期刊
CELL REPORTS
卷 34, 期 12, 页码 -出版社
CELL PRESS
DOI: 10.1016/j.celrep.2021.108899
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资金
- NIH/NINDS
Shisa7 plays a critical role in regulating tonic inhibition in hippocampal neurons by influencing alpha 5-GABA(A)R exocytosis, which requires the involvement of PKA and is essential for activity-dependent regulation and oscillations during the sleep/wake cycle.
Tonic inhibition mediated by extrasynaptic gamma-aminobutyric acid type A receptors (GABA(A)Rs) critically regulates neuronal excitability and brain function. However, the mechanisms regulating tonic inhibition remain poorly understood. Here, we report that Shisa7 is critical for tonic inhibition regulation in hippocampal neurons. In juvenile Shisa7 knockout (KO) mice, alpha 5-GABA(A)R-mediated tonic currents are significantly reduced. Mechanistically, Shisa7 is crucial for alpha 5-GABA(A)R exocytosis. Additionally, Shisa7 regulation of tonic inhibition requires protein kinase A (PKA) that phosphorylates Shisa7 serine 405 (S405). Importantly, tonic inhibition undergoes activity-dependent regulation, and Shisa7 is required for homeostatic potentiation of tonic inhibition. Interestingly, in young adult Shisa7 KOs, basal tonic inhibition in hippocampal neurons is unaltered, largely due to the diminished alpha 5-GABA(A)R component of tonic inhibition. However, at this stage, tonic inhibition oscillates during the daily sleep/wake cycle, a process requiring Shisa7. Together, these data demonstrate that intricate signaling mechanisms regulate tonic inhibition at different developmental stages and reveal a molecular link between sleep and tonic inhibition.
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