Nonapoptotic caspase-3 guides C1q-dependent synaptic phagocytosis by microglia

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.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-01-22
DOI
https://doi.org/10.1038/s41467-025-56342-7
Citations
19
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
16.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Nonapoptotic caspase-3 guides C1q-dependent synaptic phagocytosis by microglia

Natsuki Shinoda, Yuji Ikegaya, Tasuku Araki, Masayuki Miura et al.
19 citations
Nature Communications
Neuroinflammation and Neurodegeneration Mechanisms
16.00
article

Nonapoptotic caspase-3 guides C1q-dependent synaptic phagocytosis by microglia

Natsuki Shinoda, Yuji Ikegaya, Tasuku Araki, Masayuki Miura, Yusuke Taira, Haruki Takeuchi, Ryuta Koyama, Megumi Andoh, Yuka Kasahara
article en
19 citations

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.

Nature CommunicationsVol. 16(1)
National Center of Neurology and Psychiatry (JP), The University of Tokyo (JP), National Institute of Information and Communications Technology (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science, Japan Science and Technology Agency, Exploratory Research for Advanced Technology
Openalex Percentile: Top 1%
Neuroinflammation and Neurodegeneration Mechanisms
16.00
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.