Introduction

The stress, referring to a series of physiological and psychological reactions in response to external environmental changes or internal conflicts that threaten the homeodynamic equilibrium, is tightly controlled by neural systems that effectively switch vital physiological functions between homeostatic operation and emergency response. When an individual experiences extreme stressors that are out of their control, its stress response gets activated, which could lead to agitation and eventually stress-related disorders such as anxiety, depression, diabetes and hypertension [1,2,3,4].

The hypothalamic-pituitary-adrenal (HPA) axis is crucial for maintaining internal homeostasis through its modulation of stress in the central nervous system. It has been well documented to be the major component of the neuroendocrine network responding to both acute and chronic stress [2, 5, 6]. The corticotropin-releasing hormone (CRH) neuron in the paraventricular nucleus (PVN) of the hypothalamus controls HPA axis activity through initiating a hormonal cascade. Stress activates the CRH neuron, which results in the production and release of CRH into the pituitary, subsequently promoting the elevation of serum ACTH and corticosterone levels. Moreover, CRH neurons in the PVN (CRHPVN neurons) receive and send projections to neighboring and extra-hypothalamic regions, modulating the activities of the autonomic nervous system and other stress circuits involved in controlling stress [7,8,9,10]. Therefore, the CRHPVN neuron is a key player in orchestrating stress response [2, 8, 11].

Neuronal activities of CRHPVN neurons are determined by ion channels and receptors expressed on the cell membrane of these neurons such as NMDA receptor [12], GABAA receptor [13], AMPA receptor [3, 14] and voltage-gated potassium channel [15, 16]. Emerging evidence suggest that newly identifying ion channels and receptors are involved in precise mechanisms governing the elevated CRHPVN neuronal activity in response to various stressors. Acid-sensing ion channels (ASICs), members of the epithelial Na+ channel/degenerin (ENaC/DEG) family, are proton-gated cationic channels. ASIC family consists of six subtypes including ASIC1a, 1b, 2a, 2b, 3, and 4 that are encoded by four genes. ASIC1a has a unique feature of Ca2+-permeability compared to the other ASIC subtypes. The activation of ASIC1a leads to increased membrane excitability and Ca2+ influx, which contributes to neuronal plasticity [17, 18]. Moreover, ASIC1a is associated with a variety of intracellular signaling molecules such as cAMP/PKA [19], Ca2+/CaMKII [20,21,22], NF-κB [23,24,25,26] and c-Fos [27]. These signaling molecules have been demonstrated to regulate CRH gene transcription in the PVN [28,29,30] and are involved in stress modulation [29].

Notably, ASIC1a is proven to be expressed in brain regions associated with stress modulation including amygdala, hippocampus, bed nucleus of the stria terminalis, nucleus accumbens and PVN [18, 31]. A variety of studies have demonstrated the involvement of ASIC1a in stress-related behaviors. Downregulation and inhibition of ASIC1a in the amygdala produce antidepressant-like effects [32]. Pharmacological inhibition and genetic knockdown of ASIC1a in the central nucleus of amygdala has shown to ameliorate anxiety-related behaviors [33]. Moreover, ASIC1a increases inhibitory activity in the basolateral amygdala and decreases anxiety during estrus [34]. Targeting ASIC1a gene or acutely inhibiting ASIC1a suppresses fear and anxiety independent of conditioning [27]. Additionally, overexpression of ASIC1a in transgenic mice increases fear conditioning [35]. Our recent study has indicated the presence of ASIC1a in the PVN [36, 37] and inhibition of ASICs may act on the HPA axis to alleviate the depression-related behavior in the chronic stress-subjected rat [37]. Nevertheless, whether ASIC1a in the PVN are involved in the modulation of HPA axis and mood behaviors remains unknown. Therefore, the present study aimed to investigate the specific role of ASIC1a in the PVN in regulating HPA axis function and anxiety- and depression-related behaviors.

Materials and methods

Animals

The C57BL/6J and Crh-Cre male mice used in this study were 6 to 8 weeks old unless otherwise stated. The C57BL/6J mice were purchased from SiPeiFu (Cat#B205, Beijing, China), and Crh-Cre mice were gifts from Prof. Ji Liu. The animals were bred in the facility at 22 °C and 35–55% humidity. They were maintained under a 12-h light/dark cycle (lights on from 8:00 am to 8:00 pm) with water and food available ad libitum. In order to avoid changes caused by the estrus cycle, we only considered male mice in the experiments. Animals were randomly assigned to control and treatment groups. All investigators were blinded to group allocation during data collection and analysis, group size was selected based on published reports in the field.

Virus injection

The PVN injection was performed using a stereotactic frame (RWD, Shenzhen, China) under anesthesia with an intraperitoneal injection of pentobarbital sodium (20 mg/kg, i.p.). A volume of 100 nL virus was injected through calibrated glass microelectrodes connected to an infusion pump (micro4, WPI, USA) at a rate of 30 nL/min. The injection coordinates for the PVN were as follows: antero-posterior (AP), −0.79 mm from bregma; medio-lateral (ML), ±0.26 mm from the midline; dorsal-ventral (DV), −4.55 mm from the brain surface. The pipette remained in the injection site for 5–10 min at the end of infusion to avoid virus overflow.

To label CRH neurons, rAAV-Ef1α-DIO-EGFP-WPRE-pA (AAV-DIO-GFP, AAV2/9, 1.95 × 1012 vg/mL, Cat# PT-0795, BrainVTA, Wuhan, China) was injected into the PVN. For local knockdown of ASIC1a in CRH neurons within the PVN, recombinant viruses rAAV-CMV-DIO-mCherry-U6-shRNA (ASIC1a) (AAV-shASIC1a, AAV2/9, 5.00 × 1012 vg/mL, BrainVTA, Wuhan, China) were used. The viruses rAAV-CMV-DIO-mCherry-U6-shRNA (scramble) (AAV-mCherry, AAV2/9, 5.20 × 1012 vg/mL, Cat# PT-2788, BrainVTA, Wuhan, China) were used as controls. The complete sequences of the constructs in the supplemental material in Supplementary Data 1. The viral expression was checked after sacrificing of animals, and data were collected only from animals with correct viral expression. Initially, eleven mice were used in the experiment, one was excluded due to incorrect viral expression location, therefore, data from ten mice were used for the analysis of the results.

Immunohistochemistry and imaging

Mice were deeply anesthetized by intraperitoneal injection with pentobarbital sodium, then perfused with ice-cold 0.9% saline followed by 4% paraformaldehyde (PFA). The brains were removed and placed in 4% PFA in PBS at 4 °C overnight, and then incubated in 30% (w/v) sucrose until they sank. Coronal slices were cut using a cryostat (CM1860, Leica, Germany) to a thickness at 40 µm. For immunofluorescence staining, the sections were incubated with blocking buffer (0.4% Triton X-100 plus 5% goat serum in PBS) for 1 h at room temperature, and then they were treated with primary antibodies diluted with blocking solution, including anti-c-Fos (1:500, rabbit, Cat# ab190289, Abcam, Cambridge, UK), anti-ASIC1a (1:500, guinea pig, Cat# ASC-014-GP, Alomone Labs, Jerusalem, Israel) at 4 °C for 24 h. After three washes with PBS, the slices were incubated with the corresponding fluorophore-conjugated secondary antibodies (1:500, Invitrogen, MA, United States) for 1.5 h at room temperature. Finally, sections were washed 3 × 5 min with PBS followed by mounting on slides with 80% glycerol solution. All sections were photographed by confocal microscopy (LSM980, Zeiss).

Cannula infusion

Mice were anesthetized with isoflurane during the infusion, and the drug PcTx1 (15 μM in ACSF, 100 nL per side, Peptide Institute, Osaka, Japan) was administered through a polyethylene tubing between the injector and control infusion pump, and ACSF (100 nL) was locally applied as control. For intracranial microinfusion, the guide cannula (internal diameter 0.35 mm, RWD) was generally implanted 0.2 mm higher than the target nucleus of the PVN in mice one week before behavioral tests to ensure sufficient recovery time. After surgery, mice were housed individually. The cannula location was checked after sacrificing of animals, and data were collected only from animals with proper placement. Initially, eight mice were used in the experiment, one was excluded due to incorrect cannula placement, therefore, data from seven mice were used for the analysis of the results.

Behavioral tests

Open-field test (OFT)

A white behavior test box (40 × 40 × 40 cm, length × width × height) was virtually divided into a center field (center, 20 × 20 cm) and a periphery field. For each test, the mice were placed in the periphery, and the locomotion of the animal was recorded with a video camera for 6 min. The time spent in the center or peripheral area was subsequently measured offline using EthoVision XT software (Noldus). We cleaned the instrument with 75% ethanol after each test to eliminate the odor effect.

Elevate plus maze (EPM)

An apparatus consisting of a central platform (6 × 6 cm) and two open arms (30 × 6 cm) orthogonal to two closed arms (30 × 6 × 20 cm) was placed 100 cm above the floor. Each animal was placed on the central platform facing one of the open arms and allowed to freely explore the maze for 6 min. The mice movement trajectory was recorded from above with a video camera. The time spent in the open arms was recorded and calculated offline using EthoVision XT software (Noldus). We cleaned the instrument with 75% ethanol after each test to eliminate the odor effect.

Tail suspension test (TST)

The mice were suspended by their tails, approximately 33 cm above the floor. Each mouse was affixed to a hook positioned 1 cm from the tail tip using tape. A test period of 6 min was recorded, during which the duration of immobility was measured. For the TST, the results were calculated by researchers who were blind to the experiment. Immobility was defined as the absence of any observable movement except for whisker movement and respiration.

Forced swimming test (FST)

The mice were placed into a circular bucket (height, 25 cm; diameter, 10 cm), filled with water (15-cm depth) maintained at 24–26 °C. They were placed in the container with their backs to the wall and the front paws touching the water, and allowed to swim freely for 6 min. After each session, the mouse was dried with a towel and then returned to its home cage. For the FST, the results were calculated by researchers who were blind to the experiment. Each mouse was judged to be immobile when it ceased struggling and remained floating motionless in the water, making only those movements necessary to keep its head above water. For behavior tests, the data of the mice that did not move throughout the entire test were excluded. All behavioral data were included in the analysis, no data were excluded due to immobility.

Hormone measurement

For the animal experiment, blood samples were collected via the ocular vein after 0.5 h of FST stimulation between 11:00 a.m. and 1:00 p.m. The blood was centrifuged (1500 g, 15 min) for plasma, and then stored at −80 °C for subsequent testing. A panel of hormones associated with stress was measured using ELISA kits for ACTH (Cat. D721184, BBI-life sciences) and corticosterone (Cat. D721183, BBI-life sciences). For the cell experiment, the release level of CRH was measured using ELISA kits for human (Cat# MM-1014H1, MEIMIAN, Jiangsu, China) and for mice (Cat# MM-0509M1, MEIMIAN, Jiangsu, China). The experiments were conducted according to the manufacturer’s instructions provided with the kit.

Ca2+ imaging and fiber photometry

The virus rAAV-hSyn-DIO-GCaMP6s-WPREs (AAV-DIO-GCaMP6s, AAV2/9, 1.20 × 1013 vg/mL, 200 nL, Cat# PT-0091, BrainVTA, Wuhan, China) was unilaterally injected in the PVN of Crh-Cre mouse and allowed to express for 3 weeks. An optical fiber (250 μm diameter core, NA 0.37, Newdoon, Hangzhou, China) was placed on the PVN of Crh-Cre male mouse and connected to a fiber photometry system (ThinkerTech, Nanjing, China). The excitation light was generated by a 480-nm LED, reflected with a dichroic mirror, and delivered to the brain to excite the GCaMP6. The excitation light was passed through another band-pass filter, into a complementary metal-oxide semiconductor detector (DCC3240M, Thorlabs), and finally recorded by a LabVIEW program (SingleColorMultiChannel Acquisition Software, ThinkerTech, Nanjing, China).

Fiber photometry signals were processed with acustom-written MATLAB software, which is available at https://zenodo.org/record/6456623#.YlaF_8hByUk (Zenodo ID: 6456623; Zenodo DOI: 10.5281/zenodo.6456623; ThinkerTech Nanjing Bioscience, 2020). Briefly, all the data were segmented on the basis of behavioral events and baseline phase. The values of Ca transients change (ΔF/F) from −2 s to 6 s (0 s represents the onset of each stimulus), where ΔF/F = (F-F0)/F0 for each trial and F0 was defined as the average value in control time. For fiber photometry, data of the mice from loss of the optical fiber and incorrect optical fiber or viral expression were excluded. All of the data were included in the analysis, no data were excluded due to incorrect optical fiber.

Cell culture

Human neuroblastoma cell line BE (2)-C was cultured in DMEM (VivaCell Biosciences, Shanghai, China) supplemented with 10% FBS (ExCell Bio, Suzhou, China) and 1% P/S (Biosharp, Hefei, China) at 37 °C, containing 5% CO2. Primary hypothalamic neurons were prepared as previously described [38]. At day 7 of neuronal culturing, lentiviral overexpression or knockdown of ASIC1a was introduced, and the cells were subsequently cultured for an additional 48 h for experimentation.

Plasmid and lentiviral construction

For knockdown experiments, shRNA sequences were cloned into pGreenPuro hairpin lentivector (SBI, California, USA) separately, targeting human ASIC1a (5’-3’: CTATGGAAAGTGCTACACGTT) and mouse ASIC1a (5’-3’: CCTCAAGCATACGGAATCT). Overexpression vectors were generated by inserting human/mouse ASIC1a sequence into pLVX-Green1-N1 vector. All plasmids were constructed using restriction enzyme digestion (Yugong Biolabs, Jiangsu, China) and T4 ligation (Monad Biotech, Suzhou, China) methods, and were confirmed by Sanger sequencing. Lentiviral particles were produced by transient co-transfection of the aforementioned constructed plasmids along with pCMV-dR8.2 and pVSV-G into 293 T cells, followed by the collection of viral particles through ultracentrifugation.

Western blot assay

The cells were lysed on ice using 1% Triton X-100 in PBS, followed by sonication and centrifugation at 13,400 g for 15 min at 4 °C. The supernatant was then subjected to SDS-PAGE and transferred onto nitrocellulose membranes (running buffer: 0.025 M Tris, 0.25 M Glycine, 0.1% SDS; transfer buffer: 25 mM Tris, 192 mM Glycine, 20% Methanol). After blocking (5% skimmed milk), the membranes were incubated with primary antibodies overnight, including that CRH/CRF Polyclonal antibody (Cat#10944-1-AP, Proteintech, Wuhan, China), ASIC1a Polyclonal antibody (Cat#27235-1-AP, Proteintech, Wuhan, China), c-Fos monoclonal antibody (Cat#66590-1-Ig, Proteintech, Wuhan, China), phospho-CaMKII alpha/delta (Thr286) antibody (Cat#AF3493, Affinity Biosciences, Jiangsu, China) and CaMKII α antibody (Cat#WL03453, Wanlei Bio, Shenyang, China), and β-actin antibody (Cat#WL01372, Wanlei Bio, Shenyang, China), and then followed by HRP-conjugated secondary antibodies (1:5000). ECL reagent (US Everbright) was added, and the bands were visualized using a chemiluminescence imager (Cat#SH-523, SHST, Hangzhou, China). The dilution of antibodies was conducted according to the manufacturer’s instructions.

RNA extraction and qPCR

Total RNA was extracted using the Trizol reagent kit (Invitrogen, USA), followed by reverse transcription using a reverse transcription kit (Vazyme, Nanjing, China). RT-qPCR was conducted on the QuantStudio 3 platform. All experiments were conducted following the manufacturer’s instructions.

qPCR primer:

CRH F: 5’-3’ CAGCCCTTGAATTTCTTGCAG,

CRH R: 5’-3’ GACTTCTGTTGAGATTCCCCAG,

ASIC1a F: 5’-3’ GGAAGTGCCAGAAGGAGG,

ASIC1a R: 5’-3’ GCGGGATGGTGAGGTAGGAT,

c-Fos F: 5’-3’ CCAGCATGGGCTCTCCTGTCAACACA,

c-Fos R: 5’-3’ TCCGTAAGGATGGGGCGCTCTGGT,

β-actin F: 5’-3’ CATTGCTGACAGGATGCAGAAGG,

β-actin R: 5’-3’ TGCTGGAAGGTGGACAGTGAGG

Neuron transfection and calcium imaging

Calcium phosphate transfection was performed in cultured hypothalamic neurons grown on confocal dishes on day in vitro (DIV) 7–10. Before transfection, the culture medium was replaced with fresh Neurobasal medium, and the original medium was retained. For each dish, 2 μg of GCaMP6 plasmid together with 2 μg other plasmids (vector, mCherry-ASIC1a, or shASIC1a) was diluted in 60 μL CaCl2 solution (0.3 M) with pipetting. An equal volume (60 μL) of HBSS (280 mM NaCl, 1.5 mM Na2HPO4, 50 mM HEPES, pH 6.9) was then added. The mixture was combined immediately by gentle pipetting and promptly transferred into the dish. After incubation at 37 °C for 1–1.5 h, the medium was replaced with CO2-saturated Neurobasal medium (washing medium) to remove excess calcium phosphate precipitates. Finally, the washing medium was replaced with a 1:1 mixture of the original conditioned medium and fresh Neurobasal medium supplemented with B27, and the dish was returned to the culture incubator.

Calcium imaging was conducted at DIV 14–16, in transfected neurons. Confocal dishes with transfected neurons were mounted in a standard extracellular solution and imaged consecutively using a Nikon A1R laser scanning confocal microscope with a 20 × objective. GCaMP6 was excited using a 488 nm laser, and mCherry (used to label transfected neurons) was excited with a 561 nm laser. Following a 30-s baseline recording at pH 7.4, the perfusate was rapidly switched to pH 6.5 for 20 s, followed by a return to pH 7.4 for an additional 60 s. GCaMP6 fluorescence change representing intracellular Ca2+ dynamics was calculated as F/F0, where F0 represents the median fluorescence intensity during the 30-s baseline period. For cell calcium imaging, low transfection efficiency were excluded. All of the data were included in the analysis, no data were excluded.

Statistical analysis

The statistical analyses and graphing were performed using GraphPad Prism 8.0 (GraphPad Software, Inc., San Diego, CA, USA) or SPSS (version 18, IBM, Chicago, IL, USA). Normality of data was checked with the Shapiro-Wilk test and homoscedasticity was checked using Bartlett’s test. For statistical comparisons, a two-tailed unpaired t test was used to compare two groups. One- and two-way ANOVA tests followed by post hoc analyses were used to statistically analyze the data from the experimental groups with multiple comparisons. All experiments were repeated in at least three independent biological replicates. Statistical significance levels are indicated as *p < 0.05; **p < 0.01; ***p < 0.001, ****p < 0.0001; n.s. indicates not statistically significant. All data are expressed as the mean ± SEM. Potential outliers were assessed using Grubbs’ test, and no statistically significant outliers were identified.

Results

Morphological evidence of ASIC1a in the PVN, whose blockade reduced HPA axis activity and improved anxiety- and depressive-like behaviors

Consistent with previous studies [36, 37], the expression of ASIC1a in the PVN was confirmed by immunofluorescence staining (Fig. 1A). The specificity of the antibodies used in this study was validated via immunofluorescence and Western blotting. No ASIC1a signal was detected in the brains of ASIC1a knockout mice (Supplementary Figure 1A), and Western blotting with an anti-ASIC1a antibody identified a single band at ~60 kD (Supplementary Figure 1B). In order to evaluate whether ASIC1a in the PVN modulates the stress response, PcTx1, a specific ASIC1a inhibitor, was bilaterally infused into the PVN through implanted catheters in naïve mice, followed by behavioral assessments. As a control, an identical procedure was performed using artificial cerebrospinal fluid(ACSF) as the vehicle solution (Fig. 1B, C and Supplementary Figure 1C). The PcTx1 group exhibited a significant increase in the time spent in the center of the open-field test (OFT) and the open arms of the elevated plus maze (EPM) compared to the ACSF group (Fig. 1D, E). However, no significant differences were observed between the two groups in terms of total distance traveled or average speed in either the OFT or EPM (Supplementary Figure 2A–D). In the tail suspension test (TST) and forced swimming test (FST), the PcTx1 group showed a significant reduction in immobility time (Fig. 1F, G). Additionally, plasma ACTH and corticosterone levels were significantly decreased in the PcTx1 group following acute stress challenges (Fig. 1H–J), while baseline plasma ACTH and corticosterone levels prior to stress showed no significant differences between the two groups (Supplementary Figure 2E, F). Finally, we observed a significant reduction in c-Fos expression specifically within ASIC1a-positive neurons in the PVN of PcTx1-treated mice compared to controls after FST stimulation (Supplementary Figure 2G, H).

Fig. 1: Inhibition of ASIC1a in the PVN ameliorated anxiety- and depression-like behaviors and decreased HPA axis activity.
Fig. 1: Inhibition of ASIC1a in the PVN ameliorated anxiety- and depression-like behaviors and decreased HPA axis activity.
Full size image

A Representative immunofluorescence image for ASIC1a (red) in the PVN from a naïve mouse. Scale bar, 100 μm. B Schematic of bilateral cannula injection sites into the paraventricular nucleus (PVN) (coordinates: anterior-posterior = –0.79, medial-lateral = ±0.26, dorsal-ventral = –4.35). C Schematic of pharmacological experimental procedure. D The bar graph illustrates the behavioral analysis, showing that the PcTx1 group exhibited a significant increase in the time spent in the center of the open-field test (OFT) compared to the ACSF group (n = 7 per group). *p < 0.05 (unpaired t-test). E The bar graph illustrates the behavioral analysis, showing that the PcTx1 group exhibited a significant increase in the time spent in the open arms of the elevated plus maze (EPM) compared to the ACSF group (n = 7 per group). *p < 0.05 (unpaired t-test). F The bar graph illustrates the results of the tail suspension test (TST), showing that the PcTx1 group exhibited a significant reduction in immobility time compared to the ACSF group (n = 7 per group). *p < 0.05 (unpaired t-test). G The bar graph illustrates the results of the forced swimming test (FST), showing that the PcTx1 group exhibited a significant reduction in immobility time compared to the ACSF group (n = 7 per group). *p < 0.05 (unpaired t-test). H Experimental paradigm for blood collection after forced swimming. I The bar graph illustrates plasma ACTH levels in the PcTx1 group and ACSF group following stress stimulation (n = 6 per group). *p < 0.05 (unpaired t-test). J The bar graph illustrates plasma corticosterone levels in the PcTx1 group and ACSF group following stress stimulation (n = 6 per group). *p < 0.05 (unpaired t-test). See also Supplementary Data 2.

Knockdown of ASIC1a decreased the CRHPVN neuronal activity and ameliorated anxiety- and depression-related behaviors

Since CRHPVN neurons serve pivotal roles in the modulation of stress, we first examined whether these neurons express ASIC1a. By injecting AAV-DIO-mCherry into the PVN of Crh-Cre mice (Fig. 2A), immunofluorescence staining showed that ASIC1a was highly co-labeled with the mCherry + CRHPVN neurons (Fig. 2B, C). To further explore the role of ASIC1a in the CRHPVN neurons, we designed a Cre-dependent AAV vector expressing ASIC1a-targeting short-hairpin RNAs (shRNAs) for knockdown experiments. Two recombinant adeno-associated viruses (rAAVs) were used in Crh-Cre mice: rAAV-CMV-DIO-mCherry-U6-shRNA (ASIC1a) (AAV-shASIC1a) and rAAV-CMV-DIO-mCherry-U6-shRNA (scramble) (AAV-mCherry) as a control (Fig. 2D, E). The AAV-shASIC1a construct utilized the U6 promoter to drive ASIC1a-specific shRNA expression, leading to post-transcriptional silencing of ASIC1a. The CMV-DIO-mCherry cassette ensured Cre-dependent expression of the fluorescent reporter mCherry, allowing visualization of transfected neurons and confirmation of ASIC1a knockdown specificity. In contrast, the AAV-mCherry construct expressed a scrambled shRNA sequence under the U6 promoter, serving as a negative control without altering ASIC1a expression. Four weeks after virus injection PVN, Western blot analysis demonstrated a significant reduction in ASIC1a protein levels in the AAV-shASIC1a group compared to the AAV-mCherry group (Fig. 2F, G). Immunofluorescence staining further confirmed reduced ASIC1a expression in the AAV-shASIC1a group (Fig. 2H). Behavior tests showed that CRHPVN neuron-specific ASIC1a knockdown led to increased times in the central area of the OFT and the open arms of the EPM (Fig. 3A, B). No significant differences were observed between groups in total distance traveled or average speed in the OFT and EPM (Supplementary Figure 3A–D). Additionally, mice with ASIC1a knockdown exhibited significantly reduced immobility time in the TST and FST compared to controls (Fig. 3C, D). Plasma ACTH and corticosterone levels were also significantly decreased in the AAV-shASIC1a group following acute stress challenges (Fig. 3E–G), while baseline levels prior to stress showed no significant differences between the two groups (Supplementary Figure 3E, F).

Fig. 2: ASIC1a neurons in the PVN that co-localize with CRH neurons.
Fig. 2: ASIC1a neurons in the PVN that co-localize with CRH neurons.
Full size image

A Experimental paradigm for viral injection of AAV-DIO-mCherry in Crh-Cre mice. B, C Representative images (B) and statistical data (C) showing ASIC1a (green) neurons in the PVN co-localized with CRH (red) neurons. Scale bars, 50 μm. D Experimental paradigm for viral injection of AAV-DIO-shRNA in Crh-Cre mice. E Schematic illustration of the construction strategy for ASIC1a knockdown. F, G Representative Western blot images (F) and quantification (G) demonstrating that AAV-DIO-shASIC1a injection reduced ASIC1a expression in the PVN (n = 6 per group). *p < 0.05 (unpaired t-test). H Immunofluorescence images showing mCherry-positive neurons co-labeled with ASIC1a in the AAV-mCherry and AAV-shASIC1a groups. Scale bars, 50 μm. See also Supplementary Data 2.

Fig. 3: Knockdown of ASIC1a decreased the CRHPVN neuronal activity and ameliorated anxiety- and depression-related behaviors.
Fig. 3: Knockdown of ASIC1a decreased the CRHPVN neuronal activity and ameliorated anxiety- and depression-related behaviors.
Full size image

A-D Behavioral effects of the genetic knockdown of ASIC1a in CRHPVN neurons. Figure 3A shows the open-field test (OFT), Fig. 3B shows the elevated plus maze (EPM), Fig. 3C shows the tail suspension test (TST), and Fig. 3D shows the forced swimming test (FST), demonstrating significant behavioral differences between the AAV-mCherry group and the AAV-shASIC1a group (n = 10 per group). *p < 0.05, **p < 0.01 (unpaired t-test). E Experimental paradigm for blood collection following forced swimming. F, G Plasma ACTH levels (F) and corticosterone levels (G) were significantly reduced in the AAV-shASIC1a group compared to the AAV-mCherry group after forced swimming (n = 6 per group). *p < 0.05, **p < 0.01 (unpaired t-test). H Schematic of the real-time optical fiber photometry assay. I Experimental paradigm for viral injection of AAV-shRNA and AAV-DIO-GCaMP6s in Crh-Cre mice. J, K Representative images (J) and statistical data (K) showing AAV-shRNA and AAV-DIO-GCaMP6s expression in the PVN. Scale bars, 50 μm. L-O Calcium activity analysis of CRHPVN neurons in the AAV-shASIC1a group compared to the AAV-mCherry group. Figure 3L shows average calcium activity, Fig. 3M shows the area under the curve, Fig. 3N shows the maximum peak value, and Fig. 3O shows calcium signals at specific time points (n = 5 per group). *p < 0.05, **p < 0.01 (unpaired t-test and two-way ANOVA). See also Supplementary Data 2.

To examine the effects of ASIC1a on the activity of CRHPVN neurons, fiber photometry recordings were performed in mice injected with virally expressed fluorescent Ca2+ indicator GCaMP6s (AAV-DIO-GCaMP6s) mixed with either AAV-shASIC1a or AAV-mCherry into the PVN. A foot shock was applied to activate CRHPVN neurons (Fig. 3H, I). Co-localization of red fluorescent protein with green fluorescence confirmed successful targeting of CRHPVN neurons (Fig. 3J, K). In response to foot shock, bulk Ca2+ signals (ΔF/F) in the AAV-mCherry group showed overall > 30% change, whereas the AAV-shASIC1a group exhibited about 10% changes (Fig. 3L). Analysis of the area under the curve, peak amplitude, and specific time points revealed statistically significant differences between the two groups (Fig. 3M–O), indicating that ASIC1a knockdown attenuates neuronal activity in response to acute stress. Similarly, during the FST, bulk Ca2+ signals in the AAV-shASIC1a group were decreased compared to the AAV-mCherry group (Supplementary Figure 4A, B), with reduced area under the curve and peak amplitude specifically associated with struggling behavior (Supplementary Figure 4C, D). Consistent with these findings, c-Fos analysis after forced swimming showed a significant reduction in c-Fos expression within the mCherry-positive cells in the AAV-shASIC1a group, with no significant change in the mCherry-negative cells between two groups (Supplementary Figure 4E–G). Western blot analysis demonstrated a significant reduction in CRH protein levels in the PVN of AAV-shASIC1a group compared to the AAV-mCherry group following exposure to the forced swim test (Supplementary Figure 4H, I).

ASIC1a modulated CRH expression and secretion

To investigate the mechanisms underlying the effects of ASIC1a on CRH expression and release, the neuroblastoma cell line BE (2)-C cells were treated with Hanks’ balanced salt solution (HBSS) at pH 6.5 [22, 39,40,41,42,43] for 5 min [44], followed by a return to normal serum-free culture medium. This acid treatment significantly enhanced CRH secretion, with a notable peak at 60 min post-acid treatment, where the mean CRH concentration surged from 13.9 pg/mL to 17.79 pg/mL. In contrast, the administration of ASIC1a blockers PcTx1 or amiloride attenuated this response, moderating the mean CRH concentrations to 15.13 pg/mL and 15.29 pg/mL, respectively. Quantitative assessments were performed at intervals spanning from 1 min to 24 h following the treatment (Fig. 4A). This finding was further validated in primary cultured hypothalamic neurons. Following a 5-minute acid treatment and a subsequent 3-hour post-acid incubation, the mean concentration of CRH secreted by neurons increased from 15.43 pg/mL to 20.12 pg/mL. In contrast, the PcTx1 treatment group maintained a stable CRH level of 15.42 pg/mL (Fig. 4B). ASIC1a knockdown also significantly attenuated the acid-induced increase in CRH release, with the mean CRH secretion level reduced from 31.58 pg/mL to 27.88 pg/mL 3 h after acid treatment in primary neurons (Fig. 4C). Immunofluorescence staining demonstrated a significant upregulation of CRH expression in BE (2)-C cells treated with acidic HBSS for 30 min where ASIC1a was overexpressed (Fig. 4D, E), and this effect was inhibited by both PcTx1 and amiloride in cultured hypothalamic neurons at both protein and mRNA levels (Fig. 4F–H).

Fig. 4: ASIC1a modulated CRH expression and secretion.
Fig. 4: ASIC1a modulated CRH expression and secretion.
Full size image

A The heatmap shows the release levels of CRH in BE (2)-C cell culture supernatants detected by ELISA. The BE (2)-C cells were treated with HBSS with a pH of 6.5 for 5 min or pretreated with 100 nM PcTx1 or 200 nM amiloride for 5 min and maintained in HBSS pH 6.5. The supernatants were collected at 1, 15, 30, 60, 90, 120, 180 min, 12 h, and 24 h for detection. The experiment was conducted with three independent biological replicates, ensuring the presence of the drug throughout both the culture and acid treatment stages (n = 3 per group). *p < 0.05, ***p < 0.001, ****p < 0.0001 (two-way ANOVA). B The bar graph shows CRH release levels in neuronal culture supernatants detected by ELISA. The experimental treatments were conducted as in Fig. 4A, and supernatants were collected at 3-h time point for detection (n = 3 per group). **p < 0.01 (one-way ANOVA). C The bar graph shows CRH levels in the supernatant of ASIC1a knockdown neuronal culture medium detected by ELISA after HBSS pH 6.5 treatment and the supernatants were collected at 3-h time point for detection (n = 3 per group). *p < 0.05 (unpaired t-test). D Representative confocal images (scale bar = 5 μm) of CRH in BE (2)-C cells overexpressing GFP/ASIC1a-GFP for 48 h, before or 30 min after treatment with HBSS at pH 6.5. E The bar graph illustrates the relative fluorescence intensity of CRH shown in Fig. 4D (n = 3 per group). *p < 0.05, ****p < 0.0001 (one-way ANOVA). F Representative western blot assay showing the protein expression levels of CRH in primary hypothalamic neurons. Experimental treatments were conducted as in Fig. 4A, and the cells were detected at the 3-h time point. G The bar graph illustrates the grayscale scanning analysis of Fig. 4F, showing the relative expression levels of CRH (n = 3 per group). **p < 0.01 (one-way ANOVA). H The bar graph shows the mRNA expression levels of CRH in primary hypothalamic neurons detected by qPCR. Experimental treatments were conducted as in Fig. 4F (n = 3 per group). ****p < 0.0001 (one-way ANOVA). See also Supplementary Data 2.

ASIC1a facilitated CRH transcription via Ca2+/CaMKII/c-Fos pathway

As a Ca2+-permeable cation channel, ASIC1a activation was hypothesized to modulate CRH mRNA expression via increasing intracellular Ca2+ concentration. We performed Ca2+ imaging experiments to show that application of the acidic solution (pH 6.5) elicited a rise in intracellular Ca2+ in cultured mouse hypothalamic neurons. This response was enhanced by ASIC1a overexpression and diminished by ASIC1a knockdown or application of the inhibitors PcTx1 and amiloride (Fig. 5A, Supplementary Figure 5A, B). Further analysis revealed that ASIC1a activation significantly influenced the expression of Ca2+ signaling-related proteins. Acid stimulation led to a marked elevation in phosphorylated CaMKII levels and a concomitant increase in c-Fos protein levels (Fig. 5B–D). This upregulation of c-Fos occurred at the transcriptional level (Fig. 5E). Given that c-Fos is a critical effector of Ca2+ signaling known to regulate CRH expression [45], we confirmed its close association with ASIC1a activation via immunofluorescence (Fig. 5F, G). Activator protein-1 (AP-1) is a complex of c-Fos and c-Jun. The AP-1 inhibitor T-5224, which specifically inhibits the DNA binding activity of AP-1 [46,47,48,49]. Since AP-1 is a complex containing c-Fos, it is plausible that T-5224 may also inhibit c-Fos activity. The role of this pathway was functionally confirmed using T-5224, which reduced acid-induced CRH expression and secretion in ASIC1a-overexpressing primary neurons, lowering secretion levels from 30.18 ng/L to 27.82 ng/L, compared to the control’s 25.85 ng/L (Fig. 5H–K).

Fig. 5: ASIC1a facilitated CRH transcription via Ca2+/CaMKII/c-Fos pathway.
Fig. 5: ASIC1a facilitated CRH transcription via Ca2+/CaMKII/c-Fos pathway.
Full size image

A Acid (pH 6.5)-induced changes in cytosolic Ca2+ signal, indicated by GCaMP6 fluorescence, in cultured mouse hypothalamic neurons (n = 77 in Vector group, n = 63 in OE ASIC1a group, n = 48 in shASIC1a group, n = 73 in OE ASIC1a + PcTx1 group, n = 60 in OE ASIC1a + Amiloride group). B Representative western blot assay showing the expression of calcium signaling pathway-related proteins in primary hypothalamic neurons. Experimental treatments were conducted as in Fig. 4F. C The bar graph illustrates the grayscale scanning analysis of Fig. 5B, showing the relative expression levels of P-CaMKII (n = 3 per group). **p < 0.01 (one-way ANOVA). D The bar graph illustrates the grayscale scanning analysis of Fig. 5B, showing the relative expression levels of c-Fos (n = 3 per group). *p < 0.05 (one-way ANOVA). E The bar graphs show the mRNA expression levels of c-Fos in primary hypothalamic neurons detected by qPCR. Experimental treatments were conducted as in Fig. 4F (n = 3 per group). ****p < 0.0001 (one-way ANOVA). F Representative confocal images (scale bar = 10 μm) of c-Fos and CRH in primary hypothalamic neurons overexpressing GFP/ASIC1-GFP or knockdown of ASIC1a for 48 h, before or 15 min after treatment with HBSS at pH 6.5 with or without 100 nM PcTx1 or 200 nM amiloride. G The bar graph illustrated the relative fluorescence intensity of c-Fos shown in Fig. 5F (n = 3 per group). ****p < 0.0001 (one-way ANOVA). H The bar graph shows the secretion levels of CRH in primary hypothalamic neuron culture supernatants detected by ELISA, after treatment with pH 6.5 HBSS or simultaneous treatment with 80 μM T-5224 for 30 min following 48-h overexpression of ASIC1a (n = 3 per group). *p < 0.05 (one-way ANOVA). I Representative western blot assay showing the protein expression levels of CRH, ASIC1a, and c-Fos in primary hypothalamic neurons. Experimental treatments were conducted as in Fig. 5H. J The bar graph illustrates the grayscale scanning analysis of Fig. 5I, showing the relative expression levels of c-Fos (n = 3 per group). *p < 0.05 (one-way ANOVA). K The bar graph illustrates the grayscale scanning analysis of Fig. 5I, showing the relative expression levels of CRH (n = 3 per group). *p < 0.05 (one-way ANOVA). See also Supplementary Data 2.

In mice, we observed a significant increase in phosphorylated CaMKII protein in the PVN of stressed mice compared to the controls (Supplementary Figure 6A, B). To evaluate whether c-Fos modulates the stress response, T-5224 was bilaterally infused into the PVN through implanted catheters in naïve mice, followed by behavioral assessments. The T-5224 group spent more time in the center of the OFT and in the open arms of the EPM compared to the ACSF group (Supplementary Figure 6C, D) and exhibited significant reduction in immobility time in the TST and FST (Supplementary Figure 6E, F). These findings demonstrated that ASIC1a activation promotes CRH transcription by mediating acid-induced calcium influx, which triggers the CaMKII/c-Fos pathway both in vitro and in vivo and subsequently contributes to anxiety- and depressive-like behaviors.

Discussion

This study identified the presence of ASIC1a specifically in the CRH-producing neurons of the paraventricular nucleus (CRHPVN neurons). Using both pharmacological inhibition of ASIC1a in the PVN and AAV-mediated manipulation of ASIC1a expression in CRHPVN neuron, we delineated a prominent influence of ASIC1a on intracellular Ca2+ concentration and the activity of CRHPVN neuron, thereby regulating plasma ACTH and corticosterone levels. Down-regulating ASIC1a has been shown to mitigate anxiety- and depression-related behaviors in mice. By modulating ASIC1a expression and employing ASIC1a inhibitors, in conjunction with T-5224 to obstruct the AP-1 DNA binding activity, our evidence solidifies the notion that ASIC1a affects CRH transcription via the Ca2+/CaMKII/c-Fos pathway, and activation of ASIC1a promotes CRH release (Fig. 6). Our data indicate that c-Fos is a critical mediator of the acute stress response. While the effects of T-5224 are mediated through AP-1 inhibition, the behavioral and molecular phenotypes we observed are consistent with the blockade of a c-Fos-centric transcriptional program, giving its status as the primary and rapidly inducible component of AP-1 in our model of acute stress.

Fig. 6: Schematic showing ASIC1a promoted the expression of CRH by activating Ca2+/CaMKII/c-Fos signaling pathways.
Fig. 6: Schematic showing ASIC1a promoted the expression of CRH by activating Ca2+/CaMKII/c-Fos signaling pathways.
Full size image

This figure was created by Figdraw (ID: TSRYP14a5b).

The CRHPVN neurons serve as a crucial hub for modulation of HPA axis activity and are viewed as the canonical endocrine controller in the modulation of stress [8]. These neurons receive inputs from many brain regions that convey various homeostatic or stress modes to activate the HPA axis upon stress challenge [7]. Ion channels and receptors determine the activity of the CRHPVN neuron, influencing its role in the modulation of stress. For example, glutamatergic transmission is involved in HPA activation [4]. Notably, CRHPVN neurons have recently been demonstrated to orchestrate stress responses independently of endocrine signals, coordinating complex behaviors through excitatory projections to intra-hypothalamus regions such as lateral hypothalamus [10]. CRHPVN neurons also integrate widespread information from extra-hypothalamus regions including forebrain and midbrain through multiple direct long-range GABAergic afferents to modulate stress [8]. The activity of the CRHPVN neuron, is modulated by diverse excitatory and inhibitory inputs from extra- and intra-hypothalamic brain regions. Therefore, the output of the HPA axis is determined by the integration of these signals to modulate stress response. The innate response to predator odor activates CRH neurons in the PVN through the amygdala-piriform transition area and cortical amygdala, which does not require activation of brainstem noradrenergic neurons [50]. Norepinephrine causes a robust activation of glutamatergic synaptic inputs and a less robust activation of GABAergic synaptic inputs to CRHPVN neurons via a postsynaptic α1 adrenoreceptor-dependent retrograde neuronal-glial signaling mechanism, resulting in a net excitation of CRH neurons [9]. Additionally, amygdala excitation will diminish BNST activity and remove the inhibitory tone constraining CRHPVN activation [51]. Newly identifying ion channels and receptors that influencing the CRHPVN neuron activity will no doubt advance our understanding of molecular mechanisms underlying modulations of HPA axis and mood related behaviors.

Manipulating ASIC1a in the PVN affects mood related behaviors, consistent with previous reports on the important involvement of ASIC1a in the modulation of anxiety- and depression-related behaviors [37]. Coryell et al. has demonstrated that downregulation and inhibition of ASIC1a in the amygdala produce antidepressant-like effects [32]. Pharmacological inhibition and genetic knockdown of ASIC1a in the central nucleus of amygdala has shown to ameliorate anxiety-related behaviors [33]. Moreover, ASIC1a increases inhibitory activity in the basolateral amygdala and decreases anxiety during estrus [34]. Also, a crucial role of ASIC1a in the basolateral amygdala in pain and anxiety-related behaviors during arthritis has been reported that blocking ASIC1a in the basolateral amygdala can both reduce pain as well as anxiety related behaviors associated with arthritis [52]. Additionally, targeting ASIC1a gene or acutely inhibiting ASIC1a suppresses fear and anxiety independent of conditioning [27]. Overexpression of ASIC1a in transgenic mice increases fear conditioning [35]. Restoring ASIC1a expression in the basolateral amygdala rescues the CO2-induced fear deficit in the ASIC1a null mouse [53]. Our recent study has indicated the presence of ASIC1a in the PVN and inhibition of ASICs may act on the HPA axis to alleviate the depression-related behavior in the chronic stress-subjected rat [37]. Mechanically, our data on immunofluorescence staining in this study further localized the expression of ASIC1a in the CRHPVN neuron. Furthermore, we found that downregulation of ASIC1a in the CRHPVN neuron reduced neuronal activity, alongside the decreased HPA axis activity.

At cellular levels, this study revealed a direct relationship between ASIC1a and CRH expression via Ca2+/CaMKII/c-Fos signaling pathway. As an early response gene, CRH is primarily released through de novo synthesis in the PVN in response to stress challenge [54]. The Ca2+ signaling pathway is an integral part of the cellular early response system, capable of being activated within seconds to mins to respond to various stimuli [55]. The ASIC1a-induced alteration in intracellular Ca2+ concentration impacted CRH neuronal activity, leading to a swift upregulation of CRH mRNA levels. Previous study has shown that CRH promoter harbors AP-1 binding sites, responsive to the c-Fos/AP-1 signaling pathway [56]. This aligns with earlier findings that have observed the co-localization and co-activation of c-Fos and CRH in the PVN [57], along with stress-induced alterations in the expression of both c-Fos and CRH in CRHPVN neuron [58]. Following acid stimulation, we noted a concurrent upregulation of p-CaMKII, and c-Fos in primary hypothalamic neurons. Moreover, T-5224, a selective AP-1 DNA binding blocker was employed to inhibit CRH expression. The rapid activation of CRH neurons in vivo (Fig. 3L) likely reflects ASIC1a-mediated depolarization and immediate calcium influx, which facilitate acute stress responses. In contrast, the slower changes in CRH release and expression observed in vitro (Figs. 4 and 5) may represent downstream effects of prolonged ASIC1a activation under sustained acidic conditions. These findings suggest that ASIC1a contributes to distinct roles across different timescales: mediating rapid neuronal activation and regulating longer-term processes. Therefore, this study elucidates a direct molecular mechanism by which ASIC1a modulates HPA axis and mood related behaviors.

Our preceding study has demonstrated that ASIC1a within the PVN participates in modulating glucose metabolism and energy balance [36]. HPA axis is the major neuroendocrine axis that maintains homeostasis in mammals, including glucose metabolism and energy balance [59]. This study reported that ASIC1a in the PVN modulates the HPA axis activity, which further ameliorated anxiety- and depression-related behaviors by modulating CRHPVN neuronal activity. Some drugs that act on known excitatory neurotransmitter-activated receptor, such as NMDA receptor, have been used to prevent the consolidation of fear memory in rodents. However, drug adverse reactions make them less usable. This study on ASIC1a facilitation of CRHPVN neuronal activity suggests that intervention of ASIC1a could normalize HPA axis function with a potentially more favorable side-effect profile, warranting further exploration. Acetazolamide, a non-selective ASIC1a blocker, is known to inhibit fear conditioning, which strongly supports a tonic, physiologically relevant role for ASIC1a in preventing fear memory consolidation, independent of NMDA receptor function [60]. Therefore, this study could provide a new explanation for the drug treatment. ASIC1a has been extensively implicated in regulating synaptic function, neuronal plasticity and complex behaviors such as learning, memory, and fear responses [41, 61,62,63]. Especially, ASIC1a has been proven to contribute to both major forms of synaptic plasticity: long-term potentiation (LTP) and long-term depression (LTD) in different physiological and pathological conditions. For example, in the striatum, ASIC1a enhances excitatory synaptic function, thereby supporting striatum-dependent plasticity as well as procedural learning and memory [20]. The evidence from the hippocampal-prefrontal circuitry study indicates that ASIC1a contributes to extinction-driven plasticity via modulation of NMDA receptor activity [64]. Previous studies have confirmed that ASIC1a is activated by extracellular protons due to synaptic vesicle release during neurotransmission and contributes to excitatory postsynaptic currents [31, 65, 66]. A study by Coryell and work colleagues has revealed that ASIC1a in the amygdala is activated by endogenous pH fluctuations during emotional stress [32]. These studies suggest ASIC1a in the PVN might be activated by local acidification in response to acute stress.

Some limitations should be noted in this study. Firstly, this study mainly focuses on the immediate effects of ASIC1a on acute stress responses, leaving a gap in understanding the role of ASIC1a in long-term stress impacts on stress-related behaviors and diseases. Secondly, despite delving into how ASIC1a facilitates CRH transcription through the Ca2+/CaMKII/c-Fos pathway, other signaling pathways should be existed and are needed to be investigated. Thirdly, we inferred that ASIC1a was activated under stress conditions without direct measurement of in vivo micro-pH dynamics in the PVN. Finally, the study was conducted only in male mice in order to avoid the estrus cycle-induced variation. Further study in female mice should be carried out to explore whether ASIC1a have different physiologies depending on gender.

Collectively, this study presents a novel modulation mechanism of HPA axis and mood behaviors by ASIC1a in the CRHPVN neuron through ASIC1a-mediated intracellular Ca2+ signaling pathway. In the condition of acute stress, increased activity of CRHPVN neuron causes activation of HPA axis activity through ASIC1a-mediated elevated CRH expression that is partly attributed to ASIC1a/Ca2+/CaMKII/c-Fos signaling pathway. Therefore, this study proposes ASIC1a as a potential therapeutic target for stress-related diseases such as depression, anxiety and diabetes.