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

Haruwaka, K.; Liu, J.; Liang, Y.; Matsumoto, S.; Kleidonas, D.; Shi, W.; Zhao, S.; Liu, Y. U.; Umpierre, A. D.; Xie, Z.; Jing, M.; Wu, L.-J.

2026-07-06 neuroscience
10.64898/2026.07.05.735345 bioRxiv
Show 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 Ca2+ 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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