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Astrocyte-to-microglia purinergic signaling mediates synaptic shielding and promotes neuronal activity

Koichiro HaruwakaiD, Juan LiuiD, Yue LiangiD, Shinya MatsumotoiD, Dimitrios KleidonasiD, Wu Shi, Shunyi ZhaoiD, Yong LiuiD, Anthony D. UmpierreiD, Zhongcong Xie, Miao JingiD, Long‐Jun WuiD

PDFDOI

Abstract

How glial cells sense and regulate neuronal hypoactivity remains poorly understood. Using in vivo imaging in anesthetized, sleeping, and behaving mice, we identified a glial purinergic signaling mechanism that converts neuronal hypoactivity into local circuit regulation. Cortical hypoactivity increased spatially confined ATP release through astrocytic pannexin-1 hemichannels, which were structurally enriched near perisomatic parvalbumin-positive boutons. Local ATP release directed microglial process movement and stabilized bulbous endings through microglial P2Y12 signaling, accompanied by localized Ca{superscript 2} activity in microglial processes. Disruption of astrocytic pannexin-1 or microglial P2Y12 impaired bulbous-ending stabilization and abolished rebound increases in neuronal activity during emergence from anesthesia. Similar ATP release and bulbous-ending formation were observed during chemogenetic neuronal silencing or natural sleep in freely behaving mice. These findings identify astrocyte-to-microglia purinergic signaling as a mechanism that converts neuronal hypoactivity into synapse-selective microglial regulation of circuit activity.

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