加巴能
神经科学
葛根素
中间神经元
神经传递
生物
突触
鸟嘌呤核苷酸交换因子
海马结构
细胞生物学
化学
抑制性突触后电位
信号转导
受体
生物化学
氨基酸
甘氨酸
甘氨酸受体
作者
Seungjoon Kim,Dongseok Park,Jinhu Kim,Dong-Wook Kim,Hyeonho Kim,Takuma Mori,Hyeji Jung,Dongsu Lee,Soon-Jo Hong,Jongcheol Jeon,Katsuhiko Tabuchi,Eunji Cheong,Jaehoon Kim,Ji Won Um,Jaewon Ko
出处
期刊:Cell Reports
[Elsevier]
日期:2021-07-01
卷期号:36 (3): 109417-109417
被引量:11
标识
DOI:10.1016/j.celrep.2021.109417
摘要
Summary
Activity-dependent GABAergic synapse plasticity is important for normal brain functions, but the underlying molecular mechanisms remain incompletely understood. Here, we show that Npas4 (neuronal PAS-domain protein 4) transcriptionally regulates the expression of IQSEC3, a GABAergic synapse-specific guanine nucleotide-exchange factor for ADP-ribosylation factor (ARF-GEF) that directly interacts with gephyrin. Neuronal activation by an enriched environment induces Npas4-mediated upregulation of IQSEC3 protein specifically in CA1 stratum oriens layer somatostatin (SST)-expressing GABAergic interneurons. SST+ interneuron-specific knockout (KO) of Npas4 compromises synaptic transmission in these GABAergic interneurons, increases neuronal activity in CA1 pyramidal neurons, and reduces anxiety behavior, all of which are normalized by the expression of wild-type IQSEC3, but not a dominant-negative ARF-GEF-inactive mutant, in SST+ interneurons of Npas4-KO mice. Our results suggest that IQSEC3 is a key GABAergic synapse component that is directed by Npas4 and ARF activity, specifically in SST+ interneurons, to orchestrate excitation-to-inhibition balance and control anxiety-like behavior.
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