有节奏的星形细胞GABA的产生与视交叉上核的神经元昼夜节律同步。

IF 9.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
EMBO Journal Pub Date : 2025-01-01 Epub Date: 2024-12-02 DOI:10.1038/s44318-024-00324-w
Natalie Ness, Sandra Díaz-Clavero, Marieke M B Hoekstra, Marco Brancaccio
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引用次数: 0

摘要

哺乳动物视交叉上核(SCN)星形胶质细胞可调节睡眠-觉醒周期。然而,星形胶质细胞提供的控制行为昼夜模式的信息的性质尚不清楚。整个SCN的神经元昼夜活动被组织成时空波,控制季节性适应和及时参与行为输出。在这里,我们发现小鼠SCN中的星形胶质细胞表现出高度均匀的脉冲状夜间活动。我们发现,星形胶质细胞通过多胺降解产生有节奏的GABA提供了SCN电路同步所需的抑制性夜间音调,从而充当星形胶质细胞内部授时子(或“星形胶质授时子”)。我们进一步确定突触GABA和星形细胞GABA是支撑SCN神经元活动连贯时空昼夜节律模式的两个关键参与者。通过描述星形胶质细胞促进昼夜节律的新机制,我们的工作为理解星形胶质细胞如何编码哺乳动物复杂行为背后的时间信息提供了一个总体蓝图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rhythmic astrocytic GABA production synchronizes neuronal circadian timekeeping in the suprachiasmatic nucleus.

Astrocytes of the suprachiasmatic nucleus (SCN) can regulate sleep-wake cycles in mammals. However, the nature of the information provided by astrocytes to control circadian patterns of behavior is unclear. Neuronal circadian activity across the SCN is organized into spatiotemporal waves that govern seasonal adaptations and timely engagement of behavioral outputs. Here, we show that astrocytes across the mouse SCN exhibit instead a highly uniform, pulse-like nighttime activity. We find that rhythmic astrocytic GABA production via polyamine degradation provides an inhibitory nighttime tone required for SCN circuit synchrony, thereby acting as an internal astrocyte zeitgeber (or "astrozeit"). We further identify synaptic GABA and astrocytic GABA as two key players underpinning coherent spatiotemporal circadian patterns of SCN neuronal activity. In describing a new mechanism by which astrocytes contribute to circadian timekeeping, our work provides a general blueprint for understanding how astrocytes encode temporal information underlying complex behaviors in mammals.

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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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