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GABA 受体亚基组成调节视交叉上核中细胞的睡眠-觉醒节律和同步性。

GABA receptor subunit composition regulates circadian rhythms in rest-wake and synchrony among cells in the suprachiasmatic nucleus.

机构信息

Department of Biology, Washington University in St. Louis, MO 63130-4899.

Department of Psychiatry, Washington University in St. Louis, MO 63130-4899.

出版信息

Proc Natl Acad Sci U S A. 2024 Jul 30;121(31):e2400339121. doi: 10.1073/pnas.2400339121. Epub 2024 Jul 24.

DOI:10.1073/pnas.2400339121
PMID:39047036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11295074/
Abstract

The mammalian circadian clock located in the suprachiasmatic nucleus (SCN) produces robust daily rhythms including rest-wake. SCN neurons synthesize and respond to γ-aminobutyric acid (GABA), but its role remains unresolved. We tested the hypothesis that γ2- and δ-subunits of the GABA receptor in the SCN differ in their regulation of synchrony among circadian cells. We used two approaches: 1) shRNA to knock-down (KD) the expression of either γ2 or δ subunits in the SCN or 2) knock-in mice harboring a point mutation in the M2 domains of the endogenous GABA γ2 or δ subunits. KD of either γ2 or δ subunits in the SCN increased daytime running and reduced nocturnal running by reducing their circadian amplitude by a third. Similarly, δ subunit knock-in mice showed decreased circadian amplitude, increased duration of daily activity, and decreased total daily activity. Reduction, or mutation of either γ2 or δ subunits halved the synchrony among, and amplitude of, circadian SCN cells as measured by firing rate or expression of the PERIOD2 protein, in vitro. Surprisingly, overexpression of the γ2 subunit rescued these phenotypes following KD or mutation of the δ subunit, and overexpression of the δ subunit rescued deficiencies due to γ2 subunit KD or mutation. We conclude that γ2 and δ GABA receptor subunits play similar roles in maintaining circadian synchrony in the SCN and amplitude of daily rest-wake rhythms, but that modulation of their relative densities can change the duration and amplitude of daily activities.

摘要

哺乳动物的生物钟位于视交叉上核(SCN),产生包括休息-觉醒在内的强大的每日节律。SCN 神经元合成并响应γ-氨基丁酸(GABA),但其作用仍未解决。我们测试了这样一个假设,即在 SCN 中的 GABA 受体γ2 和 δ 亚基在调节生物钟细胞的同步性方面存在差异。我们使用了两种方法:1)shRNA 敲低(KD)SCN 中的γ2 或 δ 亚基的表达,或 2)携带内源性 GABA γ2 或 δ 亚基 M2 结构域点突变的 knock-in 小鼠。SCN 中γ2 或 δ 亚基的 KD 通过将其昼夜节律振幅降低三分之一,增加了白天的跑步活动,并减少了夜间的跑步活动。同样,δ 亚基 knock-in 小鼠表现出昼夜节律振幅降低、每日活动持续时间增加和总每日活动减少。体外测量的放电率或 PERIOD2 蛋白表达表明,γ2 或 δ 亚基的减少或突变使 SCN 细胞的昼夜节律同步性和振幅减半。令人惊讶的是,在 KD 或 δ 亚基突变后,γ2 亚基的过表达挽救了这些表型,而 δ 亚基的过表达挽救了由于 γ2 亚基 KD 或突变引起的缺陷。我们得出结论,γ2 和 δ GABA 受体亚基在维持 SCN 中的昼夜节律同步性和每日休息-觉醒节律的振幅方面发挥相似的作用,但调节它们的相对密度可以改变每日活动的持续时间和振幅。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/f8a503ac18c9/pnas.2400339121fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/74540e17c2de/pnas.2400339121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/5ff09ade224c/pnas.2400339121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/e59bde98170f/pnas.2400339121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/11fd9110569b/pnas.2400339121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/f8a503ac18c9/pnas.2400339121fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/74540e17c2de/pnas.2400339121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/5ff09ade224c/pnas.2400339121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/e59bde98170f/pnas.2400339121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/11fd9110569b/pnas.2400339121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33a9/11295074/f8a503ac18c9/pnas.2400339121fig06.jpg

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