Nonapoptotic Caspase-3 Guides C1q-dependent Synaptic Phagocytosis by Microglia

Overview

Journal Nat Commun

Date 2025 Jan 22

PMID 39843445

Authors

Megumi Andoh

Natsuki Shinoda

Yusuke Taira

Tasuku Araki

Yuka Kasahara

Haruki Takeuchi

Masayuki Miura

Yuji Ikegaya

Ryuta Koyama

Affiliations

Soon will be listed here.

Abstract

Caspases are known to mediate neuronal apoptosis during brain development. However, here we show that nonapoptotic activation of caspase-3 at presynapses drives microglial synaptic phagocytosis. Real-time observation and spatiotemporal manipulation of synaptic caspase-3 in the newly established, mouse-derived culture system demonstrate that increased neuronal activity triggers localized presynaptic caspase-3 activation, facilitating synaptic tagging by complements. High-resolution live imaging reveals that caspase-3 activation promotes synapse-selective complement-dependent microglial phagocytosis without axonal shearing. Furthermore, activity-dependent caspase-3 activation at inhibitory presynapses induces microglial phagocytosis in mice and increases seizure susceptibility. This increased susceptibility is reversed by genetic depletion of microglial complement receptors. Thus, localized, nonapoptotic caspase activity guides complement-dependent microglial synaptic phagocytosis and remodels neuronal circuits.

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