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
- Natsuki Shinoda (ORCID: https://orcid.org/0000-0002-6668-8747)
- Yuji Ikegaya (ORCID: https://orcid.org/0000-0003-2260-8191)
- Tasuku Araki (ORCID: https://orcid.org/0000-0002-4904-398X)
- Masayuki Miura (ORCID: https://orcid.org/0000-0001-7444-5705)
- Yusuke Taira (ORCID: https://orcid.org/0000-0002-1106-0266)
- Haruki Takeuchi (ORCID: https://orcid.org/0000-0003-4911-4060)
- Ryuta Koyama (ORCID: https://orcid.org/0000-0001-7108-174X)
- Megumi Andoh
- Yuka Kasahara (ORCID: https://orcid.org/0000-0002-1978-6117)
Institutions
- National Center of Neurology and Psychiatry (JP)
- The University of Tokyo (JP)
- National Institute of Information and Communications Technology (JP)
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
- Japan Agency for Medical Research and Development
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency
- Exploratory Research for Advanced Technology