睡眠机制知识库

小胶质细胞经腺苷 A3 受体信号稳定睡眠稳态

Microglia stabilize sleep homeostasis via adenosine A3 receptor signaling.

原始研究开放获取
作者
Zhao Z, Gu X, Yu J, Chen X, Zhang L, Zhao T, Ye W, Cheng H 等
期刊
Science advances
出处
2026; 12(37); eaef3957
DOI
10.1126/sciadv.aef3957
PMID
42726883

一句话摘要

(正式发表版)证明小胶质细胞经腺苷 A3 受体感知脑状态依赖的胞外腺苷波动,其钙活动随脑状态转换快速改变,小胶质细胞特异性缺失 A3 受体则睡眠稳态受损;缺失后形态可塑性受损、觉醒—NREM 转换增多,导致睡眠碎片化。

为什么重要

在同行评审版本中确认了小胶质细胞作为睡眠压力感受器的新角色,把腺苷稳态假说的细胞载体从神经元扩展到胶质细胞。与 P104-P106 所属的涟漪研究无直接关系,但与本条同源条目 P102 需合并阅读。

英文摘要原文

Sleep homeostasis maintains the sleep-wake balance through sleep pressure, a process partly orchestrated by the accumulation of extracellular adenosine (eADO). Microglial Ca 2+ activity has been implicated in sleep regulation, but the mechanism whereby microglia sense sleep pressure remains unclear. Here, we show that microglia regulate sleep homeostasis through brain state-dependent calcium ion activity driven by adenosine A 3 receptor (A 3 R) signaling. Using miniaturized two-photon microscopy in freely behaving mice, we demonstrate that microglial calcium ion activity is rapidly altered by brain-state transitions. Pharmacological experiments reveal that microglial calcium ion dynamics are predominantly mediated by A 3 R in response to brain state-dependent eADO oscillations. Microglia-specific deletion of A 3 R attenuates these state-dependent calcium ion dynamics, impairs microglial morphological plasticity across sleep-wake cycles, and leads to sleep fragmentation by increasing transitions between wakefulness and non-rapid eye movement (NREM) sleep. Together, these findings establish that microglia contribute to sleep homeostasis by stabilizing both wakefulness and NREM sleep, a process partly involving eADO-A 3 R signaling.

所属章节

睡眠稳态与腺苷、双过程模型

腺苷 A3 受体 小胶质细胞 睡眠稳态

条目编号 P103 · 元数据经 Crossref / Europe PMC 回查