHE8 is in acrosome formation during spermiogenesis and if NHE8 has a role in mature sperm during or after the acrosome reaction.

9.3. NHE8 Transport Activity

Initial cloning and expression of human NHE8 and subsequent reconstitution into proteoliposomes showed that NHE8 does possess Na⁺/H⁺ exchange activity [14]. Additionally, NHE8 was found to function as a NHE that is sensitive to EIPA however these experiments used EIPA concentrations that would also minimally inhibit NHE1 activity in AP-1 cells [147]. A recent study characterized the transport activity of both rat and human NHE8 in the NHE-deficient PS120 cell line, and found both rat and human NHE8 function as NHEs that are highly sensitive to the NHE1 inhibitor cariporide (HOE642) [148].

9.4. NHE8 and Human Fertility

Immunohistochemical labeling of NHE8 in the Leydig cells of human testis has been reported [145]. However, there is currently no data on the expression of NHE8 in human sperm or of its contribution to human male fertility. The phenotype of NHE8 knockout mouse sperm (rounded heads that lack acrosomes) is a very similar to the clinical condition of globozoospermia that affects some human males, suggesting that NHE8 may be a genetic candidate for clinical globozoospermia diagnosis [9].

10. Discussion

10.1. NHEs are essential for male fertility

As discussed, there is ample evidence suggesting that multiple NHEs are important for sperm function and male fertility. NHE3 is important for male fertility in mice due to its contribution in both acrosomal biogenesis in the testis [40] and its role in maintaining proper osmolarity in the efferent duct [121,122]. NHE8 has also shown to be essential for male mouse fertility with roles in both acrosomal biogenesis [9] and in Leydig cell function [145]. Male NHA1 knockout mice are subfertile due to reduced sperm motility [10,11] and this NHE is involved in the zona pellucida-induced alkalization observed in capacitated sperm where it functions downstream of CatSper, Slo3, and cAMP’s influence [11]. However, the NHE for which there is the most evidence for being critical for mammalian fertility is NHE10 [8,12,13,56] and therefore an expanded discussion of NHE10’s role in male fertility is warranted. In addition, because of the dependence of NHE activity on the Na⁺ gradient established by the Na,K-ATPase and the potential interaction between NHE10 and the SLO3 K⁺ channel, the CatSper Ca²⁺ channel, the Hv1 proton channel, the sAC protein, and cAMP, we will be discussing the role of these functionally connected proteins and signaling molecules in the greater context of sperm physiology.

10.2. NHE10/11’s likely functional dependence with SLO1/3-mediated hyperpolarization in mammalian sperm

Membrane hyperpolarization, as part of capacitation events, is of demonstrated importance for the fertilizing ability of both human and mouse sperm [23,26,27,70,149,150]. Human sperm that exhibit depolarized membrane potentials have low fertilization rates during IVF [151,152] and hyperpolarization after capacitation is a strong predictor for the acrosome reaction, hyperactivity, and successful IVF [26,27]. Using fluorimetry to measure human sperm membrane potential demonstrated that non-capacitating sperm have an average E_m of -37.7 ± 9.9 mV, while capacitated sperm have an E_m of -57.8 ± 12.9 mV [27]. Similarly, flow cytometry revealed that non-capacitated human sperm have an E_m of -35.7 ± 2.8 mV and capacitated sperm have an E_m of -45.2 ± 3.2 mV. Potentially more physiologically important, fertile human sperm have an E_m of -58.03 ± 3.00 mV while non-fertile sperm have an E_m of -40.61 ± 2.60 mV [26]. Although little is known about the activity of the mammalian SLC9C proteins, these E_m values of capacitated/fertile human sperm are consistent with values at which the suSLC9C protein has been shown to become active in the absence of cNMP (V_1/2 of -70.9 ± 2.5 mV) and in the presence of cAMP (V_1/2 of -56.8 ± 2.7 mV) [59]. This shift to a more depolarized activation of suSLC9C in the presence of cAMP suggests that the suSLC9C protein may only be active post capacitation, when cAMP levels rise due to sAC activity and the E_m hyperpolarizes. The transport activity of the mammalian SLC9C proteins (NHE10 and NHE11) have yet to be determined, however, if they share similar voltage and cyclic nucleotide regulation as their sea urchin orthologue, the NHE10/11 proteins could be responsible for pH regulation in mammalian sperm that have undergone membrane hyperpolarization in response to capacitating conditions.

Studies using Slo3 and NHE10 knockout animals support the idea that NHE10 regulates sperm pH_i in response to membrane hyperpolarization in mice. First, it appears that Slo3 K⁺ channels regulate Ca2⁺ entry via CatSper in mouse sperm through membrane hyperpolarization by regulating sperm K⁺ current (KSper); Slo3 KO mouse sperm do not display CatSper-mediated Ca²⁺ currents unless external pH is increased or the E_m is artificially hyperpolarized with an ionophore [23]. In addition, treatment of wildtype mouse sperm with valinomycin, a K⁺ selective ionophore which causes artificial hyperpolarization of the sperm E_m, induces a pH_i increase, further supporting that mouse sperm pH_i is regulated by membrane voltage change and led to the suggestion that a voltage dependent NHE (NHE10) may be responsible for activating CatSper in response to the hyperpolarization evoked from Slo3 channels opening [23]. Additional experiments found that when the inward Na⁺ gradient was depleted mouse sperm cells still undergo hyperpolarization but the CatSper mediated Ca²⁺ current is absent, further evidence supporting possible NHE activity in the activation of CatSper [23]. A recent study found that WT mouse sperm undergo cytosolic alkalization in the sperm flagellum under valinomycin-induced E_m hyperpolarization, but NHE10 KO mice do not [58], demonstrating that in mouse, NHE10 expression is required for the hyperpolarization-induced alkalization. Interestingly, simply incubating mouse sperm in alkaline conditions is able to activate Slo3 mediated hyperpolarization [153], suggesting that the journey through the female reproductive tract, in which the sperm encounter a progressively increasing external pH, may be enough to influence Slo3 channel activation and subsequent E_m hyperpolarization.

While human sperm also require membrane hyperpolarization to activate CatSper-mediated Ca²⁺ entry, unlike mouse sperm, they do not undergo cytosolic alkalization in response to valinomycin-induced hyperpolarization [58] suggesting that humans may have evolved a different role for their SLC9C proteins in sperm. In addition, the K⁺ channel responsible for Ca²⁺-mediated human sperm hyperpolarization is still not definitively identified [154]. It has been suggested that this channel could be SLO1 because SLO1 channels are Ca²⁺ sensitive while SLO3 are generally not [25]. It has also been suggested that SLO3 is responsible for the observed human sperm hyperpolarization because unlike mouse Slo3, human SLO3 is only weakly activated by an increase in pH_i, but strongly activated by an increase in Ca²⁺ from CatSper [24]. Both SLO1 and SLO3 are present in human sperm, and therefore it is unclear what each ion channel’s role is in sperm hyperpolarization, even though it is clear that K⁺ efflux (mediating membrane hyperpolarization) is important for human sperm capacitation and fertilization [74,150,155].

10.3. Interaction of NHEs and sAC in sperm

Cell-permeant, cAMP analogs restore motility and fertility to NHE10 KO sperm [56], NHE10 and sAC co-immunoprecipitate from mouse and sea urchin sperm [56,156], and in cultured cells, the heterologous expression of mouse sAC and NHE10 are mutually dependent [56] suggesting that these two proteins are functionally linked. Interestingly, in sea urchin sperm, sAC co-immunoprecipitates with the suSLC9C protein along with other known plasma membrane and axonemal proteins [156]. These findings suggest that in the sea urchin sperm flagellum, suSLC9C and sAC, along with multiple other proteins, form a large protein complex that would allow an increase in cAMP generated by sAC to efficiently shift the activation voltage of this NHE to a more positive, physiologically relevant V_m via interaction with the CNBD of the suSLC9C protein located in the same complex [59]. Mammalian NHE10 and NHE11 both are predicted to possess CNBDs with conserved residues important for cyclic nucleotide binding [8,42], and therefore are also equipped to be regulated by the increase in cAMP mediated by sAC stimulation in capacitation events.

10.4. Functional interdependence of CatSper and NHEs

As mentioned, the CatSper complex is responsible for the Ca²⁺ influx into the cell that is required for capacitation. Alkalization shifts the activation threshold of CatSper to more negative physiologically relevant potentials [28,29,69]. In mouse sperm, CatSper is activated by increases of pH_i and is E_m sensitive [28,32]. In human sperm, CatSper current is also E_m sensitive and is strongly activated by alkalization, however unlike in mouse sperm, progesterone enhances CatSper current without directly influencing pH_i [29,69,157]. The dependence of CatSper activation on pH_i increase strongly implicates the activity of pH regulating proteins, such as NHEs, in this process.

Interestingly, a comparative genomic study found that nearly all animals that possess CatSper genes also have both sAC and at least one SLC9C gene [46]. Species that do not have a sAC gene, do not have SLC9C or CatSper genes. On the other hand, the presence of SLC9B genes does not predict CatSper gene conservation. The authors suggest that this phylogenetic data is evidence that sAC, SLC9C, and CatSper are functionally intertwined [46].

When mouse sperm are treated with 5-(N,N-dimethyl)-amiloride (DMA), a potent inhibitor of NHEs, the cytoplasm acidifies and motility is reduced [33]. DMA was found not to affect KSper or CatSper directly, but patch clamp recordings found that DMA application resulted in both KSper and CatSper inhibition (when extracellular pH was at physiological levels and the pipette solutions were not buffered), leading to depolarization of the membrane potential and decreased intracellular Ca²⁺ levels. When pipette solutions were buffered, DMA did not have this effect, suggesting that the observed KSper and CatSper inhibition were direct results of the acidification due to NHE(s) inhibition. These results suggest that NHE activity is responsible for modulating proper KSper and CatSper activity under physiological conditions [33]. However, it is currently unclear which NHE(s) are being inhibited by DMA, therefore repeating these experiments with different NHE knockout mouse sperm could help uncover the specific NHE(s) involved. It has been noted that CatSper activity is unaffected in NHE10 KO mice [158] however, these experiments were performed with buffered pipette solutions, which would minimize any pH_i decrease that the NHE10 loss may have caused in the mouse sperm, leaving open the possibility that NHE10 activity helps modulate CatSper activity in mouse sperm [33].

10.5. NHEs versus Hv1 ion channel: determining the regulator of pH_i human sperm

The voltage-sensitive proton channel Hv1 is expressed at a high concentration in the principal piece of human sperm, and has been proposed to be the main membrane protein responsible for alkalizing these cells [159,160]. Hv1 only allows protons out of human sperm and Hv1 currents activate when the sperm membrane potential is set to 0 mV or greater under physiological pH conditions [159]. In addition, structural studies found that the Hv1 channel is open under depolarizing conditions and closed under hyperpolarized conditions [161]. Human sperm express both a full length Hv1 protein and a truncated Hv1 termed Hv1Sper, which is a post-translationally cleaved version of Hv1 missing the first 68 amino acids of the N-terminus [149]. Hv1Sper has reduced pH sensing and lower (less positive) activation currents (V_1/2) than Hv1. The Hv1 proton channel is not expressed in mouse sperm, which is likely why Hv1 knockout male mice are fertile [162,163]. Of note, studies suggesting that Hv1 is the major pH regulation use patch clamping of the sperm, which is only able to measure electrogenic currents, and therefore would not detect the activity of any electroneutral NHEs that are regulated by voltage.

Hv1 has recently been shown to be directly activated by albumin binding, and while the albumin concentration in human semen is too low to activate Hv1, the higher albumin concentration in the female reproductive tract is high enough to activate it [164]. Albumin binding shifts the activation threshold of Hv1 to a more negative physiologically relevant V_m, which helps explains how Hv1 could contribute to human sperm alkalization during the capacitation process [164]. Supporting its importance, inhibition of Hv1 results in a decrease in the percent of capacitated human sperm that were able to undergo the acrosome reaction and decreased CatSper-mediated Ca²⁺ influx [165]. All of this is strong evidence that efflux of H⁺ via Hv1 plays an important role in the sperm capacitation process in humans, however how the activity of NHEs fit in with Hv1 activity in human sperm physiology are still incompletely defined and an important future area of study.

Ionic conditions in the female reproductive tract seem to suggest an important role for NHE activity in sperm physiology; as the sperm exit the cauda epididymis, the [Na⁺] is <25 mM and the pH is <7 however as the sperm travel through the female reproductive tract, they encounter a higher [Na⁺] and more alkaline conditions [166]. In addition, capacitated human sperm have decreased pH_i when incubated in media that lacks extracellular Na⁺ [38,39], suggesting a role of NHE(s) in pH_i regulation of sperm. The human sperm head and principal piece, but apparently not the midpiece, alkalize in response to capacitation [19]. Based on their locations, this suggests that NHE1 and NHE5 may be responsible for maintaining basal pH regulation in the midpiece, while activation of NHE10, NHA1, or Hv1/Hv1Sper is responsible for alkalization in the principal piece. Since the sperm E_m hyperpolarizes after capacitation, it is likely increases in NHE10 activity that is responsible for the observed increased alkalization in the principal piece, at least in mice [58]. However, NHA1 activity has been shown to require a hyperpolarized E_m for activation in response to zona pellucida proteins [11], and therefore NHA1 may be playing a role similar to the role proposed for NHE10 in the principle piece. NHE11 is the only known NHE to localize to the head of mammalian sperm, and therefore it may be involved in regulating pH_i in the sperm head in response to capacitation.

The NHE inhibitor EIPA is able to inhibit pH_i regulation in capacitated human sperm [38], although it is unclear which NHE(s) EIPA inhibits in human sperm. EIPA has been shown to inhibit NHE1, and to a lesser degree NHE5, but it is unclear yet if EIPA inhibits mammalian NHA1, NHA2, NHE10, or NHE11 [7,108,137,147]. Interestingly, EIPA did not affect the ability of capacitated human sperm to undergo the acrosome reaction by progesterone stimulation, suggesting that EIPA-sensitive NHE activity is not essential for the acrosome reaction [38]. Knowing the relative contribution of each NHE to regulating human sperm pH_i during different physiological processes is important to understand the specialized functional roles of NHEs and Hv1; it is likely that multiple NHEs as well as Hv1 perform different functions in human sperm physiology, all of which are important for male fertility.

Interestingly, cell culture studies support the idea that Hv1 and NHE10 may have different cellular roles. Due to technical difficulties, it was necessary to measure NHE exchange in reverse in order to determine whether the VSD of the suSLC9C protein regulates its NHE activity. To overcome this, human Hv1 was co-transfected into the CHO cells and then NHE activity was measured in reverse exchange mode so that the suSLC9C protein would acidify the cell under hyperpolarized V_m conditions and then Hv1 would restore the original pH_i under depolarized V_m conditions. Therefore, when expressed in transfected cells, suSLC9C and human Hv1 are not active at the same V_m [59], suggesting potential functional differences for sperm physiology. However, because these experiments were performed in cell culture, applying these results to sperm cell physiology must be undertaken cautiously.

10.6. NHEs and the Functional Dependence on Na,K-ATPases

NHEs are thought to rely on the electrochemical gradient established by the Na,K-ATPase in sperm [48], and therefore the differential localization of the individual NHE isoforms and Na,K-ATPase alpha isoforms may suggest more specific functional dependence between individual isoforms of these proteins. Mammalian sperm express two different alpha Na,K-ATPase subunit isoforms (the alpha subunit is the enzymatically active subunit of the Na,K-ATPase), the alpha1 isoform and the alpha4 isoform. The alpha1 isoform localizes to the entire sperm flagellum in both rat and human [167,168]. The alpha4 isoform localizes to the midpiece of the sperm flagellum in rats [48,169] and has been reported to localize in human sperm to the principal piece [170], head and flagellum [171], and midpiece [168]. While there seems to be some discrepancy as to which specific subsection(s) the alpha4 isoform localizes to, it is clearly in the sperm flagellum. It would be interesting to see if either alpha1 or alpha4 differentially coimmunoprecipitate with any specific NHE isoforms in sperm, as this could suggest a specialized complex of functionally coupled transporters. Loss of the alpha4 isoform in mice results in male infertility due to abnormal Na⁺ regulation and depolarized membrane potential [172]. Plasma membrane alpha4 expression and activity were found to increase during capacitation in rat sperm [173]; alpha4 activity provides the Na⁺ gradient for NHE exchange while also hyperpolarizing the E_m, potentially setting the electrical gradient necessary for voltage sensitive NHEs. Future studies into the role of both the alpha1 and alpha4 Na,K-ATPase isoforms are necessary to examine their functional significance to NHEs in sperm. It should be noted that, since the transport activity of every NHE found in sperm has not been characterized, it is possible that some of them may not function as conventional NHEs (importing Na⁺ and exporting H⁺) and therefore may not rely on the electrochemical gradient established by Na,K-ATPase activity.

10.7. Importance of the Characterization of NHE Transport Activity in Sperm

To fully understand the contribution of each NHE to sperm physiology, it is imperative to characterize the NHE transport activity of each NHE in these cells. Although the transport activity of some NHEs have been characterized in vitro, it is possible (and highly likely), that these proteins exhibit different transport activity in sperm than they do when expressed in cultured cells. Therefore, it is of importance to characterize the activity of these NHEs in in vitro and in vivo assays, using combinations of heterologous expression in cultured cells, reconstitution of purified proteins in defined lipid environments, and NHE knockout mouse sperm models. Interestingly, out of all of the NHEs expressed in mammalian sperm, the only three that have yet to have their transport activities characterized to at least some degree in heterologous cell culture systems are those that display testis/sperm specific expression (NHA1, NHE10, and NHE11). Our experience suggests that it is extremely difficult to express these three NHEs in cell culture using known methodologies. In support of our observations, a recent study found that the VSD of NHE10 is highly toxic to both bacteria and cultured mammalian cells [174]. Thus, an effort to make novel gene-edited mouse models, such as those containing point mutations that would alter amino acids thought to be important for transport function, to characterize these proteins is essential to fully understand how each NHE contributes to sperm physiology.

In addition, NHE proteins are known to interact with and be modulated by several accessory proteins. Therefore, in the various NHE KO mouse models that exhibit male fertility defects, it is important to determine whether it is the loss of NHE transport activity that is responsible for the observed male infertility, or if it the loss/dysfunction of proteins that associate with that NHE that is responsible for the observed phenotype.

10.8. Models for NHE contribution to mammalian sperm physiology

While we recognize that many aspects of the intricate signaling pathways remain to be elucidated, especially in human sperm, we present here a potential working model for NHE activity in mammalian sperm physiology. Immediately following ejaculation into the vagina, various NHEs in the flagellum and potentially Hv1/Hv1Sper (in the principal piece of human sperm) participate in maintaining a basal pH under non-capacitating conditions. As sperm leave the vagina and enter the cervix to continue along the reproductive tract, they are exposed to signaling molecules and changing ionic concentrations which favor capacitation. As the sperm encounter a higher extracellular Na⁺ concentration, basal NHE activity (potentially due to multiple NHEs) in the midpiece and principal piece increases. This increase in sperm intracellular pH (as well as exposure to increasingly alkaline pH environment in the female reproductive tract) activates Slo3 in mouse sperm which causes an efflux of K⁺ and hyperpolarization of the sperm E_m. The hyperpolarization of the E_m via Slo3 is necessary in mouse sperm prior to CatSper activation, but in human sperm, SLO3 is strongly activated by Ca²⁺; progesterone-activated CatSper activity is enough to activate SLO3. Therefore, it is currently unclear what the order of SLO3 and CatSper activation in human sperm is. In mouse sperm, the hyperpolarization caused by Slo3 activation activates NHE10 activity, which causes an increase in pH_i, further activating Slo3, therefore these two proteins act to positively regulate each other once one is activated. This mutual NHE10-SLO3 activation can explain two hallmarks of sperm capacitation: sperm membrane hyperpolarization and an increase in sperm pH_i. All the while, Na,K-ATPases are continuously active in order to establish and maintain the Na⁺ and K⁺ gradients used by NHE10 and Slo3. The increase in pH_i, due to NHE activity, activates CatSper, resulting in transient Ca²⁺ influx which finely controls capacitation associated events such as sAC synthesis of cAMP - sAC activity is activated both by Ca²⁺ and HCO₃^-. The increase in cAMP leads to activation of PKA and sets off a signaling cascade ultimately resulting in an increase in pY. The sperm hyperpolarization and increase in intracellular cAMP achieved in capacitation acts to prime mouse sperm for exposure to zona pellucida proteins from the oocyte. The zona pellucida proteins activate NHA1 to further alkalize the cell, again activating CatSper to mediate Ca²⁺ influx and initiate additional signaling events for fertilization of the egg. The exact start of capacitation events in human sperm and the role that NHEs play is more enigmatic because human SLO3 is activated more strongly by Ca²⁺ than pH_i. Therefore, it is possible that CatSper activation via progesterone (released from the oocyte) precedes SLO3 and NHE10 activation in human sperm. It is also unclear whether NHA1 plays the same role in zona pellucida induced alkalization in humans as it does in mice.

Figure 5. Signaling pathways in mammalian sperm flagellum. A) Mouse sperm flagellum signaling involving NHEs. ZP stands for zona pellucida protein. B) Human sperm flagellum signaling involving NHEs. See text for details. Solid arrows indicated literature validated mechanisms. Faded arrows indicate proposed or putative mechanisms. pY stands for phosphorylated-tyrosine protein levels. Cartoon created with Biorender.com.

11. Conclusion

NHEs are important for male fertility in many species, spanning sea urchins to humans. There are currently 8 known NHEs that are expressed in mammalian testis/sperm, however the exact role of each of these NHEs in male fertility remains to be determined. Future work is needed to characterize the transport activity of all of these NHEs in a testis/sperm-specific context. Of particular interest is further characterization of the human NHE10 and NHE11 proteins because of their potential regulation by voltage and cyclic nucleotides which are known to be important for capacitated sperm and NHE10 has also been shown to be essential for male fertility. NHE10 has been shown to be essential for human male fertility and exhibits testis/sperm-specific expression and is therefore an attractive target for male contraceptive drugs. An exciting area of future research, NHE11 specifically localizes to the sperm head, the only NHE known to do so in rodent and human sperm. Although its contribution to male fertility is unknown, NHE11 transport activity is also likely regulated by E_m and cyclic nucleotides, and its unique localization positions it to potentially regulate important sperm physiology events such as the acrosome reaction or sperm-egg fusion/fertilization events. Finally, investigating all of the NHEs expressed in sperm will give us a better understanding of the intricacies of ion transport and regulation involved in male reproductive biology as well potentially identifying abnormalities that affect some human males currently suffering from infertility.

Author Contributions

Conceptualization, C.C.G. and P.F.J.; formal analysis, C.C.G. and P.F.J.; investigation, C.C.G. and P.F.J.; resources, P.F.J.; writing—original draft preparation, C.C.G. and P.F.J.; writing—review and editing, C.C.G. and P.F.J.; visualization, C.C.G.; supervision, P.F.J.; funding acquisition, P.F.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research reported in this paper was supported by funds from Miami University and from the National Institute of Child Health and Human Development (NICHD) of the National Institutes of Health under award number R15HD101985.

Acknowledgements

We would like to thank Jason A. Abele for helping carefully review this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

Orlowski, J.; Grinstein, S. Diversity of the Mammalian Sodium/Proton Exchanger SLC9 Gene Family. Pflugers Arch. Eur. J. Physiol. 2004, 447, 549–565. [Google Scholar] [CrossRef] [PubMed]
Wong, P.Y.D.; Lee, W.M.; Tsang, A.Y.F. The Effects of Extracellular Sodium on Acid Release and Motility Initiation in Rat Caudal Epididymal Spermatozoa in Vitro. Exp. Cell Res. 1981, 131, 97–104. [Google Scholar] [CrossRef] [PubMed]
Yun, C.H.C.; Tse, C.M.; Nath, S.K.; Levine, S.A.; Brant, S.R.; Donowitz, M. Mammalian Na+/H+ Exchanger Gene Family: Structure and Function Studies. Am. J. Physiol. - Gastrointest. Liver Physiol. 1995, 269. [Google Scholar] [CrossRef]
Counillon, L.; Pouysségur, J. The Expanding Family of Eucaryotic Na+/H+ Exchangers. J. Biol. Chem. 2000, 275, 1–4. [Google Scholar] [CrossRef] [PubMed]
Donowitz, M.; Ming Tse, C.; Fuster, D. SLC9/NHE Gene Family, a Plasma Membrane and Organellar Family of Na +/H+ Exchangers. Mol. Aspects Med. 2013, 34, 236–251. [Google Scholar] [CrossRef] [PubMed]
Pedersen, S.F.; Counillon, L. The SLC9A-C Mammalian Na+/H+ Exchanger Family: Molecules, Mechanisms, and Physiology. Physiol. Rev. 2019, 99, 2015–2113. [Google Scholar] [CrossRef]
Bell, S.M.; Schreiner, C.M.; Schultheis, P.J.; Miller, M.L.; Evans, R.L.; Vorhees, C. V.; Shull, G.E.; Scott, W.J. Targeted Disruption of the Murine Nhe1 Locus Induces Ataxia, Growth Retardation, and Seizures. Am. J. Physiol. - Cell Physiol. 1999, 276. [Google Scholar] [CrossRef]
Wang, D.; King, S.M.; Quill, T.A.; Doolittle, L.K.; Garbers, D.L. A New Sperm-Specific Na+/H+ Exchanger Required for Sperm Motility and Fertility. Nat. Cell Biol. 2003, 5, 1117–1122. [Google Scholar] [CrossRef]
Oberheide, K.; Puchkov, D.; Jentsch, T.J. Loss of the Na+/H+ Exchanger NHE8 Causes Male Infertility in Mice by Disrupting Acrosome Formation. J. Biol. Chem. 2017, 292, 10845–10854. [Google Scholar] [CrossRef]
Chen, S.R.; Chen, M.; Deng, S.L.; Hao, X.X.; Wang, X.X.; Liu, Y.X. Sodium–Hydrogen Exchanger NHA1 and NHA2 Control Sperm Motility and Male Fertility. Cell Death Dis. 2016, 7, e2152-9. [Google Scholar] [CrossRef]
Balbach, M.; Hamzeh, H.; Jikeli, J.F.; Brenker, C.; Schiffer, C.; Hansen, J.N.; Neugebauer, P.; Trötschel, C.; Jovine, L.; Han, L.; et al. Molecular Mechanism Underlying the Action of Zona-Pellucida Glycoproteins on Mouse Sperm. Front. Cell Dev. Biol. 2020, 8, 1–15. [Google Scholar] [CrossRef]
Zhang, Z.; Yang, Y.; Wu, H.; Zhang, H.; Zhang, H.; Mao, J.; Liu, D.; Zhao, L.; Lin, H.C.; Tang, W.; et al. Sodium-Hydrogen-Exchanger Expression in Human Sperm and Its Relationship with Semen Parameters. J. Assist. Reprod. Genet. 2017, 34, 795–801. [Google Scholar] [CrossRef]
Cavarocchi, E.; Whitfield, M.; Chargui, A.; Stouvenel, L.; Coutton, C.; Arnoult, C.; Santulli, P.; Patrat, C.; Ray, P.F.; Dulioust, E.; et al. The Sodium/Proton Exchanger SLC9C1 (SNHE) Is Essential for Human Sperm Motility and Fertility. Clin. Genet. 2021. [Google Scholar] [CrossRef]
Nakamura, N.; Tanaka, S.; Teko, Y.; Mitsui, K.; Kanazawa, H. Four Na+/H+ Exchanger Isoforms Are Distributed to Golgi and Post-Golgi Compartments and Are Involved in Organelle PH Regulation. J. Biol. Chem. 2005, 280, 1561–1572. [Google Scholar] [CrossRef]
Chang, M. Fertilizing Capacity of Spermatozoa Deposited into the Fallopian Tubes. Nature 1951, 168, 697–698. [Google Scholar] [CrossRef] [PubMed]
Babcock, D.F.; Rufo, G.; Lardy, H.A. Potassium-Dependent Increases in Cytosolic PH Stimulate Metabolism and Motility of Mammalian Sperm. Proc. Natl. Acad. Sci. U. S. A. 1983, 80, 1327–1331. [Google Scholar] [CrossRef]
Vijayaraghavan, S.; Critchlow, L.M.; Hoskins, D.D. Evidence for a Role for Cellular Alkalinization in the Cyclic Adenosine 3’,5’-Monophosphate-Mediated Initiation of Motility in Bovine Caput Spermatozoa. Biol. Reprod. 1985, 32, 489–500. [Google Scholar] [CrossRef]
Carr, D.W.; Acott, T.S. Intracellular PH Regulates Bovine Sperm Motility and Protein Phosphorylation. Biol. Reprod. 1989, 920, 907–920. [Google Scholar]
Matamoros-Volante, A.; Trevino, C.L. Capacitation-Associated Alkalization in Human Sperm Is Differentially Controlled at the Subcellular Level. J. Cell Sci. 2020, 133. [Google Scholar] [CrossRef]
Visconti, P.E.; Bailey, J.L.; Moore, G.D.; Pan, D.; Olds-Clarke, P.; Kopf, G.S. Capacitation of Mouse Spermatozoa. Development 1995, 121, 1129–1137. [Google Scholar]
Wertheimer, E.; Krapf, D.; De La Vega-Beltran, J.L.; Sánchez-Cárdenas, C.; Navarrete, F.; Haddad, D.; Escoffier, J.; Salicioni, A.M.; Levin, L.R.; Buck, J.; et al. Compartmentalization of Distinct CAMP Signaling Pathways in Mammalian Sperm. J. Biol. Chem. 2013, 288, 35307–35320. [Google Scholar] [CrossRef] [PubMed]
Xie, F.; Garcia, M.A.; Carlson, A.E.; Schuh, S.M.; Babcock, D.F.; Jaiswal, B.S.; Gossen, J.A.; Esposito, G.; van Duin, M.; Conti, M. Soluble Adenylyl Cyclase (SAC) Is Indispensable for Sperm Function and Fertilization. Dev. Biol. 2006, 296, 353–362. [Google Scholar] [CrossRef]
Chávez, J.C.; Ferreira, J.J.; Butler, A.; De La Vega Beltrán, J.L.; Treviño, C.L.; Darszon, A.; Salkoff, L.; Santi, C.M. SLO3 K+ Channels Control Calcium Entry through CATSPER Channels in Sperm. J. Biol. Chem. 2014, 289, 32266–32275. [Google Scholar] [CrossRef]
Brenker, C.; Zhou, Y.; Müller, A.; Echeverry, F.A.; Trötschel, C.; Poetsch, A.; Xia, X.M.; Bönigk, W.; Lingle, C.J.; Kaupp, U.B.; et al. The Ca2+-Activated K+ Current of Human Sperm Is Mediated by Slo3. Elife 2014, 2014, 1–19. [Google Scholar] [CrossRef]
Mannowetz, N.; Naidoo, N.M.; Choo, S.-A.S.; Smith, J.F.; Lishko, P. V Slo1 Is the Principal Potassium Channel of Human Spermatozoa. Elife 2013, 2, 1–19. [Google Scholar] [CrossRef]
Molina, L.C.P.; Gunderson, S.; Riley, J.; Lybaert, P.; Borrego-Alvarez, A.; Jungheim, E.S.; Santi, C.M. Membrane Potential Determined by Flow Cytometry Predicts Fertilizing Ability of Human Sperm. Front. Cell Dev. Biol. 2020, 7, 1–12. [Google Scholar] [CrossRef]
Baro Graf, C.; Ritagliati, C.; Torres-Monserrat, V.; Stival, C.; Carizza, C.; Buffone, M.G.; Krapf, D. Membrane Potential Assessment by Fluorimetry as a Predictor Tool of Human Sperm Fertilizing Capacity. Front. Cell Dev. Biol. 2020, 7, 1–10. [Google Scholar] [CrossRef]
Kirichok, Y.; Navarro, B.; Clapham, D.E. Whole-Cell Patch-Clamp Measurements of Spermatozoa Reveal an Alkaline-Activated Ca2+ Channel. Nature 2006, 439, 737–740. [Google Scholar] [CrossRef]
Strünker, T.; Goodwin, N.; Brenker, C.; Kashikar, N.D.; Weyand, I.; Seifert, R.; Kaupp, U.B. The CatSper Channel Mediates Progesterone-Induced Ca2+ Influx in Human Sperm. Nature 2011, 471, 382–387. [Google Scholar] [CrossRef]
Nishigaki, T.; José, O.; González-Cota, A.L.; Romero, F.; Treviño, C.L.; Darszon, A. Intracellular PH in Sperm Physiology. Biochem. Biophys. Res. Commun. 2014, 450, 1149–1158. [Google Scholar] [CrossRef]
Lee, H.C. A Membrane Potential-Sensitive Na+-H+ Exchange System in Flagella Isolated from Sea Urchin Spermatozoa. J. Biol. Chem. 1984, 259, 15315–15319. [Google Scholar] [CrossRef] [PubMed]
Hwang, J.Y.; Mannowetz, N.; Zhang, Y.; Everley, R.A.; Gygi, S.P.; Bewersdorf, J.; Lishko, P. V.; Chung, J.J. Dual Sensing of Physiologic PH and Calcium by EFCAB9 Regulates Sperm Motility. Cell 2019, 177, 1480–1494.e19. [Google Scholar] [CrossRef] [PubMed]
Kang, H.; Liu, M.; Zhang, W.; Huang, R.Z.; Zhao, N.; Chen, C.; Zeng, X.H. Na+/H+ Exchangers Involve in Regulating the Ph-Sensitive Ion Channels in Mouse Sperm. Int. J. Mol. Sci. 2021, 22, 1–13. [Google Scholar] [CrossRef]
Gunderson, S.J.; Puga Molina, L.C.; Spies, N.; Balestrini, P.A.; Buffone, M.G.; Jungheim, E.S.; Riley, J.; Santi, C.M. Machine-Learning Algorithm Incorporating Capacitated Sperm Intracellular PH Predicts Conventional in Vitro Fertilization Success in Normospermic Patients. Fertil. Steril. 2021, 1–9. [Google Scholar] [CrossRef]
Keskes, L.; Giroux-Widemann, V.; Serres, C.; Pignot-Paintrand, I.; Jouannet, P.; Feneux, D. The Reactivation of Demembranated Human Spermatozoa Lacking Outer Dynein Arms Is Independent of PH. Mol. Reprod. Dev. 1998, 49, 416–425. [Google Scholar] [CrossRef]
Hansbrough, J.R.; Garbers, D.L. Sodium-Dependent Activation of Sea Urchin Spermatozoa by Speract and Monensin. J. Biol. Chem. 1981, 256, 2235–2241. [Google Scholar] [CrossRef] [PubMed]
Gatti, J.L.; Christen, R. Regulation of Internal PH of Sea Urchin Sperm. J. Biol. Chem. 1985, 260, 7599–7602. [Google Scholar] [CrossRef]
Garcia, M.A.; Meizel, S. Regulation of Intracellular PH in Capacitated Human Spermatozoa by a Na+/H+ Exchanger. Mol. Reprod. Dev. 1999, 52, 189–195. [Google Scholar] [CrossRef]
Garcia, M.A.; Meizel, S. Importance of Sodium Ion to the Progesterone-Initiated Acrosome Reaction in Human Sperm. Mol. Reprod. Dev. 1996, 45, 513–520. [Google Scholar] [CrossRef]
Wang, Y.Y.; Chiang, H.S.; Cheng, C.Y.; Wu, Y.N.; Lin, Y.C.; Liu, H.C.; Tsai, W.K.; Chen, Y.L.; Lin, Y.H. SLC9A3 Protein Is Critical for Acrosomal Formation in Postmeiotic Male Germ Cells. Int. J. Mol. Sci. 2018, 19. [Google Scholar] [CrossRef]
Letunic, I.; Bork, P. Interactive Tree of Life (ITOL) v4: Recent Updates and New Developments. Nucleic Acids Res. 2019, 47, 256–259. [Google Scholar] [CrossRef]
Gardner, C.C.; James, P.F. The SLC9C2 Gene Product ( Na + / H + Exchanger Isoform 11 ; NHE11 ) Is a Testis-Specific Protein Localized to the Head of Mature Mammalian Sperm. Int. J. Mol. Sci. 2023, 24. [Google Scholar] [CrossRef]
Brett, C.L.; Donowitz, M.; Rao, R. Evolutionary Origins of Eukaryotic Sodium/Proton Exchangers. Am. J. Physiol. - Cell Physiol. 2005, 288. [Google Scholar] [CrossRef]
Taglicht, D.; Padan, E.; Schuldiner, S. Proton-Sodium Stoichiometry of NhaA, an Electrogenic Antiporter from Escherichia Coli. J. Biol. Chem. 1993, 268, 5382–5387. [Google Scholar]
Pinner, E.; Padan, E.; Schuldiner, S. Kinetic Properties of NhaB, a Na+/H+ Antiporter from Escherichia Coli. J. Biol. Chem. 1994, 269, 26274–26279. [Google Scholar]
Romero, F.; Nishigaki, T. Comparative Genomic Analysis Suggests That the Sperm-Specific Sodium/Proton Exchanger and Soluble Adenylyl Cyclase Are Key Regulators of CatSper among the Metazoa. Zool. Lett. 2019, 5, 1–12. [Google Scholar] [CrossRef]
Dong, Y.; Gao, Y.; Ilie, A.; Kim, D.S.; Boucher, A.; Li, B.; Zhang, X.C.; Orlowski, J.; Zhao, Y. Structure and Mechanism of the Human NHE1-CHP1 Complex. Nat. Commun. 2021, 12. [Google Scholar] [CrossRef]
Woo, A.L.; James, P.F.; Lingrel, J.B. Roles of the Na,K-ATPase A4 Isoform and the Na+/H+ Exchanger in Sperm Motility. Mol. Reprod. Dev. 2002, 62, 348–356. [Google Scholar] [CrossRef] [PubMed]
Izadyar, F.; Wong, J.; Maki, C.; Pacchiarotti, J.; Ramos, T.; Howerton, K.; Yuen, C.; Greilach, S.; Zhao, H.H.; Chow, M.; et al. Identification and Characterization of Repopulating Spermatogonial Stem Cells from the Adult Human Testis. Hum. Reprod. 2011, 26, 1296–1306. [Google Scholar] [CrossRef] [PubMed]
Zhang, L.; Tang, J.; Haines, C.J.; Feng, H.; Lai, L.; Teng, X.; Han, Y. C-Kit and Its Related Genes in Spermatogonial Differentiation. Spermatogenesis 2011, 1, 186–194. [Google Scholar] [CrossRef]
Unni, S.K.; Modi, D.N.; Pathak, S.G.; Dhabalia, J. V.; Bhartiya, D. Stage-Specific Localization and Expression of c-Kit in the Adult Human Testis. J. Histochem. Cytochem. 2009, 57, 861–869. [Google Scholar] [CrossRef]
Helsel, A.R.; Yang, Q.E.; Oatley, M.J.; Lord, T.; Sablitzky, F.; Oatley, J.M. Id4 Levels Dictate the Stem Cell State in Mouse Spermatogonia. Dev. 2017, 144, 624–634. [Google Scholar] [CrossRef]
Robertson, M.J.; Kent, K.; Tharp, N.; Nozawa, K.; Dean, L.; Mathew, M.; Grimm, S.L.; Yu, Z.; Légaré, C.; Fujihara, Y.; et al. Large-Scale Discovery of Male Reproductive Tract-Specific Genes through Analysis of RNA-Seq Datasets. BMC Biol. 2020, 18, 1–28. [Google Scholar] [CrossRef]
Cavarocchi, E.; Whitfield, M.; Chargui, A.; Stouvenel, L.; Lorès, P.; Coutton, C.; Arnoult, C.; Santulli, P.; Patrat, C.; Thierry-Mieg, N.; et al. The Sodium/Proton Exchanger SLC9C1 (SNHE) Is Essential for Human Sperm Motility and Fertility. Clin. Genet. 2021, 99, 684–693. [Google Scholar] [CrossRef] [PubMed]
Gardner, C.C.; Abele, J.A.; Winkler, T.J.; Reckers, C.N.; Anas, S.A.; James, P.F. Common as Well as Unique Methylation-Sensitive DNA Regulatory Elements in Three Mammalian SLC9C1 Genes. bioRxiv 2023. [Google Scholar] [CrossRef]
Wang, D.; Hu, J.; Bobulescu, I.A.; Quill, T.A.; McLeroy, P.; Moe, O.W.; Garbers, D.L. A Sperm-Specific Na+/H+ Exchanger (SNHE) Is Critical for Expression and in Vivo Bicarbonate Regulation of the Soluble Adenylyl Cyclase (SAC). Proc. Natl. Acad. Sci. U. S. A. 2007, 104, 9325–9330. [Google Scholar] [CrossRef]
Jansen, V.; Alvarez, L.; Balbach, M.; Strünker, T.; Hegemann, P.; Kaupp, U.B.; Wachten, D. Controlling Fertilization and CAMP Signaling in Sperm by Optogenetics. Elife 2015, 2015, 1–15. [Google Scholar] [CrossRef]
Hernández-Garduño, S.; Chávez, J.C.; Matamoros-Volante, A.; Sánchez-Guevara, Y.; Torres, P.; Treviño, C.L.; Nishigaki, T. Hyperpolarization Induces Cytosolic Alkalization of Mouse Sperm Flagellum Probably through Sperm Na+/H+ Exchanger. Reproduction 2022, 164, 125–134. [Google Scholar] [CrossRef] [PubMed]
Windler, F.; Bönigk, W.; Körschen, H.G.; Grahn, E.; Strünker, T.; Seifert, R.; Kaupp, U.B. The Solute Carrier SLC9C1 Is a Na+/H+-Exchanger Gated by an S4-Type Voltage-Sensor and Cyclic-Nucleotide Binding. Nat. Commun. 2018, 9, 1–13. [Google Scholar] [CrossRef]
Lee, H.C.; Garbers, D.L. Modulation of the Voltage-Sensitive Na+/H+ Exchange in Sea Urchin Spermatozoa through Membrane Potential Changes Induced by the Egg Peptide Speract. J. Biol. Chem. 1986, 261, 16026–16032. [Google Scholar] [CrossRef]
Trötschel, C.; Hamzeh, H.; Alvarez, L.; Pascal, R.; Lavryk, F.; Bönigk, W.; Körschen, H.G.; Müller, A.; Poetsch, A.; Rennhack, A.; et al. Absolute Proteomic Quantification Reveals Design Principles of Sperm Flagellar Chemosensation. EMBO J. 2020, 39, 1–18. [Google Scholar] [CrossRef]
Urizar-Arenaza, I.; Osinalde, N.; Akimov, V.; Puglia, M.; Candenas, L.; Pinto, F.M.; Muñoa-Hoyos, I.; Gianzo, M.; Matorras, R.; Irazusta, J.; et al. Phosphoproteomic and Functional Analyses Reveal Sperm-Specific Protein Changes Downstream of Kappa Opioid Receptor in Human Spermatozoa. Mol. Cell. Proteomics 2019, 18, S118–S131. [Google Scholar] [CrossRef] [PubMed]
Vandenbrouck, Y.; Lane, L.; Carapito, C.; Duek, P.; Rondel, K.; Bruley, C.; Macron, C.; Gonzalez De Peredo, A.; Couté, Y.; Chaoui, K.; et al. Looking for Missing Proteins in the Proteome of Human Spermatozoa: An Update. J. Proteome Res. 2016, 15, 3998–4019. [Google Scholar] [CrossRef] [PubMed]
Holmes, R.S.; Spradling-Reeves, K.D.; Cox, L.A. Evolution of Vertebrate Solute Carrier Family 9B Genes and Proteins (SLC9B): Evidence for a Marsupial Origin for Testis Specific SLC9B1 from an Ancestral Vertebrate SLC9B2 Gene. J Phylogenetics Evol Biol 2016, 4. [Google Scholar] [CrossRef]
Liu, T.; Huang, J.C.; Zuo, W.L.; Lu, C.L.; Chen, M.; Zhang, X. Sen; Li, Y.C.; Cai, H.; Zhou, W.L.; Hu, Z.Y.; et al. A Novel Testis-Specific Na+/H+ Exchanger Is Involved in Sperm Motility and Fertility. Front. Biosci. - Elit. 2010, 2 E, 566–581. [Google Scholar] [CrossRef]
Ye, G.; Chen, C.; Han, D.; Xiong, X.; Kong, Y.; Wan, B.; Yu, L. Cloning of a Novel Human NHEDC1 (Na+/H+ Exchanger like Domain Containing 1) Gene Expressed Specifically in Testis. Mol. Biol. Rep. 2006, 33, 175–180. [Google Scholar] [CrossRef]
Kumar, P.L.; James, P.F. Identification and Characterization of Methylation-Dependent/ Independent DNA Regulatory Elements in the Human SLC9B1 Gene. Gene 2015, 561, 235–248. [Google Scholar] [CrossRef]
Liu, T.; Huang, J.C.; Lu, C.L.; Yang, J.L.; Hu, Z.Y.; Gao, F.; Liu, Y.X. Immunization with a DNA Vaccine of Testis-Specific Sodium-Hydrogen Exchanger by Oral Feeding or Nasal Instillation Reduces Fertility in Female Mice. Fertil. Steril. 2010, 93, 1556–1566. [Google Scholar] [CrossRef]
Lishko, P. V.; Botchkina, I.L.; Kirichok, Y. Progesterone Activates the Principal Ca2+ Channel of Human Sperm. Nature 2011, 471, 387–392. [Google Scholar] [CrossRef]
Santi, C.M.; Martínez-López, P.; de la Vega-Beltrán, J.L.; Butler, A.; Alisio, A.; Darszon, A.; Salkoff, L. The SLO3 Sperm-Specific Potassium Channel Plays a Vital Role in Male Fertility. FEBS Lett. 2010, 584, 1041–1046. [Google Scholar] [CrossRef] [PubMed]
Zeng, X.H.; Yang, C.; Xia, X.M.; Liua, M.; Lingle, C.J. SLO3 Auxiliary Subunit LRRC52 Controls Gating of Sperm KSPER Currents and Is Critical for Normal Fertility. Proc. Natl. Acad. Sci. U. S. A. 2015, 112, 2599–2604. [Google Scholar] [CrossRef]
Yang, C.; Zeng, X.H.; Zhou, Y.; Xia, X.M.; Lingle, C.J. LRRC52 (Leucine-Rich-Repeat-Containing Protein 52), a Testis-Specific Auxiliary Subunit of the Alkalization-Activated Slo3 Channel. Proc. Natl. Acad. Sci. U. S. A. 2011, 108, 19419–19424. [Google Scholar] [CrossRef] [PubMed]
Lyon, M.; Li, P.; Ferreira, J.J.; Lazarenko, R.M.; Kharade, S. V.; Kramer, M.; McClenahan, S.J.; Days, E.; Bauer, J.A.; Spitznagel, B.D.; et al. A Selective Inhibitor of the Sperm-Specific Potassium Channel SLO3 Impairs Human Sperm Function. Proc. Natl. Acad. Sci. 2023, 120. [Google Scholar] [CrossRef] [PubMed]
Lv, M.; Liu, C.; Ma, C.; Yu, H.; Shao, Z.; Gao, Y.; Liu, Y.; Wu, H.; Tang, D.; Tan, Q.; et al. Homozygous Mutation in SLO3 Leads to Severe Asthenoteratozoospermia Due to Acrosome Hypoplasia and Mitochondrial Sheath Malformations. Reprod. Biol. Endocrinol. 2022, 20, 1–15. [Google Scholar] [CrossRef]
Chintapalli, V.R.; Kato, A.; Henderson, L.; Hirata, T.; Woods, D.J.; Overend, G.; Davies, S.A.; Romero, M.F.; Dow, J.A.T. Transport Proteins NHA1 and NHA2 Are Essential for Survival, but Have Distinct Transport Modalities. Proc. Natl. Acad. Sci. U. S. A. 2015, 112, 11720–11725. [Google Scholar] [CrossRef]
Naseem, M.T.; Beaven, R.; Koyama, T.; Naz, S.; Su, S.; Leader, D.P.; A. Klaerke, D.; Calloe, K.; Denholm, B.; Halberg, K. V. NHA1 Is a Cation/Proton Antiporter Essential for the Water-Conserving Functions of the Rectal Complex in Tribolium Castaneum. Proc. Natl. Acad. Sci. 2023, 120, 2017. [Google Scholar] [CrossRef]
Anderegg, M.A.; Gyimesi, G.; Ho, T.M.; Hediger, M.A.; Fuster, D.G. The Less Well-Known Little Brothers: The SLC9B/NHA Sodium Proton Exchanger Subfamily—Structure, Function, Regulation and Potential Drug-Target Approaches. Front. Physiol. 2022, 13, 1–15. [Google Scholar] [CrossRef]
Matsuoka, R.; Fudim, R.; Jung, S.; Zhang, C.; Bazzone, A.; Chatzikyriakidou, Y.; Robinson, C. V.; Nomura, N.; Iwata, S.; Landreh, M.; et al. Structure, Mechanism and Lipid-Mediated Remodeling of the Mammalian Na+/H+ Exchanger NHA2. Nat. Struct. Mol. Biol. 2022, 29, 108–120. [Google Scholar] [CrossRef]
Schaschl, H.; Wallner, B. Population-Specific, Recent Positive Directional Selection Suggests Adaptation of Human Male Reproductive Genes to Different Environmental Conditions. BMC Evol. Biol. 2020, 20, 1–11. [Google Scholar] [CrossRef]
Fuster, D.G.; Zhang, J.; Shi, M.; Alexandru Bobulescu, I.; Andersson, S.; Moe, O.W. Characterization of the Sodium/Hydrogen Exchanger NHA2. J. Am. Soc. Nephrol. 2008, 19, 1547–1556. [Google Scholar] [CrossRef]
Xiang, M.; Feng, M.; Muend, S.; Rao, R. A Human Na+/H+ Antiporter Sharing Evolutionary Origins with Bacterial NhaA May Be a Candidate Gene for Essential Hypertension. Proc. Natl. Acad. Sci. U. S. A. 2007, 104, 18677–18681. [Google Scholar] [CrossRef]
Deisl, C.; Simonin, A.; Anderegg, M.; Albano, G.; Kovacs, G.; Ackermann, D.; Moch, H.; Dolci, W.; Thorens, B.; Hediger, M.A.; et al. Sodium/Hydrogen Exchanger NHA2 Is Critical for Insulin Secretion in β-Cells. Proc. Natl. Acad. Sci. U. S. A. 2013, 110, 10004–10009. [Google Scholar] [CrossRef]
Hofstetter, W.; Siegrist, M.; Simonin, A.; Bonny, O.; Fuster, D.G. Sodium/Hydrogen Exchanger NHA2 in Osteoclasts: Subcellular Localization and Role in Vitro and in Vivo. Bone 2010, 47, 331–340. [Google Scholar] [CrossRef]
Battaglino, R.A.; Pham, L.; Morse, L.R.; Vokes, M.; Sharma, A.; Odgren, P.R.; Yang, M.; Sasaki, H.; Stashenko, P. NHA-Oc/NHA2: A Mitochondrial Cation-Proton Antiporter Selectively Expressed in Osteoclasts. Bone 2008, 42, 180–192. [Google Scholar] [CrossRef] [PubMed]
Kondapalli, K.C.; Kallay, L.M.; Muszelik, M.; Rao, R. Unconventional Chemiosmotic Coupling of NHA2, a Mammalian Na +/H+ Antiporter, to a Plasma Membrane H+ Gradient. J. Biol. Chem. 2012, 287, 36239–36250. [Google Scholar] [CrossRef] [PubMed]
Kondapalli, K.C.; Todd Alexander, R.; Pluznick, J.L.; Rao, R. NHA2 Is Expressed in Distal Nephron and Regulated by Dietary Sodium. J. Physiol. Biochem. 2017, 73, 199–205. [Google Scholar] [CrossRef]
Anderegg, M.A.; Albano, G.; Hanke, D.; Deisl, C.; Uehlinger, D.E.; Brandt, S.; Bhardwaj, R.; Hediger, M.A.; Fuster, D.G. The Sodium/Proton Exchanger NHA2 Regulates Blood Pressure through a WNK4-NCC Dependent Pathway in the Kidney. Kidney Int. 2021, 99, 350–363. [Google Scholar] [CrossRef]
Ho, T.M.; Berger, S.; Müller, P.; Simonin, C.; Reymond, J.; Von Ballmoos, C.; Fuster, D.G. Physiological and Molecular Function of the Sodium/Hydrogen Exchanger NHA2 (SLC9B2). Chimia (Aarau). 2022, 76, 1019. [Google Scholar] [CrossRef]
Huang, X.; Morse, L.R.; Xu, Y.; Zahradka, J.; Sychrová, H.; Stashenko, P.; Fan, F.; Battaglino, R.A. Mutational Analysis of NHAoc/NHA2 in Saccharomyces Cerevisiae. Biochim. Biophys. Acta - Gen. Subj. 2010, 1800, 1241–1247. [Google Scholar] [CrossRef]
Uzdavinys, P.; Coinçon, M.; Nji, E.; Ndi, M.; Winkelmann, I.; Von Ballmoos, C.; Drew, D. Dissecting the Proton Transport Pathway in Electrogenic Na+/H+ Antiporters. Proc. Natl. Acad. Sci. U. S. A. 2017, 114, E1101–E1110. [Google Scholar] [CrossRef] [PubMed]
Landreh, M.; Marklund, E.G.; Uzdavinys, P.; Degiacomi, M.T.; Coincon, M.; Gault, J.; Gupta, K.; Liko, I.; Benesch, J.L.P.; Drew, D.; et al. Integrating Mass Spectrometry with MD Simulations Reveals the Role of Lipids in Na+/H+ Antiporters. Nat. Commun. 2017, 8. [Google Scholar] [CrossRef]
Miller, R.T.; Counillon, L.; Pages, G.; Lifton, R.P.; Sardet, C.; Pouyssegur, J. Structure of the 5’-Flanking Regulatory Region and Gene for the Human Growth Factor-Activatable Na/H Exchanger NHE-1. J. Biol. Chem. 1991, 266, 10813–10819. [Google Scholar] [CrossRef]
Bullis, B.L.; Li, X.; Rieder, C. V.; Singh, D.N.; Berthiaume, L.G.; Fliegel, L. Properties of the Na+/H+ Exchanger Protein Detergent-Resistant Aggregation and Membrane Microdistribution. Eur. J. Biochem. 2002, 269, 4887–4895. [Google Scholar] [CrossRef] [PubMed]
Tekpli, X.; Huc, L.; Lacroix, J.; Rissel, M.; Poët, M.; Noël, J.; Dimanche-Boitrel, M.T.; Counillon, L.; Lagadic-Gossmann, D. Regulation of Na+/H+ Exchanger 1 Allosteric Balance by Its Localization in Cholesterol- and Caveolin-Rich Membrane Microdomains. J. Cell. Physiol. 2008, 216, 207–220. [Google Scholar] [CrossRef] [PubMed]
Yeste, M.; Recuero, S.; Maside, C.; Salas-Huetos, A.; Bonet, S.; Pinart, E. Blocking Nhe Channels Reduces the Ability of in Vitro Capacitated Mammalian Sperm to Respond to Progesterone Stimulus. Int. J. Mol. Sci. 2021, 22. [Google Scholar] [CrossRef]
Muzzachi, S.; Guerra, L.; Martino, N.A.; Favia, M.; Punzi, G.; Silvestre, F.; Guaricci, A.C.; Roscino, M.T.; Pierri, C.L.; Elena, M.; et al. Effect of Cariporide on Ram Sperm PH Regulation and Motility: Possible Role of NHE1. Reproduction 2018. [Google Scholar]
Fafournoux, P.; Noël, J.; Pouysségur, J. Evidence That Na+/H+ Exchanger Isoforms NHE1 and NHE3 Exist as Stable Dimers in Membranes with a High Degree of Specificity for Homodimers. J. Biol. Chem. 1994, 269, 2589–2596. [Google Scholar]
Hisamitsu, T.; Ben Ammar, Y.; Nakamura, T.Y.; Wakabayashi, S. Dimerization Is Crucial for the Function of the Na+/H + Exchanger NHE1. Biochemistry 2006, 45, 13346–13355. [Google Scholar] [CrossRef]
Wakabayashi, S.; Fafournoux, P.; Sardet, C.; Pouysségur, J. The Na+/H+ Antiporter Cytoplasmic Domain Mediates Growth Factor Signals and Controls “H+-Sensing. ” Proc. Natl. Acad. Sci. U. S. A. 1992, 89, 2424–2428. [Google Scholar] [CrossRef] [PubMed]
Hisamitsu, T.; Pang, T.; Shigekawa, M.; Wakabayashi, S. Dimeric Interaction between the Cytoplasmic Domains of the Na +/H+ Exchanger NHE1 Revealed by Symmetrical Intermolecular Cross-Linking and Selective Co-Immunoprecipitation. Biochemistry 2004, 43, 11135–11143. [Google Scholar] [CrossRef]
Paris, S.; Pouyssegur, J. Biochemical Characterization of the Amiloride-Sensitive Na +/ H + Antiport in Chinese Hamster Lung Fibroblasts. J. Biol. Chem. 1982, 258, 3503–3508. [Google Scholar]
Fuster, D.; Moe, O.W.; Hilgemann, D.W. Steady-State Function of the Ubiquitous Mammalian Na/H Exchanger (NHE1) in Relation to Dimer Coupling Models with 2Na/2H Stoichiometry. J. Gen. Physiol. 2008, 132, 465–480. [Google Scholar] [CrossRef] [PubMed]
Grinstein, S.; Goetz, J.D.; Rothstein, A. 22Na+ Fluxes in Thymic Lymphocytes: II. Amiloride-Sensitive Na+/H+ Exchange Pathway; Reversibility of Transport and Asymmetry of the Modifier Site. J. Gen. Physiol. 1984, 84, 585–600. [Google Scholar] [CrossRef]
Sjøgaard-Frich, L.M.; Prestel, A.; Pedersen, E.S.; Severin, M.; Kristensen, K.K.; Olsen, J.G.; Kragelund, B.B.; Pedersen, S.F.; Kay, L.E. Dynamic Na+/H+ Exchanger 1 (NHE1) - Calmodulin Complexes of Varying Stoichiometry and Structure Regulate Ca2+-Dependent NHE1 Activation. Elife 2021, 10, 1–29. [Google Scholar] [CrossRef]
Snabaitis, A.K.; Cuello, F.; Avkiran, M. Protein Kinase B/Akt Phosphorylates and Inhibits the Cardiac Na+/H+ Exchanger NHE1. Circ. Res. 2008, 103, 881–890. [Google Scholar] [CrossRef]
Meima, M.E.; Webb, B.A.; Witkowska, H.E.; Barber, D.L. The Sodium-Hydrogen Exchanger NHE1 Is an Akt Substrate Necessary for Actin Filament Reorganization by Growth Factors. J. Biol. Chem. 2009, 284, 26666–26675. [Google Scholar] [CrossRef] [PubMed]
Wakabayashi, S.; Ikeda, T.; Iwamoto, T.; Pouysségur, J.; Shigekawa, M. Calmodulin-Binding Autoinhibitory Domain Controls “PH-Sensing” in the Na + /H + Exchanger NHE1 through Sequence-Specific Interaction. Biochemistry 1997, 36, 12854–12861. [Google Scholar] [CrossRef]
Kleyman, T.R.; Cragoe, E.J. Amiloride and Its Analogs as Tools in the Study of Ion Transport. J. Membr. Biol. 1988, 105, 1–21. [Google Scholar] [CrossRef]
Mihaila, R.G. A Minireview on NHE1 Inhibitors. A Rediscovered Hope in Oncohematology. Biomed. Pap. 2015, 159, 519–526. [Google Scholar] [CrossRef]
Counillon, L.; Scholz, W.; Lang, H.J.; Pouysségur, J. Pharmacological Characterization of Stably Transfected Na / H Antiporter Isoforms Using Amiloride Analogs and a New Inhibitor Properties. Mol. Pharmacol. 1993, 1041–1045. [Google Scholar]
Bernardazzi, C.; Sheikh, I.A.; Xu, H.; Ghishan, F.K. The Physiological Function and Potential Role of the Ubiquitous Na+/H+ Exchanger Isoform 8 (NHE8): An Overview Data. Int. J. Mol. Sci. 2022, 23. [Google Scholar] [CrossRef]
Masereel, B.; Pochet, L.; Laeckmann, D. An Overview of Inhibitors of Na+/H+ Exchanger. Eur. J. Med. Chem. 2003, 38, 547–554. [Google Scholar] [CrossRef]
Poet, M.; Doyen, D.; Van Obberghen, E.; Jarretou, G.; Bouret, Y.; Counillon, L. How Does Our Knowledge on the Na+/H+ Exchanger NHE1 Obtained by Biochemical and Molecular Analyses Keep up With Its Recent Structure Determination? Front. Physiol. 2022, 13, 1–12. [Google Scholar] [CrossRef]
Wang, G.; Guo, Y.; Zhou, T.; Shi, X.; Yu, J.; Yang, Y.; Wu, Y.; Wang, J.; Liu, M.; Chen, X.; et al. In-Depth Proteomic Analysis of the Human Sperm Reveals Complex Protein Compositions. J. Proteomics 2013, 79, 114–122. [Google Scholar] [CrossRef] [PubMed]
Guissart, C.; Li, X.; Leheup, B.; Drouot, N.; Montaut-Verient, B.; Raffo, E.; Jonveaux, P.; Roux, A.F.; Claustres, M.; Fliegel, L.; et al. Mutation of SLC9A1, Encoding the Major Na+/H+ Exchanger, Causes Ataxia-Deafness Lichtenstein-Knorr Syndrome. Hum. Mol. Genet. 2015, 24, 463–470. [Google Scholar] [CrossRef] [PubMed]
Iwama, K.; Osaka, H.; Ikeda, T.; Mitsuhashi, S.; Miyatake, S.; Takata, A.; Miyake, N.; Ito, S.; Mizuguchi, T.; Matsumoto, N. A Novel SLC9A1 Mutation Causes Cerebellar Ataxia. J. Hum. Genet. 2018, 63, 1049–1054. [Google Scholar] [CrossRef] [PubMed]
Fliegel, L. Role of Genetic Mutations of the Na+/H+ Exchanger Isoform 1, in Human Disease and Protein Targeting and Activity. Mol. Cell. Biochem. 2020. [Google Scholar] [CrossRef]
Nwia, S.M.; Li, X.C.; Leite, A.P. de O.; Hassan, R.; Zhuo, J.L. The Na+/H+ Exchanger 3 in the Intestines and the Proximal Tubule of the Kidney: Localization, Physiological Function, and Key Roles in Angiotensin II-Induced Hypertension. Front. Physiol. 2022, 13. [Google Scholar] [CrossRef]
Physiol, A.J.; Physiol, R.; Joseph, A.; Shur, B.D.; Hess, R.A.; Bagnis, C.; Marsolais, M.; Biemesderfer, D.; Laprade, R.; Schaeffer, D.J.; et al. Na + / H + -Exchange Activity and Immunolocalization of NHE3 in Rat Epididymis Na ϩ / H ϩ -Exchange Activity and Immunolocalization of NHE3 in Rat Epididymis. Ren. Physiol. 2011.
Hihnala, S.; Kujala, M.; Toppari, J.; Kere, J.; Holmberg, C.; Höglund, P. Expression of SLC26A3, CFTR and NHE3 in the Human Male Reproductive Tract: Role in Male Subfertility Caused by Congenital Chloride Diarrhoea. Mol. Hum. Reprod. 2006, 12, 107–111. [Google Scholar] [CrossRef]
Zhou, Q.; Clarke, L.; Nie, R.; Carnes, K.; Lai, L.W.; Lien, Y.H.H.; Verkman, A.; Lubahn, D.; Fisher, J.S.; Katzenellenbogen, B.S.; et al. Estrogen Action and Male Fertility: Roles of the Sodium/Hydrogen Exchanger-3 and Fluid Reabsorption in Reproductive Tract Function. Proc. Natl. Acad. Sci. U. S. A. 2001, 98, 14132–14137. [Google Scholar]
Schultheis, P.J.; Clarke, L.L.; Meneton, P.; Miller, M.L.; Soleimani, M.; Gawenis, L.R.; Riddle, T.M.; Duffy, J.J.; Doetschman, T.; Wang, T.; et al. Renal and Intestinal Absorptive Defects in Mice Lacking the NHE3 Na+/H+ Exchanger. Nat. Genet. 1998, 19, 282–285. [Google Scholar] [CrossRef]
Wang, Y.Y.; Lin, Y.H.; Wu, Y.N.; Chen, Y.L.; Lin, Y.C.; Cheng, C.Y.; Chiang, H.S. Loss of SLC9A3 Decreases CFTR Protein and Causes Obstructed Azoospermia in Mice. PLoS Genet. 2017, 13, 1–19. [Google Scholar] [CrossRef]
Ahn, W.; Kim, K.H.; Lee, J.A.; Kim, J.Y.; Choi, J.Y.; Moe, O.W.; Milgram, S.L.; Muallem, S.; Lee, M.G. Regulatory Interaction between the Cystic Fibrosis Transmembrane Conductance Regulator and HCO3- Salvage Mechanisms in Model Systems and the Mouse Pancreatic Duct. J. Biol. Chem. 2001, 276, 17236–17243. [Google Scholar] [CrossRef] [PubMed]
Bagorda, A.; Guerra, L.; Sole, F. Di; Hemle-Kolb, C.; Cardone, R.A.; Fanelli, T.; Reshkin, S.J.; Gisler, S.M.; Murer, H.; Casavola, V. Reciprocal Protein Kinase A Regulatory Interactions between Cystic Fibrosis Transmembrane Conductance Regulator and Na+/H+ Exchanger Isoform 3 in a Renal Polarized Epithelial Cell Model. J. Biol. Chem. 2002, 277, 21480–21488. [Google Scholar] [CrossRef]
Dorin, J.R.; Dickinson, P.; Alton, E.W.F.W.; Smith, S.N.; Geddes, D.M.; Stevenson, B.J.; Kimber, W.L.; Fleming, S.; Clarke, A.R.; Hooper, M.L.; et al. Cystic Fibrosis in the Mouse by Targeted Insertional Mutagenesis. Nature 1992, 359, 211–215. [Google Scholar] [CrossRef]
Reynaert, I.; Van Der Schueren, B.; Degeest, G.; Manin, M.; Cuppens, H.; Scholte, B.; Cassiman, J.-J. Morphological Changes in the Vas Deferens and Expression of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) in Control, F508 and Knock-out CFTR Mice during Postnatal Life. Mol. Reprod. Dev. 2000, 55, 125–135. [Google Scholar] [CrossRef]
Orlowski, J. Heterologous Expression and Functional Properties of Amiloride High Affinity (NHE-1) and Low Affinity (NHE-3) Isoforms of the Rat Na/H Exchanger. J. Biol. Chem. 1993, 268, 16369–16377. [Google Scholar] [CrossRef]
Kurashima, K.; Yu, F.H.; Cabado, A.G.; Szabó, E.Z.; Grinstein, S.; Orlowski, J. Identification of Sites Required for Down-Regulation of Na+/H+ Exchanger NHE3 Activity by CAMP-Dependent Protein Kinase: Phosphorylation- Dependent and -Independent Mechanisms. J. Biol. Chem. 1997, 272, 28672–28679. [Google Scholar] [CrossRef] [PubMed]
Moe, O.W.; Amemiya, M.; Yamaji, Y. Activation of Protein Kinase A Acutely Inhibits and Phosphorylates Na/H Exchanger NHE-3. J. Clin. Invest. 1995, 96, 2187–2194. [Google Scholar] [CrossRef]
Yun, C.H.C.; Lamprecht, G.; Forster, D. V.; Sidor, A. NHE3 Kinase A Regulatory Protein E3KARP Binds the Epithelial Brush Border Na+/H+ Exchanger NHE3 and the Cytoskeletal Protein Ezrin. J. Biol. Chem. 1998, 273, 25856–25863. [Google Scholar] [CrossRef] [PubMed]
Donowitz, M.; Li, X. Regulatory Binding Partners and Complexes of NHE3. Physiol. Rev. 2007, 87, 825–872. [Google Scholar] [CrossRef]
Dong, Y.; Li, H.; Ilie, A.; Gao, Y.; Boucher, A.; Zhang, X.C.; Orlowski, J.; Zhao, Y. Structural Basis of Autoinhibition of the Human NHE3-CHP1 Complex. Sci. Adv. 2022, 8, 1–12. [Google Scholar] [CrossRef]
Wu, Y.N.; Chen, K.C.; Wu, C.C.; Lin, Y.H.; Chiang, H.S. SLC9A3 Affects Vas Deferens Development and Associates with Taiwanese Congenital Bilateral Absence of the Vas Deferens. Biomed Res. Int. 2019, 2019. [Google Scholar] [CrossRef]
Szászi, K.; Paulsen, A.; Szabó, E.Z.; Numata, M.; Grinstein, S.; Orlowski, J. Clathrin-Mediated Endocytosis and Recycling of the Neuron-Specific Na+/H+ Exchanger NHE5 Isoform: Regulation by Phosphatidylinositol 3′-Kinase and the Actin Cytoskeleton. J. Biol. Chem. 2002, 277, 42623–42632. [Google Scholar] [CrossRef]
Attaphitaya, S.; Park, K.; Melvin, J.E. Molecular Cloning and Functional Expression of a Rat Na+/H+ Exchanger (NHE5) Highly Expressed in Brain. J. Biol. Chem. 1999, 274, 4383–4388. [Google Scholar] [CrossRef]
Baird, N.R.; Orlowski, J.; Szabó, E.Z.; Zaun, H.C.; Schultheis, P.J.; Menon, A.G.; Shull, G.E. Molecular Cloning, Genomic Organization, and Functional Expression of Na+/H+ Exchanger Isoform 5 (NHE5) from Human Brain. J. Biol. Chem. 1999, 274, 4377–4382. [Google Scholar] [CrossRef]
Chen, X.; Wang, X.; Tang, L.; Wang, J.; Shen, C.; Liu, J.; Lu, S.; Zhang, H.; Kuang, Y.; Fei, J.; et al. Nhe5 Deficiency Enhances Learning and Memory via Upregulating Bdnf/TrkB Signaling in Mice. Am. J. Med. Genet. Part B Neuropsychiatr. Genet. 2017, 174, 828–838. [Google Scholar] [CrossRef]
Attaphitaya, S.; Nehrke, K.; Melvin, J.E. Acute Inhibition of Brain-Specific Na+/H+ Exchanger Isoform 5 by Protein Kinases A and C and Cell Shrinkage. Am. J. Physiol. - Cell Physiol. 2001, 281, 1146–1157. [Google Scholar] [CrossRef]
Jinadasa, T.; Szabó, E.Z.; Numata, M.; Orlowski, J. Activation of AMP-Activated Protein Kinase Regulates Hippocampal Neuronal PH by Recruiting Na+/H+ Exchanger NHE5 to the Cell Surface. J. Biol. Chem. 2014, 289, 20879–20897. [Google Scholar] [CrossRef] [PubMed]
Martin-Hidalgo, D.; de Llera, A.H.; Calle-Guisado, V.; Gonzalez-Fernandez, L.; Garcia-Marin, L.; Bragado, M.J. AMPK Function in Mammalian Spermatozoa. Int. J. Mol. Sci. 2018, 19. [Google Scholar] [CrossRef]
Gu, B.; Zhang, J.; Wu, Y.; Zhang, X.; Tan, Z.; Lin, Y.; Huang, X.; Chen, L.; Yao, K.; Zhang, M. Proteomic Analyses Reveal Common Promiscuous Patterns of Cell Surface Proteins on Human Embryonic Stem Cells and Sperms. PLoS One 2011, 6. [Google Scholar] [CrossRef]
Lawrence, S.P.; Bright, N.A.; Luzio, J.P.; Bowers, K. The Sodium/Proton Exchanger NHE8 Regulates Late Endosomal Morphology and Function. Mol. Biol. Cell 2010, 21, 3540–3551. [Google Scholar] [CrossRef]
Joseph, C.; Twombley, K.; Gattineni, J.; Zhang, Q.; Dwarakanath, V.; Baum, M. Acid Increases NHE8 Surface Expression and Activity in NRK Cells. Am. J. Physiol. - Ren. Physiol. 2012, 302, 495–503. [Google Scholar] [CrossRef]
Xu, H.; Chen, H.; Li, J.; Zhao, Y.; Ghishan, F.K. Disruption of NHE8 Expression Impairs Leydig Cell Function in the Testes. Am. J. Physiol. - Cell Physiol. 2015, 308, C330–C338. [Google Scholar] [CrossRef] [PubMed]
Xu, H.; Zhang, B.; Li, J.; Wang, C.; Chen, H.; Ghishan, F.K. Impaired Mucin Synthesis and Bicarbonate Secretion in the Colon of NHE8 Knockout Mice. Am. J. Physiol. - Gastrointest. Liver Physiol. 2012, 303, 335–343. [Google Scholar] [CrossRef]
Wiebe, S.A.; Plain, A.; Pan, W.; O’neill, D.; Braam, B.; Alexander, R.T. NHE8 Attenuates Ca2+ Influx into NRK Cells and the Proximal Tubule Epithelium. Am. J. Physiol. - Ren. Physiol. 2019, 317, F240–F253. [Google Scholar] [CrossRef] [PubMed]
Zhou, K.; Amiri, M.; Salari, A.; Yu, Y.; Xu, H.; Seidler, U.; Nikolovska, K. Functional Characterization of the Sodium/Hydrogen Exchanger 8 and Its Role in Proliferation of Colonic Epithelial Cells. Am. J. Physiol. Physiol. 2021, 321, C471–C488. [Google Scholar] [CrossRef]
Berger, T.K.; Fußhöller, D.M.; Goodwin, N.; Bönigk, W.; Müller, A.; Dokani Khesroshahi, N.; Brenker, C.; Wachten, D.; Krause, E.; Kaupp, U.B.; et al. Post-Translational Cleavage of Hv1 in Human Sperm Tunes PH- and Voltage-Dependent Gating. J. Physiol. 2017, 595, 1533–1546. [Google Scholar] [CrossRef]
López-González, I.; Torres-Rodríguez, P.; Sánchez-Carranza, O.; Solís-López, A.; Santi, C.M.; Darszon, A.; Treviño, C.L. Membrane Hyperpolarization during Human Sperm Capacitation. Mol. Hum. Reprod. 2014, 20, 619–629. [Google Scholar] [CrossRef] [PubMed]
Brown, S.G.; Publicover, S.J.; Mansell, S.A.; Lishko, P. V.; Williams, H.L.; Ramalingam, M.; Wilson, S.M.; Barratt, C.L.R.; Sutton, K.A.; Da Silva, S.M. Depolarization of Sperm Membrane Potential Is a Common Feature of Men with Subfertility and Is Associated with Low Fertilization Rate at IVF. Hum. Reprod. 2016, 31, 1147–1157. [Google Scholar] [CrossRef]
Calzada, L.; Tellez, J. Defective Function of Membrane Potential (Ψ) on Sperm of Infertile Men. Arch. Androl. 1997, 38, 151–155. [Google Scholar] [CrossRef]
Chávez, J.C.; de la Vega-Beltrán, J.L.; Escoffier, J.; Visconti, P.E.; Treviño, C.L.; Darszon, A.; Salkoff, L.; Santi, C.M. Ion Permeabilities in Mouse Sperm Reveal an External Trigger for SLO3-Dependent Hyperpolarization. PLoS One 2013, 8, 1–13. [Google Scholar] [CrossRef]
Geng, Y.; Ferreira, J.J.; Dzikunu, V.; Butler, A.; Lybaert, P.; Yuan, P.; Magleby, K.L.; Salkoff, L.; Santi, C.M. A Genetic Variant of the Sperm-Specific SLO3 K+ Channel Has Altered PH and Ca2+ Sensitivities. J. Biol. Chem. 2017, 292, 8978–8987. [Google Scholar] [CrossRef] [PubMed]
Sánchez-Carranza, O.; Torres-Rodríguez, P.; Darszon, A.; Treviño, C.L.; López-González, I. Pharmacology of HSlo3 Channels and Their Contribution in the Capacitation-Associated Hyperpolarization of Human Sperm. Biochem. Biophys. Res. Commun. 2015, 466, 554–559. [Google Scholar] [CrossRef] [PubMed]
Nomura, M.; Vacquier, V.D. Proteins Associated with Soluble Adenylyl Cyclase in Sea Urchin Sperm Flagella. Cell Motil. Cytoskeleton 2006, 63, 582–590. [Google Scholar] [CrossRef] [PubMed]
Miller, M.R.; Mannowetz, N.; Iavarone, A.T.; Safavi, R.; Gracheva, E.O.; Smith, J.F.; Hill, R.Z.; Bautista, D.M.; Kirichok, Y.; Lishko, P. V. Unconventional Endocannabinoid Signaling Governs Sperm Activation via the Sex Hormone Progesterone. Science (80-. ). 2016, 352, 555–559. [Google Scholar] [CrossRef]
Qi, H.; Moran, M.M.; Navarro, B.; Chong, J.A.; Krapivinsky, G.; Krapivinsky, L.; Kirichok, Y.; Ramsey, I.S.; Quill, T.A.; Clapham, D.E. All Four CatSper Ion Channel Proteins Are Required for Male Fertility and Sperm Cell Hyperactivated Motility. Proc. Natl. Acad. Sci. U. S. A. 2007, 104, 1219–1223. [Google Scholar] [CrossRef]
Lishko, P. V.; Botchkina, I.L.; Fedorenko, A.; Kirichok, Y. Acid Extrusion from Human Spermatozoa Is Mediated by Flagellar Voltage-Gated Proton Channel. Cell 2010, 140, 327–337. [Google Scholar] [CrossRef]
Miller, M.R.; Kenny, S.J.; Mannowetz, N.; Mansell, S.A.; Wojcik, M.; Mendoza, S.; Zucker, R.S.; Xu, K.; Lishko, P. V. Asymmetrically Positioned Flagellar Control Units Regulate Human Sperm Rotation. Cell Rep. 2018, 24, 2606–2613. [Google Scholar] [CrossRef]
Geragotelis, A.D.; Wood, M.L.; Göddeke, H.; Hong, L.; Webster, P.D.; Wong, E.K.; Freites, J.A.; Tombola, F.; Tobias, D.J. Voltage-Dependent Structural Models of the Human Hv1 Proton Channel from Long-Timescale Molecular Dynamics Simulations. Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 13490–13498. [Google Scholar] [CrossRef]
Miller, M.R.; Mansell, S.A.; Meyers, S.A.; Lishko, P. V. Flagellar Ion Channels of Sperm: Similarities and Differences between Species. Cell Calcium 2015, 58, 105–113. [Google Scholar] [CrossRef] [PubMed]
Ramsey, I.S.; Ruchti, E.; Kaczmarek, J.S.; Clapham, D.E. Hv1 Proton Channels Are Required for High-Level NADPH Oxidase-Dependent Superoxide Production during the Phagocyte Respiratory Burst. Proc. Natl. Acad. Sci. U. S. A. 2009, 106, 7642–7647. [Google Scholar] [CrossRef]
Zhao, R.; Dai, H.; Arias, R.J.; De Blas, G.A.; Orta, G.; Pavarotti, M.A.; Shen, R.; Perozo, E.; Mayorga, L.S.; Darszon, A.; et al. Direct Activation of the Proton Channel by Albumin Leads to Human Sperm Capacitation and Sustained Release of Inflammatory Mediators by Neutrophils. Nat. Commun. 2021, 12. [Google Scholar] [CrossRef]
Zhao, R.; Kennedy, K.; De Blas, G.A.; Orta, G.; Pavarotti, M.A.; Arias, R.J.; de la Vega-Beltrán, J.L.; Li, Q.; Dai, H.; Perozo, E.; et al. Role of Human Hv1 Channels in Sperm Capacitation and White Blood Cell Respiratory Burst Established by a Designed Peptide Inhibitor. Proc. Natl. Acad. Sci. U. S. A. 2018, 115, E11847–E11856. [Google Scholar] [CrossRef]
Florman, H.M.; Ducibella, T. CHAPTER 2 - Fertilization in Mammals. In; Neill, J.D.B.T.-K. and N.P. of R. (Third E., Ed.; Academic Press: St Louis, 2006; pp. 55–112. ISBN 978-0-12-515400-0. [Google Scholar]
Wagoner, K.; Sanchez, G.; Nguyen, A.N.; Enders, G.C.; Blanco, G. Different Expression and Activity of the A1 and A4 Isoforms of the Na,K-ATPase during Rat Male Germ Cell Ontogeny. Reproduction 2005, 130, 627–641. [Google Scholar] [CrossRef]
Sanchez, G.; Nguyen, A.N.T.; Timmerberg, B.; Tash, J.S.; Blanco, G. The Na,K-ATPase A4 Isoform from Humans Has Distinct Enzymatic Properties and Is Important for Sperm Motility. Mol. Hum. Reprod. 2006, 12, 565–576. [Google Scholar] [CrossRef] [PubMed]
Woo, A.L.; James, P.F.; Lingrel, J.B. Sperm Motility Is Dependent on a Unique Isoform of the Na,K-ATPase. J. Biol. Chem. 2000, 275, 20693–20699. [Google Scholar] [CrossRef]
Hlivko, J.T.; Chakraborty, S.; Hlivko, T.J.; Sengupta, A.; James, P.F. The Human Na,K-ATPase Alpha4 Isoform Is a Ouabain-Sensitive Alpha Isoform That Is Expressed in Sperm. Mol. Reprod. Dev. 2006, 73, 101–115. [Google Scholar] [CrossRef] [PubMed]
Lestari, S.W.; Miati, D.N.; Seoharso, P.; Sugiyanto, R.; Pujianto, D.A. Sperm Na+, K+-ATPase A4 and Plasma Membrane Ca2+-ATPase (PMCA) 4 Regulation in Asthenozoospermia. Syst. Biol. Reprod. Med. 2017, 63, 294–302. [Google Scholar] [CrossRef]
Jimenez, T.; McDermott, J.P.; Sánchez, G.; Blanco, G. Na, K-ATPase A4 Isoform Is Essential for Sperm Fertility. Proc. Natl. Acad. Sci. U. S. A. 2011, 108, 644–649. [Google Scholar] [CrossRef] [PubMed]
Jimenez, T.; Sánchez, G.; Blanco, G. Activity of the Na,K-ATPase A4 Isoform Is Regulated during Sperm Capacitation to Support Sperm Motility. J. Androl. 2012, 33, 1047–1057. [Google Scholar] [CrossRef] [PubMed]
Arcos-Hernández, C.; Suárez-Delgado, E.; Islas, L.D.; Romero, F.; López-González, I.; Ai, H. wang; Nishigaki, T. How to Study a Highly Toxic Protein to Bacteria: A Case of Voltage Sensor Domain of Mouse Sperm-Specific Sodium/Proton Exchanger. Protein Expr. Purif. 2023, 201. [Google Scholar]

Figure 1. Human SLC9 phylogenetic tree. Phylogenetic relations of human SLC9 proteins were calculated using Clustal Omega (https://www.ebi.ac.uk/Tools/msa/clustalo/), and the tree was generated using Interactive Tree of Life (https://itol.embl.de/) [41]. Protein sequence identifiers: SLC9A1, NP_003038.2; SLC9A2, NP_003039.2; SLC9A3, NP_004165.2; SLC9A4, NP_001011552.2; SLC9A5, NP_004585.1; SLC9A6, NP_001036002.1; SLC9A7, NP_001244220.1; SLC9A8, NP_001247420.1; SLC9A9, NP_775924.1; SLC9B1, NP_631912.3; SLC9B2, NP_849155.2; SLC9C1, NP_001307460.1; SLC9C2, NP_848622.2. The SLC9A subfamily is highlighted in orange and is further divided into SLC9A1-5 because of their established plasma membrane localization and then SLC9A6-9 which localize intracellularly (note NHE3, NHE5, and NHE8 has reported both intracellular and plasma membrane localizations). The SLC9B subfamily is highlighted in green while the SLC9C subfamily is highlighted in gray. Reprinted/adapted from [42].

Figure 2. NHE structural features. A) Topology of human NHE1. The structure of human NHE1 was solved and found to contain 13 transmembrane domains which comprise a conserved NHE domain [47]. The NHE1-9 isoforms are all predicted to contain an NHE domain within their transmembrane domains as well as short N-termini and long intracellular C-termini of varying lengths and functions. NHE1 is known to have multiple regulatory domains in the intracellular C-terminus which control different aspects of pH sensing as well as the cell cycle. B) Topology of bison NHA2. The structure of bison NHA2 was solved and found to possess 14 transmembrane domains. Both the NHA1 and NHA2 human isoforms are also predicted to contain an NHE domain within their 14 transmembrane domains as well as an intracellular N-terminus and a short C-terminus. C) Predicted topology of human NHE10. Both human NHE10 and NHE11 are predicted to contain an NHE domain within the first 13 transmembrane domains, followed by 4 transmembrane domains comprising a voltage sensing domain (VSD) (orange), followed by an intracellular cyclic nucleotide binding domain (CNBD) (green). Topology cartoon created with Biorender.com.

Figure 3. RNA sequencing data of SLC9 genes expressed in testis/sperm. A and B) Digital PCR (heatmap) of SLC9 genes expressed in testis/sperm displaying relative expression of these genes across different testis cell types in A) human and B) mice. DYNC1I2 is included as a loading control in both the human and mouse heatmaps. SSEA-4 is a marker for repopulating human spermatogonial stem cells [49], and Kit is a marker for differentiating spermatogonia [50,51]. Spermatogonia exhibiting high ID4 expression are hallmarks of renewing spermatogonial stem cells, whereas lower ID4 expression is associated with spermatogonia that are in transition to the progenitor state [52]. Note that SLC9C2 is annotated as a pseudogene in mice and therefore there is no RNA-seq data for this gene in mice. This data is taken and the figures generated from the Mammalian Reproductive Genetics Database V2 (https://orit.research.bcm.edu/MRGDv2) [53]. Note that only SLC9 genes for which there is published data of their protein expression in testis/sperm from the literature is included in this figure.

Figure 4. Subcellular NHE localization in rodent and human spermatozoa. NHE1 and NHE5 are known to localize to the midpiece in rat sperm [48], potentially playing a role in energy homeostasis or simply in basal pH regulation. NHA1 has been reported to localize to the principal piece in human and both the principal piece and midpiece in mouse sperm and NHA2 has been reported to localize to the principal piece in mouse sperm [10,11]. NHE10 has been reported to localize to the principal piece in mouse sperm [8]. In different publications, human NHE10 has been reported to localize to either the entire flagellum [54] or just the principal piece [12]. Localization of NHEs to the principal piece may help support sperm motility because intracellular pH regulation of the principal piece greatly influences sperm motility. NHE11 has recently been reported to localize specifically to the sperm head, likely the plasma membrane overlying the acrosome, in both rat and human sperm [42]. The exact role of NHE11 in the sperm head is unclear but could potentially regulate the acrosome reaction or sperm/egg fusion events. Note that neither NHE3 nor NHE8 proteins have yet to be demonstrated to be expressed in mature sperm cells. Sperm cartoon created with Biorender.com.

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

Copyright: This open access article is published under a Creative Commons CC BY 4.0 license, which permit the free download, distribution, and reuse, provided that the author and preprint are cited in any reuse.

MDPI Initiatives

Important Links

Choose an area of interest and we will send you notifications of new preprints at your preferred frequency.

Disclaimer