Figures
Abstract
Acid-sensing ion channels (ASICs) are Na+ channels activated by changes in pH within the peripheral and central nervous systems. Several different isoforms of ASICs combine to form trimeric channels, and their properties are determined by their subunit composition. ASIC2 subunits are widely expressed throughout the brain, where they heteromultimerize with their partnering subunit, ASIC1a. However, ASIC2 contributes little to the pH sensitivity of the channels, and so its function is not well understood. We found that ASIC2 increased cell surface levels of the channel when it is coexpressed with ASIC1a, and genetic deletion of ASIC2 reduced acid-evoked current amplitude in mouse hippocampal neurons. Additionally, ASIC2a interacted with the neuronal synaptic scaffolding protein PSD-95, and PSD-95 reduced cell surface expression and current amplitude in ASICs that contain ASIC2a. Overexpression of PSD-95 also reduced acid-evoked current amplitude in hippocampal neurons. This result was dependent upon ASIC2 since the effect of PSD-95 was abolished in ASIC2−/− neurons. These results lend support to an emerging role of ASIC2 in the targeting of ASICs to surface membranes, and allows for interaction with PSD-95 to regulate these processes.
Citation: Harding AMS, Kusama N, Hattori T, Gautam M, Benson CJ (2014) ASIC2 Subunits Facilitate Expression at the Cell Surface and Confer Regulation by PSD-95. PLoS ONE 9(4): e93797. https://doi.org/10.1371/journal.pone.0093797
Editor: Michael B. Butterworth, University of Pittsburgh, School of Medicine, United States of America
Received: February 4, 2014; Accepted: March 6, 2014; Published: April 3, 2014
Copyright: © 2014 Harding et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: National Institute of Health, National Heart, Lung, and Blood Institute (R01 HL076419), and Department of Veterans Affairs (Merit Award BX000776). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
ASICs are H+-gated Na+-conducting ion channels predominantly expressed in the nervous systems of chordates. In mammals, 4 genes (ASIC1-4) encode for at least 6 different ASIC subunits [1]. In rodents, ASIC1 and ASIC2 have alternative splice forms (ASIC1a and -1b; -2a and -2b, respectively), which differ in the intracellular N-termini and first transmembrane domains. ASICs are assembled as either homo- or hetero-trimeric complexes, and each combination of subunits forms channels with unique biophysical properties [2], [3], [4]. ASIC1a is the major determinant of pH-activated currents in central nervous system (CNS) neurons [5], [6], [7]. Expressed at the soma and in dendrites, including post-synaptic sites, ASIC1a is positioned to sense local pH changes within the brain [6], [8]. ASIC1a plays a role in some forms of learning and memory, and it seems particularly important for innate fear responses and acquired fear-conditioned behaviors [6], [9], [10], [11]. In addition, pharmacological or genetic perturbation of ASIC1 alters outcomes in mouse models of stroke and seizures – pathological conditions associated with tissue acidosis [12], [13]. In contrast to ASIC1a, ASIC3 is predominantly expressed in peripheral sensory neurons, where it contributes to pain sensation, including that from the heart and skeletal muscle [14], [15], [16], [17], [18]. Similarly, ASIC1b is primarily expressed in the periphery and participates in pain [19], [20]. ASIC4 does not contribute to H+-gated currents, and its function in mammals is largely unknown [21], [22].
ASIC2 subunits are widely expressed in both the central and peripheral nervous systems [23], [24], [25]. However the function of ASIC2 is less well understood. The splice variant ASIC2a forms H+-gated homomeric channels when expressed alone, but ASIC2a homomers are far less pH sensitive than other ASICs – requiring pH levels below 5.0 to be activated. Moreover, ASIC2a homomeric-like currents have not been described in wildtype native neurons. ASIC2b does not form functionally active channels when expressed alone. On the other hand, ASIC2 subunits can heteromultimerize with other subunits to generate channels with unique functional properties [3], [4], [26], [27]. For example, we recently found that ASIC2 and -3 function as heteromultimeric channels (ASIC2/3) in mouse sensory neurons in the dorsal root ganglion (DRG) that innervate the heart [28]. In contrast, we found that ASIC1/2/3 heteromers predominate in skeletal muscle sensory neurons [29]. Several studies investigating the role of ASIC2 in the periphery suggest that it might play a role in mechanosensation [30], [31], similar to the function of the related degenerin (DEG) channels in Caenorhabditis elegans [32], although the role of ASICs as mechano-transducers is uncertain [33], [34], [35]. In the CNS, ASIC2 subunits primarily form heteromultimers with ASIC1a. Electrophysiological studies of hippocampal, cortical, and spinal cord neurons identified acid-evoked currents that are the result of a combination of ASIC1a homomers, ASIC1a/2a heteromers, and ASIC1a/2b heteromers [5], [7], [36], [37]. Compared to ASIC1a homomers, ASIC1a/2a heteromers are slightly less pH sensitive and have faster kinetics of desensitization [3], [4]. When ASIC2b heteromultimerizes with ASIC1a in CNS neurons, ASIC2b imparts altered pharmacology and slight shifts in ion selectivity [37].
Despite the relatively subtle effects of ASIC2 subunits on the biophysical properties, recent studies demonstrate that ASIC2 is important for normal brain function. Genetic deletion of ASIC2 generates neurological behavior deficits that mimic those seen in ASIC1a −/− mice [38]. Moreover, human genetic linkage studies have associated the ASIC2 locus with autism, panic disorder, and lithium responsiveness in bipolar disorder [39], [40], [41]. Recent work has begun to elucidate the underlying mechanisms. ASIC2 facilitates ASIC channel localization to synapses on neuronal dendritic spines – sites of excitatory synapses. This effect, in part, is dependent upon ASIC2 interaction with the synaptic scaffolding protein, postsynaptic density-95 (PSD-95) [42]. Here, we explored the role of ASIC2 subunits on the expression of ASIC channels at the cell surface, and tested if PSD-95 can alter the functional expression of ASIC2 containing channels in both heterologous cells and hippocampal neurons.
Materials and Methods
Heterologous Expression of cDNA in CHO Cells
Mouse ASIC1a, mouse ASIC2a, and rat PSD-95 in pMT3 vectors were cloned as previously described [42], [43]. Human ASIC2b was kindly provided by Dr. Michael Welsh. HA-ASIC1a, HA-ASIC2a, and ASIC2aGAA (replacement of the C-terminal 3 aa with Gly-Ala-Ala) were described earlier [42], [44]. DsRed (Express-C1) was purchased from Clontech, and green fluorescent protein (GFP; pGreen Lantern) was from Life Technologies. Chinese Hamster Ovarian (CHO) cells (ATCC, Manassas, Virginia) were cultured at 37°C, 5% CO2 in F12 nutrient medium (Gibco, Carlsbad, CA) supplemented with 10% fetal bovine serum and 1% penicillin/streptomycin. For electrophysiological studies, cells plated in 35 mm dishes at ∼10% confluence were transfected with ASIC cDNAs (0.18 μg/1.5 ml), PSD-95 or DsRed as control (1.82 μg/1.5 ml), and GFP (0.33 μg/1.5 ml) to facilitate detection of expressing cells by epifluorescence using lipid transfection reagent TransFast (Promega, Madison, WI) according to manufacturer’s recommendations. Coexpressed ASIC cDNAs were transfected at equal concentration for a total of 1.82 μg/1.5 ml. Cells were studied 2 days after transfection. Cells used for biochemistry were transfected with 7.5 μg of HA-ASIC1a or HA-ASIC2a and 7.5 μg of ASIC2a, ASIC2b constructs, or DsRed cDNA using Lipofectamine 2000 (Gibco, Carlsbad, CA) in 100 mm dishes. For experiments testing the effect of PSD-95 we transfected 7.5 μg of HA-ASIC2a or HA-ASIC1a and ASIC2a (total 7.5 μg), and 7.5 μg PSD-95 or dsRed cDNA. Our transfection protocol for electrophysiological studies has low efficiency, but transfected cells are easy to patch clamp and have large currents, whereas our transfection protocol for biochemistry is highly efficient to generate a large quantity of protein.
Antibodies
The following antibodies were used: anti-HA-Peroxidase, High Affinity antibody (clone 3F10) (Roche Applied Biosciences, Indianapolis, IN), and anti-PSD-95 (6G6) (Santa Cruz Biotechnology, Santa Cruz, CA).
Surface Biotinylation and NeutrAvidin Pulldown
48 hours after transfection, cells were incubated at 4°C for 5 minutes, followed by three washes at 4°C with PBS+ (1 mM PBS, pH 7.4; 1 mM MgCl2; 1 mM CaCl2), then incubated with 0.5 mg/ml sulfo-N-hydroxysuccinimide-biotin (Thermo Scientific Pierce, Rockford, IL) at 4°C for 30 minutes. Unbound biotin was quenched with 100 mM glycine in PBS+for 20 minutes at 4°C. The cells were lysed at 4°C for 20 min using 1% Nonidet P-40/63 mM EDTA/58.3 mM Tris-HCl pH 8/9.6 mM sodium deoxycholate, plus protease inhibitors (Sigma). The supernatant was pre-cleared with 50 μl of washed Protein A-Sepharose beads (Thermo Scientific Pierce, Rockford, IL) and then centrifuged at 16,100×g for 10 minutes at 4°C to remove insoluble material. 800 μg of lysate was tumbled with 30 μl NeutrAvidin-agarose beads (Thermo Scientific Pierce, Rockford, IL) for 24 hours at 4°C. After three washes, biotinylated proteins were eluted using SDS sample buffer (4% SDS; 100 mM DTT; 20% glycerol; 100 mM Tris·HCl, pH 6.8), separated by SDS/PAGE and then immunoblotted.
Immunoprecipitation
Cells were washed at 4°C three times with PBS+ (1 mM PBS, pH 7.4; 1 mM MgCl2; 1 mM CaCl2), and then incubated for 20 min on a rocker at 4°C in 1 ml of lysis buffer [1% TX-100/50 mM Tris-HCl, pH 7.5/150 mM NaCl/1 Complete Mini protease inhibitor tablet/25–50 ml (Roche Applied Biosciences, Indianapolis, IN)]. Following centrifugation (16,100×g, 4°C, 10 min), the supernatant was pre-cleared with 50 μl of washed Protein A-Sepharose beads. Samples were tumbled with 1 μg of PSD95 antibody with 50 μl of Protein A-Sepharose beads. The immunoprecipitates were collected by centrifugation, washed three times with lysis buffer, and then resolved by SDS-PAGE.
Immunoblotting
Samples were separated by SDS-PAGE on a 7.5% (w/v) gel and transferred to a Protran nitrocellulose membrane (Whatman, Dassel, Germany). The membrane was blocked in 5% bovine serum albumin (BSA) in TBS-Tween (0.05% (w/v) Tween-20 in 10 mM Tris, 100 mM NaCl, pH 7.5), and then incubated with the primary antibody (anti-HA-HRP, 1∶750) in 1% BSA/TBS-Tween. Membranes were developed using the Amersham ECL Plus Western Blotting Detection System (GE Healthcare, Buckinghamshire, UK). Bands were quantified with ImageJ.
Electrophysiology
Whole-cell patch-clamp recordings (at −70 mV) from CHO cells and mouse hippocampal neurons were performed at room temperature with an Axopatch 200B amplifier (Axon Instruments, Foster City, CA) and were acquired and analyzed with PULSE/PULSEFIT 8.70 (HEKA Electronics, Lambrecht, Germany) and IGOR Pro 6.01 (WaveMetrics, Lake Oswego, OR) software or pCLAMP 8.2 (Axon Instruments). Recordings were filtered at 5 kHz and sampled at 2 or 0.2 kHz. Capacitive currents were compensated for and recorded for normalization of peak current amplitudes (reported as current densities). Micropipettes (2–4 MΩ) were filled with internal solution (mM): 100 KCl, 10 EGTA, 40 HEPES, 5 MgCl2, 2 Na2ATP, and 0.3 Na3GTP, pH 7.4 with KOH. External solution contained (mM): 120 NaCl, 5 KCl, 1 MgCl2, 2 CaCl2, 10 HEPES, 10 MES, pH adjusted with tetramethylammonium hydroxide, and osmolarity adjusted with tetramethylammonium chloride. Extracellular solutions were changed within 20 msec by using a computer-driven solenoid valve system [45]. Control solution (pH 8) flowed on cells for 30 s between acidic pH applications to allow for recovery from desensitization. Kinetics of desensitization was fit to single exponential equations and time constants (τ) reported. pH-dependent activation curves were fit to the Hill equation with IGOR Pro 6.01.
Hippocampal Neuron Culture and Transfection
Primary hippocampal neuron cultures were prepared from postnatal day 0–2 mouse pups. Pups were placed on ice and then euthanized by rapid decapitation to minimize suffering. Hippocampi were rapidly dissected and digested for 2 min with 0.06% Trypsin-EDTA in Hank’s balanced salt solution without Mg2+ or Ca2+ (HBSS−/−; Gibco) plus glucose (6 mg/ml). Hippocampi were then washed with 10 ml followed by trituration in 2 ml HBSS−/− plus glucose. Following a 1-minute incubation, the upper portion of the suspension was transferred to a new tube (leaving behind ∼500 μl debris) and cells were pelleted by centrifugation (1000 rpm, 1 min). The pellet was then resuspended with plating medium [Neurobasal+B27+ Glutamax (Gibco) +5% horse serum], plated onto poly-lysine and laminin coated coverslips at a density of 4–6×105 cells/35 mm dish, and maintained in a 37°C humidified 5% CO2 incubator. Medium was changed 3–4 hr later to culture medium (Neurobasal+B27+ Glutamax) and then changed every 3–4 days. Calcium phosphate mediated transfection was performed 5–6 days after plating. Before transfection, conditioned medium was saved and cells were washed with sequentially with HBSS with Mg2+ or Ca2+ (HBSS+/+; Gibco) and fresh culture medium. For each 35 mm dish, 7.5 μg of total DNA was diluted to a final volume of 20 μl with sterile ddH2O and mixed with 42.5 μl of 250 mM CaCl2. The DNA/Ca2+ mix was added dropwise to an equal volume of 2×HBS (mM: 50 HEPES, 280 NaCl, 1.5 Na2HPO4, pH 7.0) and mixed by pipetting. Precipitates were allowed to form by incubating at room temperature for 20–30 min and then the suspension was added dropwise to dishes. 1–2 hr after transfection, cultures were washed once with HBSS+/+ and twice with culture medium. Conditioned medium was then added back to cultures. Neurons were returned to the incubator and electrophysiological studies were performed 1–2 days later.
Ethics Statement
All animal procedures and care were followed in strict accordance with the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health and approved by the Institutional Animal Care and Use Committee of the University of Iowa. For preparation of primary hippocampal neuron cultures, postnatal day 0–2 mouse pups were placed on ice and then euthanized by rapid decapitation to minimize suffering.
Results
ASIC2a Increases ASIC1a Cell Surface Expression and Current Amplitude
We tested the functional effects of ASIC2a on ASIC currents when co-expressed with ASIC1a. For comparison, we also studied ASIC1a and ASIC2a homomers. When exposed to an acidic pH solution, CHO cells expressing either ASIC1a or ASIC2a subunits generated rapidly activating and desensitizing currents (Fig. 1A). However the properties of these currents differed markedly. As per previous reports, ASIC1a homomeric channels were activated by relatively modest pH changes (pH50 = 6.7), whereas ASIC2a homomers required much lower pH values for activation (pH50 = 4.0) (Fig. 1B and [3]). Coexpression of ASIC1a and -2a generated currents with properties consistent with heteromeric channels. The pH sensitivity of activation for the heteromeric channel was between that of the homomeric channels (pH50 = 5.4; Fig. 1B). In addition, pH 5-evoked current from ASIC1a/2a heteromers desensitized at a faster rate than ASIC1a homomeric channels (Fig. 1C). Interestingly, acid-evoked currents recorded from CHO cells transfected with both ASIC1a and -2a were consistently larger than those from cells expressing ASIC1a alone, even though the total concentration of transfected ASIC cDNA was equal (Fig. 2A and D). Of note, the amplitude of ASIC2a homomeric pH 4-evoked current is not reflective of the total number of channels at the cell surface because even at pH 3.5, the dose-response curve for activation of ASIC2a homomers has not reached a plateau (see Fig. 1B). On the other hand, pH 4 maximally activates ASIC1a and ASIC1a/2a channels.
A, Representative acid-evoked currents generated by pH 4 application to CHO cells transfected with the indicated ASIC subunits. Coexpressed ASICs were expressed at half the normal amount to keep total ASIC cDNA constant. The bar above each current trace represents the time that the perfusing solution was rapidly changed from pH 7.4 to 4. B, pH-dose response curves for activation of cells expressing ASIC1a, ASIC2a, or coexpressing ASIC1a and ASIC2a. Data were acquired by stepping from pH 7.4 to the indicated test solution, and are normalized to the maximal currents (n ≥6). Lines are fits of the Hill equation. C, Superimposed pH 5-evoked currents from cells expressing ASIC1a or coexpressed ASIC1a and -2a (vertical scale bar: 3.66 nA ASIC1a and 5 nA coexpressed ASIC1a and -2a). To the right are the mean time constants (τ) of desensitization as measured from single exponential fits to the falling phase of currents evoked by pH 5 (n ≥8; *P<0.01). D, Mean current densities evoked by pH 4 in cells expressing the indicated ASIC subunits (n ≥6; *P<0.01 compared to ASIC1a expressed alone).
A, C, and E, Immunoblots (IB) (anti-HA) of biotinylated (surface) and total ASIC1a or -2a in CHO cells transfected with the indicated ASIC subunits (7.5 μg). The immunoblotted ASIC subunit was epitope-tagged with HA to allow detection. DsRed cDNA was added to keep total cDNA constant. Lanes for surface and total protein were from the same gel and film exposures respectively, but were rearranged for clarity. B, D, and F, Indicated ASIC surface expression is quantitated and normalized to the total amount of ASIC in the cell lysate for data from A, C, and E, respectively (n ≥5; *P<0.05; n.s. indicates no significant difference).
The increase in current amplitudes when ASIC2a is coexpressed with ASIC1a could be due to an increase in conductance and/or an increase in channel expression at the cell surface. To test the later, we labeled ASIC1a at the cell surface with sulfo-NHS-biotin to allow isolation with Neutravidin. Compared to ASIC1a expressed alone, ASIC1a surface levels were increased when it was coexpressed with ASIC2a (Fig. 2A). When normalized to the total amount of ASIC1a in the cell lysate, coexpression of ASIC2a significantly increased the relative ASIC1a surface/total protein expression (Fig. 2B). We suspect that the greater increase in surface expression (∼7-fold), compared to the ∼2.5-fold increase in current (Fig. 1D), reflects a difference in the transfection protocols (see methods). We also tested the effect of the ASIC2 splice variant, ASIC2b, on ASIC1a cell surface expression. Like ASIC2a, -2b also increased the relative amount of ASIC1a at the cell surface (Fig. 2C and D). Conversely, ASIC1a did not increase the cell surface expression of ASIC2a (Fig. 2E and F). These results suggest that ASIC2 subunits facilitate expression of ASIC1a at the cell surface, and increase the number of functional channels available for activation.
Next we tested the effect of ASIC2 subunits on ASIC currents in cultured hippocampal neurons, where most ASIC2 subunits heteromultimerize with ASIC1a subunits to form H+-gated channels [5], [37]. pH 5 applications generated ASIC-like currents in most hippocampal neurons, and this was also true for neurons from mice that had targeted deletion of the ASIC2 gene (Fig. 3A). As previously reported [5], loss of ASIC2 generated currents that had significantly increased pH sensitivity as measured by the ratio of pH 6.8-evoked current to pH 5-evoked current amplitudes (Fig. 3B), and significantly slower desensitization kinetics (Fig. 3C and D). The properties of acid-evoked currents in ASIC2−/− neurons are consistent with those of ASIC1a homomeric channels [3], [5]. Importantly, and in agreement with our data in heterologous cells, ASIC currents in ASIC2−/− neurons were of significantly smaller amplitude than those from wildtype neurons (Fig. 3A and E). In summary, these data suggest that heteromultimerization of ASIC2 subunits with ASIC1a facilitate channel expression at the cell surface and increases acid-evoked current amplitudes.
A, Representative pH 5-evoked currents from wildtype and ASIC2−/− cultured mouse hippocampal neurons. B, The ratio of pH 6.8-evoked to pH 5-evoked current amplitudes as a measure of pH sensitivity (n ≥9; *P<0.01). C, Superimposed pH 5-evoked currents from hippocampal neurons of the indicated genotypes (vertical scale bar: 1 nA wildtype and 0.58 nA ASIC2−/−). D, Mean time constants (τ) of desensitization (n ≥11; *P<0.05). E, Mean current amplitude density evoked by pH 5 (n ≥11; *P<0.01).
PSD-95 Reduces ASIC2a Cell Surface Expression and ASIC2a Acid-evoked Currents
ASIC2a can also interact with other proteins to modulate ASIC function and cell surface expression. We previously found that PSD-95 interacts specifically with ASIC2 in CNS neurons and targets ASIC channels to dendritic spines, the primary site of excitatory synapses [42]. Here we tested if PSD-95 alters the functional properties of ASIC2a. First we confirmed that ASIC2a interacts with PSD-95 when coexpressed in CHO cells. As shown in other cells [42], ASIC2a coimmunoprecipitated with PSD-95 (Fig. 4A). Next we tested if PSD-95 might alter ASIC2a cell surface expression. Figure 4B shows that PSD-95 decreased the amount of ASIC2a expressed at the cell surface without changing the total ASIC2a expressed in the cell (Fig. 4B), resulting in a significant decrease in relative ASIC2a cell surface/total protein expression (Fig. 4C).
A–C, CHO cells were transfected with HA-ASIC2a and/or PSD-95, with DsRed added to keep total cDNA constant. A, Coimmunoprecipitation of ASIC2a with PSD-95. In the top panels, cell lysates were immunoprecipitated (IP) with anti-PSD-95 antibody, and then immunoblotted (IB) for ASIC2a (anti-HA). The bottom panels shows immunoblots of cell lysates. B, Immunoblot (anti-HA) of biotinylated (surface) and total ASIC2a. Lanes for surface and total protein in A and B were from the same gel and film exposure respectively, but were arranged for clarity. C, Quantification of relative ASIC2a surface expression with and without coexpressed PSD-95 (n = 9; *P<0.05).
We then tested if PSD-95 might modulate ASIC2a acid-evoked currents. As predicted from the surface expression data, coexpressing PSD-95 significantly reduced ASIC2a current amplitude (Fig. 5A and B). While PSD-95 reduced ASIC2a expression at the cell surface and decreased ASIC2a current amplitude, it did not significantly alter its biophysical properties including the rate of desensitization (Fig. 5C), pH sensitivity of activation (Fig. 5D), or recovery from desensitization (Fig. 5E). Thus, PSD-95 regulates ASIC2a by reducing its expression at the cell surface, and not by altering the biophysical properties of the channel. To test if this effect was dependent upon the PDZ-binding motif of ASIC2a, we mutated the three C-terminal amino acids of ASIC2a (Ile-Ala-Cys) to Gly-Ala-Ala (ASIC2aGAA). While ASIC2aGAA generated acid-evoked currents with similar amplitudes as wildtype ASIC2a, mutation of the PDZ-binding motif abolished its capacity to be regulated by PSD-95 (Fig. 5A and B).
A, Representative pH 3.5-evoked currents in CHO cells coexpressing wild-type ASIC2a or ASIC2aGAA with either dsRed as a control or PSD-95 at 1∶10 cDNA ratios. B, Mean current density of currents evoked by pH 3.5 for above cells (n ≥12; *P<0.01 compared to ASIC2a without PSD-95). C, Mean time constants (τ) of desensitization of pH 3.5-evoked currents from ASIC2a in the presence and absence of PSD-95 (n ≥28). D, pH-dose response curves for activation of cells expressing ASIC2a and PSD-95 (pH50 = 3.9; n ≥12). Currents were normalized to those evoked by pH 3.5 for the dose-response data. Line is fit of Hill equation. Dashed line is fit of ASIC2a data from Fig. 1B. E, The mean time to recovery from desensitization. Data was collected by applying a prolonged 20 sec pulse of pH 4 to the cells to allow current to completely desensitize. pH 7.4 was then applied for the indicated times before applying a second pH 4 pulse. Recovery is the percentage of current evoked by the second pulse compared to the first. Line is fit of single exponential and is superimposed for the two groups (τ = 0.57 sec for each group; n ≥17).
PSD-95 Alters ASIC1a Cell Surface Expression and Current Amplitudes when Coexpressed with ASIC2a
Previous work demonstrated that PSD-95 does not interact with ASIC1a and does not alter ASIC1a homomeric channel function [42], [46]. Since coexpression ASIC1a and ASIC2a predominantly results in heteromeric channels composed of both subunits (Fig. 1), we asked if PSD-95 might modulate ASIC1a if it was coexpressed with ASIC2 subunits. Figures 6A and B demonstrate that coexpression of PSD-95 with ASIC1a and -2a generated currents with smaller amplitudes compared to currents generated by ASICs expressed alone. Consistent with a reduction in current amplitudes, coexpression of PSD-95 along with ASIC2a, reduced the relative amount of ASIC1a at the cell surface (Fig. 6C and D).
A, Representative pH 5-evoked currents in CHO cells coexpressing ASIC1a and ASIC2a, with either dsRed as a control or PSD-95 at 1∶10 cDNA ratios. B, Mean current density of currents evoked by pH 5 for above groups of cells (n ≥7; *P<0.01 compared to without PSD-95). C, Immunoblot (anti-HA) of biotinylated (surface) and total ASIC1a when coexpressed in CHO cells with ASIC2a, with and without PSD-95. Lanes for surface and total protein in A were from the same gel and film exposure respectively, but were arranged for clarity. D, Quantification of mean relative surface to total ASIC1a (n ≥5, *P<0.05).
PSD-95 Decreases ASIC1a/2 Acid-evoked Currents in Hippocampal Neurons
Our data in heterologous cells demonstrated that ASIC2a, when it is a component of a heteromeric ASIC channel, imparts the capacity to be modulated by PSD-95. In CNS neurons, most ASIC2 subunits heteromultimerize with ASIC1a subunits to form H+-gated channels [5], [6]. To test the effects of PSD-95 on native channels, we overexpressed PSD-95 in cultured hippocampal neurons, and studied their acid-evoked currents. Figures 7A and B show that overexpression of PSD-95 significantly reduced the amplitude of pH 5.0-activated currents, whereas expression of GFP as a control had no effect. Although the currents were smaller, PSD-95 did not alter the pH sensitivity (as measured by the pH 6.8 to pH 5.0 current amplitude ratio; 0.185±0.045 for the GFP and 0.150±0.026 for PSD-95 groups). Also, the kinetics of desensitization of pH 5-evoked currents (τ = 0.72±0.05 s untransfected, 0.72±0.04 s GFP, 0.74±0.05 s PSD-95; n ≥12), and recovery from desensitization (% recovery at 1 s = 0.29±0.09 GFP, 0.22±0.04 PSD-95; n ≥7) were unchanged by PSD-95 overexpression. Based on our data to this point, we hypothesized that PSD-95 would have no effect in hippocampal neurons that lacked ASIC2 subunits. Indeed, overexpression of PSD-95 in ASIC2−/− neurons had no effect on acid-evoked currents (Fig. 7A and B). Thus, PSD-95 inhibition of ASIC current in hippocampal neurons was dependent on ASIC2.
A, Representative acid-evoked currents from wildtype or ASIC2−/− cultured mouse hippocampal neurons transfected with either GFP alone (GFP), or GFP and PSD-95 (PSD-95). B, Mean current densities evoked by pH 5.0 in the indicated groups of hippocampal neurons (n ≥10; *P<0.01 compared to both wildtype untransfected and GFP groups).
Discussion
Although ASIC2 was the first ASIC to be cloned almost two decades ago [24], its function has remained rather elusive. ASIC2a homomeric channels require very low pH values for activation (pH50 = 4.0 in this study), which is probably below the range achieved in vivo during physiological and even pathological conditions. ASIC2b does not form homomeric acid-gated channels. Moreover, when ASIC2a heteromultimerizes with other ASIC subunits, it generally reduces channel pH sensitivity, and when ASIC2b heteromultimerizes with other subunits, the pH sensitivity of activation is unaltered. Thus, ASIC2 subunits themselves probably do not serve as pH sensors. And yet, recently published data showed that targeted deletion of ASIC2 produced behavioral phenotypes that were remarkably similar to those seen in ASIC1a −/− mice [38]. Loss of either ASIC1a or ASIC2 similarly diminished unconditioned fear responses to predatory odor or CO2, and both genotypes showed similarly reduced conditioned fear behavior. In addition, ASIC1a and ASIC2 null mice demonstrated less depressive-like activity in a forced swim assay. On the whole, deletion of either ASIC1a or ASIC2 generated equal and maximal behavioral deficits, as mice that had combined loss of ASIC1a and ASIC2 did not display a greater phenotype than deletion of the individual genes.
These results raise the question: how does loss of ASIC2 generate behavioral phenotypes that mimic the loss of ASIC1a, when ASIC2 subunits contribute relatively little to the pH sensitivity of CNS neurons? Our results here lend insight. In heterologous cells, expression of ASIC2 subunits increased the surface expression of ASIC1a and increased acid-evoked current amplitude. In cultured hippocampal neurons, disruption of ASIC2 reduced current amplitude. Thus, when ASIC2 subunits heteromultimerize with ASIC1a, more channel protein is expressed at the cell surface, which can increase neuronal responses when exposed to local acidosis. However, it should be noted that a previous study did not show a difference in acid-evoked current amplitudes recorded from ASIC2−/− hippocampal neurons when compared to wildtype [5]. The reason for this difference is unclear. Consistent with our data here, ASIC2 facilitated the localization of ASICs to dendritic spines in brain slices of the hippocampus, and enriched ASIC expression in brain synaptosomal membrane fractions. Moreover, deletion of ASIC2 reduced acid-evoked intracellular Ca2+ elevations in dendritic spines [42]. These findings suggest an important role of ASIC2 subunits in the trafficking and localization of ASIC channels to synapses and perhaps extra-synaptic membrane sites where they can be activated by local changes in pH.
While our data support a role for ASIC2 in the subcellular localization of ASIC channels, changes in the biophysical channel properties conferred by ASIC2 subunits might also be important. For example, the faster kinetics of desensitization, and in particular the faster recovery from desensitization of ASIC1a/2a heteromers compared to ASIC1a homomers, might be important for repeated activation of ASICs under fluctuating pH conditions. The importance of desensitization kinetics for channel function is illustrated by the association of an inheritable form of epilepsy with mutant nicotinic acetylcholine receptors that display faster desensitization and slower recovery from desensitization [47].
How do ASIC2 subunits facilitate subcellular localization of ASIC channels? Our studies demonstrating a functional interaction between ASIC2 and the neuronal scaffolding protein PSD-95 provide clues. ASIC subunits differ most in their intracellular N- and C-termini. Within these cytoplasmic regions, several subunit specific protein interaction motifs have been identified that regulate ASIC trafficking and function. The C-terminal residues of ASIC1, -2, and -3 each contain distinctive PDZ-binding motifs that allow for interaction with different cytosolic PDZ domain-containing proteins. For example, ASIC1 and -2 subunits, but not ASIC3, interact with PICK1 allowing for modulation by PKC [48], [49], [50]. On the other hand, ASIC2 and -3, and not ASIC1 subunits, interact with PSD-95 to effect subcellular localization [42], [46]. Other PDZ proteins that bind to the PDZ-binding motifs of various ASICs and modulate their function include CIPP, NHERF, LIN-7b, MAGI-1b, and PIST [46], [51], [52]. Other cytoplasmic regulatory domains within specific ASICs have also been described. Phosphorylation of Ser-25 within the N terminus of ASIC1a, and probably ASIC2a, by a PI3-kinase/Akt pathway regulates channel exocytosis [53]. A juxtamembrane region within the C terminus of ASIC1 is required for clathrin-dependent endocytosis [54]. Recent reviews describe additional examples [55], [56]. We found that coexpressing ASIC2 subunits in CHO cells increased surface expression of ASIC protein and increased current amplitudes, and perhaps the underlying mechanism involved ASIC2 interaction with endogenous cytosolic proteins. We speculate that heteromultimerization of different ASIC subunits increases the opportunity for interaction with multiple different cytosolic proteins.
Alternatively, heteromultimerization might be preferred in the biosynthesis, assembly, and/or trafficking of ASIC channels. Such is the case for the related epithelial Na+ channel (ENaC), a channel that transports Na+ to maintain normal salt and water homeostasis [57]. ENaC is composed of α, β, and γ subunits, and expression of all three subunits is necessary for maximal cell surface expression and function [58]. Studies of native acid-evoked currents in various populations of neurons support the idea that ASICs are also preferentially assembled as heteromultimers [3], [5], [7], [28], [29], [36], [37]. In the future it would be interesting to investigate if ASIC heteromultimerization alters the efficiency of channel processing within biosynthetic pathways.
Similar to its effect on ASIC3 [46], [59], we found that PSD-95 reduced cell surface expression and acid-evoked current amplitude in channels containing ASIC2. Consistent with previous work [42], mutation of the C-terminal PDZ-binding domain of ASIC2a abolished the capacity of PSD-95 to modulate ASIC2a. However, the mechanism by which PSD-95 decreases ASIC cell surface levels remains largely unknown. We previously demonstrated that PSD-95 modulation of ASIC3 was dependent upon their interaction within lipid rafts – membrane microdomains rich in cholesterol and sphingolipids that organize receptor/signaling complexes [59]. Moreover, our data suggested that most ASIC3 at the cell surface, independent of its interaction with PSD-95, is expressed within lipid raft membrane fractions [59]. Perhaps ASIC2 is similarly regulated by PSD-95 within lipid raft membrane microdomains.
Consistent with our data in heterologous cells, PSD-95 decreased acid-evoked current amplitude in hippocampal neurons in an ASIC2 dependent manner. Previous data showed that PSD-95 targeted ASIC2 to post-synaptic sites on dendritic spines [42]. We speculate that these results represent PSD-95 targeting ASIC expression to different locations with the neuron. PSD-95 organizes ion channels with their associated signaling partners at post-synaptic membranes, thus regulating the strength of synaptic activity [60]. ASICs are preferentially distributed in neuronal cell bodies, along dendritic shafts, and at dendritic spines [6], [61]. Since whole-cell patch-clamp of cultured neurons measures current through channels primarily expressed at the cell body, it is interesting to speculate that overexpression of PSD-95 signals the translocation of ASIC channels out of the cell body to dendritic spines.
In summary, accumulating evidence suggests that ASIC2 subunits are integral components of ASIC channels and contribute to normal brain function. Genetic deletion of ASIC2 in mice generates neurological behavior deficits that mirror those seen in mice lacking ASIC1a, which is the major pH-sensitive ion channel subunit in central neurons [38]. Moreover, recent human genetic linkage studies have associated the ASIC2 locus with multiple neurological disorders [39], [40], [41]. Heteromultimerization with ASIC2 subunits not only affects the biophysical properties of acid-evoked currents, but perhaps more importantly, our data here together with other recent studies suggest an important role for ASIC2 subunits in subcellular localization of the channels. Further studies of ASIC biosynthesis, assembly and trafficking will lend mechanistic insight into the role that ASICs play within the nervous system.
Acknowledgments
We thank Mara Zuckerman, Huiyu Gong and the DNA Core Facility (National Institute of Diabetes and Digestive and Kidney Diseases Grant DK-25295) for technical assistance.
Author Contributions
Conceived and designed the experiments: AH CB. Performed the experiments: AH NK TH MG CB. Analyzed the data: AH NK TH MG CB. Wrote the paper: AH CB.
References
- 1. Wemmie JA, Taugher RJ, Kreple CJ (2013) Acid-sensing ion channels in pain and disease. Nat Rev Neurosci 14: 461–471.
- 2. Jasti J, Furukawa H, Gonzales EB, Gouaux E (2007) Structure of acid-sensing ion channel 1 at 1.9 A resolution and low pH. Nature 449: 316–323.
- 3. Benson CJ, Xie J, Wemmie JA, Price MP, Henss JM, et al. (2002) Heteromultimers of DEG/ENaC subunits form H+-gated channels in mouse sensory neurons. Proc Natl Acad Sci U S A 99: 2338–2343.
- 4. Hesselager M, Timmermann DB, Ahring PK (2004) pH Dependency and desensitization kinetics of heterologously expressed combinations of acid-sensing ion channel subunits. J Biol Chem 279: 11006–11015.
- 5. Askwith CC, Wemmie JA, Price MP, Rokhlina T, Welsh MJ (2004) Acid-sensing ion channel 2 (ASIC2) modulates ASIC1 H+-activated currents in hippocampal neurons. J Biol Chem 279: 18296–18305.
- 6. Wemmie JA, Chen J, Askwith CC, Hruska-Hageman AM, Price MP, et al. (2002) The acid-activated ion channel ASIC contributes to synaptic plasticity, learning, and memory. Neuron 34: 463–477.
- 7. Wu LJ, Duan B, Mei YD, Gao J, Chen JG, et al. (2004) Characterization of acid-sensing ion channels in dorsal horn neurons of rat spinal cord. J Biol Chem 279: 43716–43724.
- 8. Zha XM, Wemmie JA, Green SH, Welsh MJ (2006) Acid-sensing ion channel 1a is a postsynaptic proton receptor that affects the density of dendritic spines. Proc Natl Acad Sci U S A 103: 16556–16561.
- 9. Coryell MW, Wunsch AM, Haenfler JM, Allen JE, McBride JL, et al. (2008) Restoring Acid-sensing ion channel-1a in the amygdala of knock-out mice rescues fear memory but not unconditioned fear responses. J Neurosci 28: 13738–13741.
- 10. Wemmie JA, Askwith CC, Lamani E, Cassell MD, Freeman JH Jr, et al. (2003) Acid-sensing ion channel 1 is localized in brain regions with high synaptic density and contributes to fear conditioning. J Neurosci 23: 5496–5502.
- 11. Ziemann AE, Allen JE, Dahdaleh NS, Drebot, II, Coryell MW, et al. (2009) The amygdala is a chemosensor that detects carbon dioxide and acidosis to elicit fear behavior. Cell 139: 1012–1021.
- 12. Xiong ZG, Zhu XM, Chu XP, Minami M, Hey J, et al. (2004) Neuroprotection in ischemia: blocking calcium-permeable acid-sensing ion channels. Cell 118: 687–698.
- 13. Ziemann AE, Schnizler MK, Albert GW, Severson MA, Howard MA 3rd, et al. (2008) Seizure termination by acidosis depends on ASIC1a. Nature neuroscience 11: 816–822.
- 14. Deval E, Noel J, Lay N, Alloui A, Diochot S, et al. (2008) ASIC3, a sensor of acidic and primary inflammatory pain. Embo J 27: 3047–3055.
- 15. Price MP, McIlwrath SL, Xie J, Cheng C, Qiao J, et al. (2001) The DRASIC Cation Channel Contributes to the Detection of Cutaneous Touch and Acid Stimuli in Mice. Neuron 32: 1071–1083.
- 16. Sluka KA, Price MP, Breese NM, Stucky CL, Wemmie JA, et al. (2003) Chronic hyperalgesia induced by repeated acid injections in muscle is abolished by the loss of ASIC3, but not ASIC1. Pain 106: 229–239.
- 17. Sutherland SP, Benson CJ, Adelman JP, McCleskey EW (2001) Acid-sensing ion channel 3 matches the acid-gated current in cardiac ischemia-sensing neurons. Proc Natl Acad Sci U S A 98: 711–716.
- 18. Waldmann R, Bassilana F, de Weille J, Champigny G, Heurteaux C, et al. (1997) Molecular cloning of a non-inactivating proton-gated Na+ channel specific for sensory neurons. J Biol Chem 272: 20975–20978.
- 19. Bassler EL, Ngo-Anh TJ, Geisler HS, Ruppersberg JP, Grunder S (2001) Molecular and functional characterization of acid-sensing ion channel (ASIC) 1b. J Biol Chem 276: 33782–33787.
- 20. Diochot S, Baron A, Salinas M, Douguet D, Scarzello S, et al. (2012) Black mamba venom peptides target acid-sensing ion channels to abolish pain. Nature 490: 552–555.
- 21. Donier E, Rugiero F, Jacob C, Wood JN (2008) Regulation of ASIC activity by ASIC4–new insights into ASIC channel function revealed by a yeast two-hybrid assay. Eur J Neurosci 28: 74–86.
- 22. Grunder S, Geissler HS, Bassler EL, Ruppersberg JP (2000) A new member of acid-sensing ion channels from pituitary gland. Neuroreport 11: 1607–1611.
- 23. Alvarez de la Rosa D, Zhang P, Shao D, White F, Canessa CM (2002) Functional implications of the localization and activity of acid-sensitive channels in rat peripheral nervous system. Proc Natl Acad Sci U S A 99: 2326–2331.
- 24. Price MP, Snyder PM, Welsh MJ (1996) Cloning and expression of a novel human brain Na+ channel. J Biol Chem 271: 7879–7882.
- 25. Waldmann R, Champigny G, Voilley N, Lauritzen I, Lazdunski M (1996) The mammalian degenerin MDEG, an amiloride-sensitive cation channel activated by mutations causing neurodegeneration in Caenorhabditis elegans. J Biol Chem 271: 10433–10436.
- 26. Babinski K, Catarsi S, Biagini G, Seguela P (2000) Mammalian ASIC2a and ASIC3 subunits co-assemble into heteromeric proton-gated channels sensitive to Gd3+. J Biol Chem 275: 28519–28525.
- 27. Bassilana F, Champigny G, Waldmann R, de WeilleJR, Heurteaux C, et al. (1997) The acid-sensitive ionic channel subunit ASIC and the mammalian degenerin MDEG form a heteromultimeric H+-gated Na+ channel with novel properties. J Biol Chem 272: 28819–28822.
- 28. Hattori T, Chen J, Harding AM, Price MP, Lu Y, et al. (2009) ASIC2a and ASIC3 heteromultimerize to form pH-sensitive channels in mouse cardiac dorsal root ganglia neurons. Circ Res 105: 279–286.
- 29. Gautam M, Benson CJ (2013) Acid-sensing ion channels (ASICs) in mouse skeletal muscle afferents are heteromers composed of ASIC1a, ASIC2, and ASIC3 subunits. Faseb J 27: 793–802.
- 30. Lu Y, Ma X, Sabharwal R, Snitsarev V, Morgan D, et al. (2009) The ion channel ASIC2 is required for baroreceptor and autonomic control of the circulation. Neuron 64: 885–897.
- 31. Price MP, Lewin GR, McIlwrath SL, Cheng C, Xie J, et al. (2000) The mammalian sodium channel BNC1 is required for normal touch sensation. Nature 407: 1007–1011.
- 32. Arnadottir J, Chalfie M (2010) Eukaryotic mechanosensitive channels. Annu Rev Biophys 39: 111–137.
- 33. Drew LJ, Rohrer DK, Price MP, Blaver KE, Cockayne DA, et al. (2004) Acid-sensing ion channels ASIC2 and ASIC3 do not contribute to mechanically activated currents in mammalian sensory neurones. J Physiol 556: 691–710.
- 34. Kang S, Jang JH, Price MP, Gautam M, Benson CJ, et al. (2012) Simultaneous disruption of mouse ASIC1a, ASIC2 and ASIC3 genes enhances cutaneous mechanosensitivity. PloS one 7: e35225.
- 35. Roza C, Puel JL, Kress M, Baron A, Diochot S, et al. (2004) Knockout of the ASIC2 channel in mice does not impair cutaneous mechanosensation, visceral mechanonociception and hearing. J Physiol 558: 659–669.
- 36. Baron A, Waldmann R, Lazdunski M (2002) ASIC-like, proton-activated currents in rat hippocampal neurons. J Physiol 539: 485–494.
- 37. Sherwood TW, Lee KG, Gormley MG, Askwith CC (2011) Heteromeric acid-sensing ion channels (ASICs) composed of ASIC2b and ASIC1a display novel channel properties and contribute to acidosis-induced neuronal death. J Neurosci 31: 9723–9734.
- 38.
Price MP, Gong H, Parsons MG, Kundert JR, Reznikov LR, et al.. (2013) Localization and behaviors in null mice suggest that ASIC1 and ASIC2 modulate responses to aversive stimuli. Genes Brain Behav.
- 39. Gregersen N, Dahl HA, Buttenschon HN, Nyegaard M, Hedemand A, et al. (2012) A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene. Eur J Hum Genet 20: 84–90.
- 40. Squassina A, Manchia M, Borg J, Congiu D, Costa M, et al. (2011) Evidence for association of an ACCN1 gene variant with response to lithium treatment in Sardinian patients with bipolar disorder. Pharmacogenomics 12: 1559–1569.
- 41. Stone JL, Merriman B, Cantor RM, Geschwind DH, Nelson SF (2007) High density SNP association study of a major autism linkage region on chromosome 17. Hum Mol Genet 16: 704–715.
- 42. Zha XM, Costa V, Harding AM, Reznikov L, Benson CJ, et al. (2009) ASIC2 subunits target acid-sensing ion channels to the synapse via an association with PSD-95. J Neurosci 29: 8438–8446.
- 43. Askwith CC, Cheng C, Ikuma M, Benson C, Price MP, et al. (2000) Neuropeptide FF and FMRFamide potentiate acid-evoked currents from sensory neurons and proton-gated DEG/ENaC channels. Neuron 26: 133–141.
- 44. Zha XM, Wang R, Collier DM, Snyder PM, Wemmie JA, et al. (2009) Oxidant regulated inter-subunit disulfide bond formation between ASIC1a subunits. Proceedings of the National Academy of Sciences of the United States of America 106: 3573–3578.
- 45. Benson CJ, Eckert SP, McCleskey EW (1999) Acid-evoked currents in cardiac sensory neurons: A possible mediator of myocardial ischemic sensation. Circ Res 84: 921–928.
- 46. Hruska-Hageman AM, Benson CJ, Leonard AS, Price MP, Welsh MJ (2004) PSD-95 and Lin-7b interact with ASIC3 and have opposite effects on H+-gated current. J Biol Chem 17: 17.
- 47. Kuryatov A, Gerzanich V, Nelson M, Olale F, Lindstrom J (1997) Mutation causing autosomal dominant nocturnal frontal lobe epilepsy alters Ca2+ permeability, conductance, and gating of human alpha4beta2 nicotinic acetylcholine receptors. J Neurosci 17: 9035–9047.
- 48. Baron A, Deval E, Salinas M, Lingueglia E, Voilley N, et al. (2002) Protein kinase C stimulates the acid-sensing ion channel ASIC2a via the PDZ domain-containing protein PICK1. J Biol Chem 277: 50463–50468.
- 49. Duggan A, Garcia-Anoveros J, Corey DP (2002) The PDZ domain protein PICK1 and the sodium channel BNaC1 interact and localize at mechanosensory terminals of dorsal root ganglion neurons and dendrites of central neurons. J Biol Chem 277: 5203–5208.
- 50. Hruska-Hageman AM, Wemmie JA, Price MP, Welsh MJ (2002) Interaction of the synaptic protein PICK1 (protein interacting with C kinase 1) with the non-voltage gated sodium channels BNC1 (brain Na+ channel 1) and ASIC (acid-sensing ion channel). Biochem J 361: 443–450.
- 51. Anzai N, Deval E, Schaefer L, Friend V, Lazdunski M, et al. (2002) The multivalent PDZ domain-containing protein CIPP is a partner of acid-sensing ion channel 3 in sensory neurons. J Biol Chem 277: 16655–16661.
- 52. Deval E, Friend V, Thirant C, Salinas M, Jodar M, et al. (2006) Regulation of sensory neuron-specific acid-sensing ion channel 3 by the adaptor protein Na+/H+ exchanger regulatory factor-1. J Biol Chem 281: 1796–1807.
- 53. Duan B, Liu DS, Huang Y, Zeng WZ, Wang X, et al. (2012) PI3-kinase/Akt pathway-regulated membrane insertion of acid-sensing ion channel 1a underlies BDNF-induced pain hypersensitivity. J Neurosci 32: 6351–6363.
- 54. Zeng WZ, Liu DS, Duan B, Song XL, Wang X, et al. (2013) Molecular mechanism of constitutive endocytosis of Acid-sensing ion channel 1a and its protective function in acidosis-induced neuronal death. J Neurosci 33: 7066–7078.
- 55. Baron A, Diochot S, Salinas M, Deval E, Noel J, et al. (2013) Venom toxins in the exploration of molecular, physiological and pathophysiological functions of acid-sensing ion channels. Toxicon 75: 187–204.
- 56. Zha XM (2013) Acid-sensing ion channels: trafficking and synaptic function. Mol Brain 6: 1.
- 57. Snyder PM (2002) The epithelial Na+ channel: cell surface insertion and retrieval in Na+ homeostasis and hypertension. Endocr Rev 23: 258–275.
- 58. Firsov D, Schild L, Gautschi I, Merillat AM, Schneeberger E, et al. (1996) Cell surface expression of the epithelial Na channel and a mutant causing Liddle syndrome: a quantitative approach. Proc Natl Acad Sci U S A 93: 15370–15375.
- 59. Eshcol JO, Harding AM, Hattori T, Costa V, Welsh MJ, et al. (2008) Acid-sensing ion channel 3 (ASIC3) cell surface expression is modulated by PSD-95 within lipid rafts. Am J Physiol Cell Physiol 295: C732–739.
- 60. Kim E, Sheng M (2004) PDZ domain proteins of synapses. Nat Rev Neurosci 5: 771–781.
- 61. Jovov B, Tousson A, McMahon LL, Benos DJ (2003) Immunolocalization of the acid-sensing ion channel 2a in the rat cerebellum. Histochem Cell Biol 119: 437–446.