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小胶质细胞通过补体依赖性突触消除来介导遗忘。

Microglia mediate forgetting via complement-dependent synaptic elimination.

机构信息

Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital, NHC and CAMS Key Laboratory of Medical Neurobiology, Zhejiang University School of Medicine, Hangzhou 310058, China.

Center for Stem Cell and Regenerative Medicine, Zhejiang University School of Medicine, Hangzhou 310058, China.

出版信息

Science. 2020 Feb 7;367(6478):688-694. doi: 10.1126/science.aaz2288.

Abstract

Synapses between engram cells are believed to be substrates for memory storage, and the weakening or loss of these synapses leads to the forgetting of related memories. We found engulfment of synaptic components by microglia in the hippocampi of healthy adult mice. Depletion of microglia or inhibition of microglial phagocytosis prevented forgetting and the dissociation of engram cells. By introducing CD55 to inhibit complement pathways, specifically in engram cells, we further demonstrated that microglia regulated forgetting in a complement- and activity-dependent manner. Additionally, microglia were involved in both neurogenesis-related and neurogenesis-unrelated memory degradation. Together, our findings revealed complement-dependent synapse elimination by microglia as a mechanism underlying the forgetting of remote memories.

摘要

记忆痕迹细胞之间的突触被认为是记忆储存的基础,这些突触的减弱或丢失导致相关记忆的遗忘。我们发现健康成年小鼠海马体中的小胶质细胞吞噬了突触成分。小胶质细胞耗竭或抑制小胶质细胞吞噬作用可防止遗忘和记忆痕迹细胞的分离。通过引入 CD55 抑制补体途径,特别是在记忆痕迹细胞中,我们进一步证明小胶质细胞以补体和活性依赖的方式调节遗忘。此外,小胶质细胞参与了与神经发生相关和与神经发生无关的记忆降解。总之,我们的研究结果揭示了小胶质细胞通过补体依赖性突触消除作为遗忘远程记忆的机制。

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