Lateral Ventricular Neural Stem Cells (LV NSCs) Regulate Neural Circuitry Activity Through GABAergic Signaling

1. Introduction

The subventricular zone (SVZ) is one of the two principal neurogenic niches in the adult brain [1,2]. In rodents, neurons generated in the SVZ migrate to the olfactory bulb, where they differentiate into granule neurons and periglomerular neurons [3]. Upon integration into the olfactory bulb's local circuitry, these neurons play a key role in olfaction and related behaviors [4].

Neural stem cells (NSCs) can be quiescent or active, and these states are regulated by many factors including synaptic inputs from various brain regions [5,6]. For example, NSCs in the lateral ventricle (LV) are influenced by projections from the hypothalamus and cingulate cortex [7]. Previous work showed that the anterior cingulate cortex (ACC), an area in the frontal cortex, projects to subependymal-neurons expressing choline acetyltransferase (ChAT⁺) bordering the LV, and this ACC-subep-ChAT⁺ circuit modulates the activity of quiescent LV NSCs through the activation of muscarinic M3 receptors [8,9]. M3 activation leads to intracellular calcium release from the endoplasmic reticulum, which initiates a signaling cascade that ultimately promotes proliferation in LV NSCs [9]. This finding raises the question of how LV NSC proliferation may influence the ACC-subep-ChAT⁺ circuit. In particular, can the NSCs produce a negative feedback signal that reduce circuit activation. One possible mechanism for such an influence is through gamma-aminobutyric acid (GABA)-mediated signaling, since subep-ChAT⁺ neurons also express GABA_A receptors [8]. To test hypothesis, we investigated the capacity of LV NSCs in the ventral SVZ to synthesize GABA and regulate its transport.

We first analyzed published RNA sequencing (RNA-seq) data from SVZ LV NSC cultures, including both control and carbachol-treated samples [10]. The RNA-seq data identified high expression levels of monoamine oxidase B (MAOB) in LV NSCs. MAOB, an enzyme predominantly found in astrocytes, catalyzes the breakdown of putrescine to facilitate GABA synthesis [11]. Furthermore, there is significant expression of LRRC8D, the largest isoform in the LRRC8 protein family. LRRC8D functions as a subunit of the volume-regulated anion channels (VRACs) [13], which may play a role in transporting GABA [12,13]. Finally, we also found significant expressions of SLC6A1, the gene encoding the GABA transporter 1 (GAT-1). GAT-1 facilitates the reuptake of extracellular GABA into neurons and glia [14]. These findings suggest a potential functional role for GABA in modulating the ACC-subep-ChAT⁺ circuit, which may in turn influence the activation and proliferation of LV NSCs (Figure 1A).

We found that, in LV NSCs, MAOB expression is increased in response to ACC-subep-ChAT⁺ circuit activation. LRRC8D and SLC6A1 proteins are expressed in both quiescent and activated NSCs within the ventral SVZ. They appear to regulate the impact of ACC-subep-ChAT⁺ circuit stimulation on LV NSC proliferation.

2. Materials and Methods

2.1. Chemicals

The antibodies and compounds used in this study are as follows: BMP-4 Protein (Catalog #: 5020-BP, R&D Systems), Carbachol (Catalog #: 212385-M, Millipore Sigma), Compound 21 (DREADD Agonist 21 dihydrochloride, Catalog #: SML2392, Sigma-Aldrich), DCPIB (Catalog #: 1540, Tocris), and CI966 (Catalog #: 1296, Tocris).

2.2. Mice

All experiments were conducted in compliance with an approved protocol from the Institutional Animal Care and Use Committee at Duke University. Mice were group-housed under a 12-hour light/dark cycle (lights on at 7 a.m.), a controlled ambient temperature of 21°C, and 45% humidity. The following mouse lines were obtained from The Jackson Laboratory (JAX): C57BL/6J (Stock #000664) and Cr-Cre (Stock #010774). Both male and female mice, aged between postnatal day 35 (P35) and postnatal day 65 (P65), were included in the study.

2.3. Viruses

pAAV-hSyn-DIO-hM3D(Gαq)-mCherry was purchased from Addgene (Addgene, #44361).

2.4. Antibodies

The study utilized several primary and secondary antibodies to facilitate experimental investigations. Primary antibodies included Anti-Choline Acetyltransferase Antibody (Catalog #AB144P, Millipore Sigma), Mash1 antibodies from ThermoFisher Scientific (Catalog #14-5794-82) and Abcam (Catalog #ab211327), and EGRF (Catalog #AF231, R&D Systems). Additional primary antibodies used were GFAP Chicken Antibody (Catalog #GFAP, Aves Labs), γ-tubulin Monoclonal Antibody (4D11) (Catalog #MA1-850, ThermoFisher Scientific), GABA Polyclonal Antibody (Catalog #PA5-32241, ThermoFisher Scientific), Monoamine Oxidase B Polyclonal Antibody (Catalog #PA5-18442, ThermoFisher Scientific), LRRC8D Polyclonal Antibody (Catalog #11537-1-AP, Proteintech), and SLC6A1 Polyclonal Antibody (Catalog #PA5-85766, ThermoFisher Scientific).

For secondary antibodies, we used Alexa Fluor® 488 AffiniPure™ Donkey Anti-Rabbit IgG (H+L) (Catalog #711-545-152, Jackson ImmunoResearch) and Alexa Fluor® 594 AffiniPure™ Donkey Anti-Rabbit IgG (H+L) (Catalog #711-585-152, Jackson ImmunoResearch). Additional reagents included Alexa Fluor® 594 AffiniPure™ Donkey Anti-Goat IgG (H+L) (Catalog #705-585-003, Jackson ImmunoResearch), Alexa Fluor® 647 AffiniPure™ Donkey Anti-Goat IgG (H+L) (Catalog #705-605-147, Jackson ImmunoResearch), and Alexa Fluor® 488 AffiniPure™ Donkey Anti-Mouse IgG (H+L) (Catalog #715-545-150, Jackson ImmunoResearch). Secondary antibodies targeting chicken IgY (IgG) included Alexa Fluor® 488 AffiniPure™ Donkey Anti-Chicken IgY (H+L) (Catalog #703-545-155, Jackson ImmunoResearch) and Alexa Fluor® 647 AffiniPure™ Donkey Anti-Chicken IgY (H+L) (Catalog #703-605-155, Jackson ImmunoResearch). Finally, Alexa Fluor® 647 AffiniPure™ Donkey Anti-Mouse IgG (H+L) (Catalog #715-605-151, Jackson ImmunoResearch) was also utilized.

2.5. Stereotaxic Injections

Stereotaxic injections were conducted on deeply anesthetized mice secured in a stereotaxic frame (David Kopf Instruments) under isoflurane anesthesia. For in vivo chemogenetic activation of the ACC-subep-ChAT⁺ circuit, 300 nl of the viral vector pAAV-hSyn-DIO-hM3D(Gαq)-mCherry was injected into the ACC region of Cr-Cre (P30) mice. The injection was performed at the following coordinates relative to Bregma: anterior-posterior (AP) +0.8 mm, mediolateral (ML) ± 0.25 mm, dorsoventral (DV) −0.3 mm from the brain surface. Viral infusion was performed slowly for over 10 minutes using a Nanoject injector (Drummond Scientific) connected to a glass pipette. To ensure optimal viral distribution, the pipette was left in place for an additional 10-minute post-injection before being retracted.

Local inhibition of LRRC8D and SLC6A1 was achieved using DCPIB and CI966, respectively, using a micro-osmotic pump (Model 1003D, Alzet) for drug delivery. During the same surgical session, a cannula was implanted into the LV of Cr-Cre (P30) mice at the following coordinates: AP +0.8 mm, ML ± 0.65 mm, DV −2.1 mm from the brain surface. 300 nl of the pAAV-hSyn-DIO-hM3D(Gαq)-mCherry virus was injected into the ACC as previously described.

Cortical circuit activation was achieved via intraperitoneal administration of DREADD agonist C21 10 hours after connecting the osmotic pump, which facilitated drug perfusion. The osmotic pump delivered the drugs at a flow rate of 1 µl per hour for a duration of 12 hours, following the manufacturer's instructions. Experimental timelines and results are presented in Figures 5 and 7.

2.6. Immunofluorescence Staining and Imaging

Brain tissues were prepared for immunohistochemical (IHC) staining to investigate subep-ChAT+ neurons and cortical circuit modulations in chemogenetic in vivo experiments. At the conclusion of the experiments, mice were deeply anesthetized with isoflurane and transcardially perfused with phosphate-buffered saline (PBS), followed by 4% paraformaldehyde (PFA) in PBS. The brains were then carefully removed and post-fixed in 4% PFA at 4°C overnight.

For SVZ whole-mount preparations, the dissected tissues were incubated in a blocking solution consisting of 5% donkey serum and TBST for 100 minutes at room temperature. Subsequently, they were incubated overnight at room temperature in PBS containing 1% donkey serum and specific primary antibodies validated either in our prior publication [8] or in vendor-provided references. Following primary antibody incubation, the tissues were washed in PBS and then treated with secondary antibodies, including Alexa-594 (1:1000, Life Technologies), Alexa-488 (1:1000, Life Technologies), or Alexa-647 (1:1000, Life Technologies), for two hours at room temperature. Afterward, the tissues were washed in PBS and counterstained with 4',6-diamidino-2-phenylindole (DAPI; Sigma-Aldrich). Finally, the samples were washed four times with TBST and mounted on slides using Fluoromount (Sigma), an aqueous mounting medium

Images were acquired using a Leica SP8 upright confocal microscope (Zeiss) equipped with 10×, 40×, and 63× objectives and controlled via Zen software (Zeiss). To visualize the ventricular-SVZ (V-SVZ) region within the SVZ niche, tile-scan imaging was used, and confocal stacks of 1.5 to 3 μm optical sections were captured to illustrate the monolayer of cells just beneath the ependymal layer. The V-SVZ layer is labeled in the images presented in this manuscript. Additionally, wider-field images encompassing both the ventral SVZ and SVZ regions were acquired using confocal stacks ranging from 8 to 11 μm in depth. These images depict the spatial arrangement of subep-ChAT+ neurons within the SVZ and the layer of LV NSCs, including quiescent LV NSCs, located beneath the ependymal layer in the V-SVZ region.

2.7. In Vivo Stimulation of Chemogenetic Circuits and Local Protein Inhibition in the SVZ

Following stereotaxic viral infusion as detailed in the "Stereotaxic Injections" section and the experimental design illustrated in Fig. 2A, C21 was prepared by dissolving in 0.9% saline and stored at -20°C until use. Intraperitoneal injections of C21 were administered at a dosage of 1 mg/kg. Chemogenetic circuit stimulation in vivo was initiated by intraperitoneal C21 injection, delivered 6 hours prior to the experiment's conclusion.

Simultaneous assessments of in vivo chemogenetic circuit stimulation and localized inhibition of LRCC8D and SLC6A1 proteins in the LVs were conducted (Figs. 5A, 5B, 7A, and 7B). In these experiments, the ventral SVZ was exposed to localized protein inhibition using DCPIB (5 µM) and CI966 (1.5 µM) via continuous infusion for 12 hours. Circuit activation was then initiated during the final 10 hours before the conclusion of the experiment.

For downstream analyses, SVZ wholemounts were dissected to examine the expressions of Mash1, GABA, MAOB, LRRC8D, and SLC6A1. Quantitative comparisons were made between the ipsilateral sides (receiving circuit activation or combined circuit activation and local protein inhibition) and the contralateral control sides. Specifically, the number of GABA⁺ Mash1⁺ NSCs/GABA⁺ NSCs, MAOB⁺ Mash1⁺ NSCs/MAOB⁺ NSCs, LRRC8D⁺ Mash1⁺ NSCs/LRRC8D⁺ NSCs, and SLC6A1⁺ Mash1⁺ NSCs/SLC6A1⁺ NSCs surrounding subep-ChAT⁺ neurons were analyzed. These comparisons provided insights into the spatial and functional effects of chemogenetic stimulation and protein inhibition on neural stem cell populations.

2.8. SVZ NSC Culture

SVZ NSC cultures were derived from SVZ wholemounts obtained from postnatal (P12) C57BL/6J mice as described previously [9]. The dissected tissues were placed in DMEM/F-12 (DF) medium supplemented with 100 units/ml penicillin, 100 μg/ml streptomycin, and 250 ng/ml amphotericin B (abx). Following dissection, the pooled tissues were incubated in 0.005% trypsin at 37°C (pH 7.3) for 15 minutes.

After enzymatic digestion, the tissues were transferred to uncoated T75 plastic tissue-culture dishes and incubated overnight in N5 medium. The N5 medium consisted of DF supplemented with N2 supplements, 35 μg/ml bovine pituitary extract, abx, 5% fetal calf serum (FCS, HyClone), and 40 ng/ml each of epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF). Unattached cells were collected, replated on uncoated plastic dishes, and cultured in N5 medium until they reached 90–100% confluency. The medium was refreshed every other day for 3–4 days during proliferation.

Freshly cultured cells were exclusively utilized for all experiments. To induce quiescence in LV NSCs, cells were exposed to 10 ng/ml BMP4 for 24 hours. Following quiescence induction, cells were treated under one of three conditions for an additional 24 hours: media only (control), media supplemented with carbachol (15 µM), or media containing carbachol (15 µM) combined with a selective protein inhibitor. At the conclusion of the treatment period, experiments were terminated by fixing the cells in 4% PFA. Subsequent immunostaining was performed to analyze and quantify cellular responses.

2.9. Quantification and Statistical Analysis

Statistical analyses were performed using GraphPad Prism software (version 8). Paired t-tests were used for both in vivo chemogenetic stimulation studies and in vitro SVZ NSC culture modulation experiments.

To quantify the proportions of GABA⁺-Mash1⁺ NSCs/GABA⁺ NSCs, MAOB⁺-Mash1⁺ NSCs/MAOB⁺ NSCs, LRCC8D⁺-Mash1⁺ NSCs/Mash1⁺ NSCs, and SLC6A1⁺-Mash1⁺ NSCs/SLC6A1⁺ NSCs, as well as the average intensities of GABA per GABA⁺ NSC, MAOB per MAOB⁺ NSC, and SLC6A1 per SLC6A1⁺ NSC in the V-SVZ, 50 μm × 50 μm square images were captured. Each image was centered on a subep-ChAT⁺ neuron to facilitate the analysis of NSC proliferation activity surrounding these neurons.

Biological replicates included five mice per experiment (N = 5), as specified in the figure legends. Paired t-tests were performed to compare the ipsilateral and contralateral sides of the brain within the same animal. The mean number of stained NSCs was calculated from five subep-ChAT⁺ neurons on both the ipsilateral and contralateral sides for each mouse.

Additionally, the quantification of SLC6A1⁺-EGFR⁺ NSCs, as well as the average intensities of GABA per EGFR⁺ NSC and SLC6A1 per EGFR⁺ NSC, was conducted using data from four independent SVZ NSC culture experiments (N = 4), as detailed in Figures 2 and 7. For each experiment, 2–3 wells were analyzed, and paired t-tests were used to assess statistical significance.

3. Results

3.1. Expression and Regulation of GABA Activity in LV NSCs by the ACC-Subep-ChAT⁺ Circuit Activation and Cholinergic Stimulation

Based on RNA-seq data, we hypothesized that LV NSCs possess molecular machinery for synthesizing GABA via MOAB and regulating its transport through LRRC8D and GAT-1. First, we measured GABA expression in brain tissues from P40 C57BL/6J mice. Coronal brain sections were immunostained for GABA, glial fibrillary acidic protein (GFAP), and γ-tubulin to investigate the ventral SVZ domain. GFAP was used as a marker for both quiescent and active LV NSCs, while γ-tubulin specifically identified quiescent NSCs. We found that GFAP⁺-γ-tubulin⁺ cells, corresponding to quiescent LV NSCs, were also positive for GABA, confirming GABA expression in these cells (Figure 1B). We also confirmed that quiescent LV NSCs near subep-ChAT⁺ neurons in the ventral SVZ. were GABA⁺ and γ-tubulin⁺ (Figure 1C). In whole-mount preparations from P35 C57BL/6J mice, GFAP⁺ LV NSCs in the ventral SVZ domain were also GABA⁺, confirming GABA expression in LV NSCs in proximity to subep-ChAT⁺ neurons (Figure 1D).

To examine circuit modulation of GABA activity in LV NSCs, we used chemogenetics to activate the ACC-subep-ChAT⁺ circuit. We injected the pAAV-hSyn-DIO-hM3D(Gαq)-mCherry virus into the ACC of CR-Cre mice (Figure 2A). We activated this circuit using the DREADD agonist for 10 hours, which was sufficient to increase proliferation of LV NSCs in the ventral SVZ near subep-ChAT⁺ neurons. Whole-mount dissections from both hemispheres were stained for GABA, ChAT, and Mash1 (labels activated LV NSCs) (Figure 2B). We found more GABA⁺-Mash1⁺ NSCs on the ipsilateral (circuit activation) side compared to the contralateral (control) side (Figure 2C). Moreover, the intensity of GABA⁺ staining in cells near subep-ChAT⁺ neurons was significantly increased on the ipsilateral side (Figure 2D), demonstrating that the ACC-subep-ChAT⁺ circuit increases GABA in LV NSCs.

To further investigate how cholinergic signaling affects GABA in LV NSCs, in vitro experiments were conducted using cultured SVZ NSCs. Carbachol, a cholinergic agonist, was applied to half of the samples, with cells maintained in a quiescent state as described in Methods. After 24 hours, both control and carbachol-treated samples were stained for GABA, epidermal growth factor receptor (EGFR), and DAPI to evaluate GABA modulation (Figure 2E). The results demonstrated that carbachol treatment increased GABA intensity in EGFR⁺ NSCs compared to controls (Figure 2F). LV NSCs within the ventral SVZ domain express GABA, especially in cells located near subep-ChAT⁺ neurons. The ACC-subep-ChAT⁺ circuit plays a significant role in modulating GABA activity in these cells.

3.2. Expression of MAOB in LV NSCs is modulated by ACC-Subep-ChAT⁺ Circuit Activation

In coronal brain sections from P40 C57BL/6J mice, we found that GFAP⁺-γ-tubulin⁺ NSCs in the ventral ventricular-subventricular zone (V-SVZ) also expressed MAOB (Figure 3A). Moreover, γ-tubulin⁺ NSCs in this area, found next to subep-ChAT⁺ neurons, were likewise positive for MAOB (Figure 3B). In wholemount preparations of the SVZ from P35 C57BL/6J mice, we also found that GFAP⁺ NSCs in the ventral SVZ co-expressed GABA and MAOB (Figure 3C & D).

We then examined the modulation of MAOB protein expression in NSCs by the ACC-subep-ChAT⁺ circuit using a similar chemogenetic activation procedure as described above. SVZ wholemounts from both hemispheres (circuit activation and control) were stained for MAOB, ChAT, and Mash1. Circuit activation increased the number of MAOB⁺-Mash1⁺ NSCs (Figure 3E & F). Additionally, the intensity of MAOB protein in MAOB⁺ cells was markedly higher on the activated side compared to the control (Figure 3G). These findings show that MAOB is expressed in quiescent LV NSCs within the ventral SVZ and can be modulated by the activity of the ACC-subep-ChAT⁺ circuit.

3.3. LRRC8D Expression in LV NSCs and Its Functional Role in ACC-subep-ChAT⁺ Circuit-Modulated Proliferation

RNA-seq data from SVZ NSC cultures showed increased expression of the LRRC8D gene in LV NSCs [10]. LRRC8D encodes a GABA transporter into the extracellular neuronal space. We examined LRRC8D expression in LV NSCs by performing immunofluorescence staining on wholemount preparations from P40 C57BL/6J mouse brains. GFAP⁺-γ-tubulin⁺ NSCs were LRRC8D⁺ (Figure 4A). This finding was also confirmed in coronal brain sections of P40 C57BL/6J mice (Figure 4B). Using wholemounts from P35 C57BL/6J mice, we showed that GFAP⁺ NSCs, located in the ventral V-SVZ near subep-ChAT⁺ neurons, also expressed LRRC8D (Figure 4C).

To evaluate the functional role of LRRC8D in NSCs, we investigated its modulation by the activation of ACC-subep-ChAT⁺ circuit. Wholemounts of the ventral SVZ from both circuit-activated and control sides were stained for LRRC8D, ChAT, and Mash1 (Figure 4D). We found that circuit activation significantly increased the number of LRRC8D⁺-Mash1⁺ NSCs (Figure 4E).

Next, we assessed the impact of LRRC8D inhibition on this circuit-mediated modulation. We compared circuit-activated conditions with and without DCPIB, a selective LRRC8D inhibitor. CR-Cre mice were injected with pAAV-hSyn-DIO-hM3D(Gq)-mCherry virus into the ACC region, and a cannula was implanted to locally infuse DCPIB (5 µM) into the lateral ventricle (Figure 5A). Following the experiment, V-SVZ wholemounts were stained for LRRC8D, ChAT, and Mash1 (Figure B). We found a reduced number of LRRC8D⁺-Mash1⁺ NSCs on the circuit activation + DCPIB infusion side compared to the circuit activation only side (Figure 5C). These findings underscore the critical role of LRRC8D in regulating the activity of the ACC-subep-ChAT⁺ circuit and its impact on the proliferation of LV NSCs in the ventral SVZ.

3.4. SLC6A1 Expression and Its Role in Modulating ACC-subep-ChAT+ Circuit Activity on LV NSCs in the Ventral SVZ

RNA sequencing data from SVZ NSC cultures shows moderate expression of the SLC6A1 gene [10]. SLC6A1 encodes GAT-1, which is essential for the reuptake of GABA. In coronal brain sections from P40 C57BL/6J mice, we found that quiescent GFAP⁺ and γ-tubulin⁺ NSCs in the ventral V-SVZ express SLC6A1 (Figure 6A). Similarly, in P45 mouse brain sections, γ-tubulin⁺ NSCs adjacent to subep-ChAT⁺ neurons also express SLC6A1 (Figure 6B). In SVZ wholemounts from P35 mice, GFAP⁺ NSCs surrounding subep-ChAT+ neurons in the ventral V-SVZ also express SLC6A1 (Figure 6C). In addition, ACC-subep-ChAT⁺ circuit activation increased the number of SLC6A1⁺ Mash1⁺ NSCs (Figure 6D, 5E). However, SLC6A1 intensity within SLC6A1⁺ cells was not affected (Figure 6F).

In SVZ NSC cultures, carbachol-treated NSCs showed higher SLC6A1 intensity, especially in the processes (Figure 6G, 5H). This finding suggests that cholinergic signaling increases SLC6A1 in LV NSCs.

To assess how GAT-1 may modulate the effect of ACC-subep-ChAT⁺ circuit activation on LV NSC proliferation, we used chemogenetic activation as described above. On the ipsilateral side, GAT-1 activity was selectively inhibited using CI966 (1.5 µM) locally infused into the ventral SVZ (Figure 7A). Immunostaining for SLC6A1 (GAT-1), ChAT, and Mash1 revealed that SLC6A inhibition reduced the numbers of SLC6A1+-Mash1⁺ NSCs (Figure 7B & C). Additionally, SLC6A1 intensity was also reduced on the CI966-treated side (Figure 7D).

Finally, cultures treated with both carbachol and CI966 exhibited a reduction in SLC6A1⁺ EGFR⁺ NSCs and lower SLC6A1 intensity compared to carbachol-only treated cultures (Figure 7E, F & G). Thus GAT-1 inhibition reduced the effect of cholinergic signaling on NSC proliferation. These results suggest that GAT-1 may also play a role in regulating ACC-subep-ChAT⁺ circuit-induced proliferation of LV NSCs within the ventral SVZ domain.

4. Discussion

Our previous work showed that the ACC-subep-ChAT⁺ circuit can activate quiescent NSCs and promote proliferation via cholinergic signaling [9]. In this study, we investigated whether LV NSCs can also send a negative feedback signal to regulate ACC-subep-ChAT⁺ circuit and in turn affect proliferation of LV NSCs surrounding subep-ChAT⁺ neurons. Previous work showed that subep-ChAT⁺ neuron activity is inhibited by GABAergic signaling [8]. Here we examined the role of GABA signaling in this network.

Our findings suggest that LV NSCs surrounding subep-ChAT⁺ neurons can produce and potentially release GABA (Figure 1). Since these GABA-producing LV NSCs is influenced by the ACC-subep-ChAT⁺ circuit, GABA may play a role in regulating the subep-ChAT+ neurons and NSC activity, in response to circuit activation and cholinergic signaling (Figure 2).

We investigated the potential of LV NSCs to synthesize GABA by examining whether MAOB, which is highly expressed in both quiescent and active states of LV NSCs, plays a role in GABA production. Our experiments demonstrated that the ACC-subep-ChAT⁺ circuit modulates the activity of the MAOB protein in LV NSCs adjacent to subep-ChAT⁺ neurons, suggesting a role linked to this circuit's activity (Figure 3). Previous studies have identified the putrescine degradation pathway as a biosynthetic mechanism for GABA in astrocytes, with MAOB acting as a key enzyme in this process [11,15]. Given the glia-like properties of LV NSCs, it is possible that they also use similar mechanisms to produce GABA.

In addition, we also examined whether LV NSCs in the ventral SVZ domain express GABA-specific transporters capable of facilitating the extracellular transport of GABA. RNA-seq analysis of SVZ NSCs under carbachol treatment versus control conditions identified high expression of several LRRC8 subunits: Lrrc8d, Lrrc8a, Lrrc8c, and Lrrc8b. Of these, Lrrc8d level was reduced by carbachol treatment [10]. LRRC8 subunits are components of VRACs, which are heteromers facilitating the transport of various neurotransmitters, including glutamate and GABA [13]. LRRC8D mediates the transport of a broad range of organic compounds [16]. Our in vivo findings demonstrate that LV NSCs express the LRRC8D protein (Figure 4). Selective inhibition of LRRC8D within the ventral SVZ resulted in a significant decrease in LV NSC proliferation driven by the activity of the ACC-subep-ChAT⁺ circuit (Figure 5).

We also investigated the capacity of LV NSCs to reuptake GABA from the extracellular space. RNA-seq analysis of SVZ NSCs revealed that both quiescent and active NSCs express the Slc6a1 gene [10], which encodes GAT-1, a key transporter for GABA in the brain. Dysfunction or mutations in SLC6A1 have been linked to neurodevelopmental disorders, in which disrupted GABAergic signaling is associated with developmental delays, epilepsy, autism spectrum disorders, and motor dysfunction [17].

We found that LV NSCs next to subep-ChAT⁺ neurons express SLC6A1 (GAT-1), which transports GABA from the extracellular to intracellular space. Inhibiting GAT-1 is therefore expected to increase GABA signaling in the extracellular space. Indeed, we found that pharmacological inhibition of GAT-1 with CI966 significantly reduced the impact of the ACC-subep-ChAT⁺ circuit on LV NSC proliferation. This finding demonstrates the functional significance of GABA transport in negative feedback signaling.

By demonstrating the direct role of LV NSCs in modulating subep-ChAT⁺ activity and the reciprocal influence of the ACC-subep-ChAT⁺ circuit on LV NSC function, our study highlights the importance of GABAergic signaling in maintaining the balance between neural circuit activity and stem cell proliferation in the ventral SVZ. Our results show a potential role of GABAergic signaling from NSCs as a negative feedback signal to regulate circuit activation stem cell dynamics within the ventral SVZ (Figure 8).

5. Conclusions

By demonstrating the direct role of LV NSCs in modulating subep-ChAT⁺ activity and the reciprocal influence of the ACC-subep-ChAT⁺ circuit on LV NSC function, our study highlights the importance of GABAergic signaling in maintaining the balance between neural circuit activity and stem cell proliferation in the ventral SVZ. Our results show a potential role of GABAergic signaling from NSCs as a negative feedback signal to regulate circuit activation stem cell dynamics within the ventral SVZ (Figure 8). Further research is needed to unravel the precise molecular mechanisms and broader implications of these processes in neurodevelopmental and neurodegenerative disorders.