Astrocytes phagocytose adult hippocampal synapses for circuit homeostasis

被引:229
作者
Lee, Joon-Hyuk [1 ]
Kim, Ji-young [2 ,3 ]
Noh, Seulgi [3 ,4 ]
Lee, Hyoeun [2 ]
Lee, Se Young [1 ]
Mun, Ji Young [4 ]
Park, Hyungju [2 ,3 ]
Chung, Won-Suk [1 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Biol Sci, Daejeon, South Korea
[2] Korea Brain Res Inst KBRI, Res Grp Neurovasc Unit, Daegu, South Korea
[3] Daegu Gyeongbuk Inst Sci & Technol DGIST, Dept Brain & Cognit Sci, Daegu, South Korea
[4] Korea Brain Res Inst KBRI, Res Grp Neural Circuit, Daegu, South Korea
基金
新加坡国家研究基金会;
关键词
MICROGLIA; POOL; ELIMINATION; PLASTICITY;
D O I
10.1038/s41586-020-03060-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In adult mice, astrocytes carry out phagocytosis of excitatory hippocampal synapses through MEGF10 to maintain synaptic and circuit homeostasis. In the adult hippocampus, synapses are constantly formed and eliminated(1,2). However, the exact function of synapse elimination in the adult brain, and how it is regulated, are largely unknown. Here we show that astrocytic phagocytosis(3) is important for maintaining proper hippocampal synaptic connectivity and plasticity. By using fluorescent phagocytosis reporters, we find that excitatory and inhibitory synapses are eliminated by glial phagocytosis in the CA1 region of the adult mouse hippocampus. Unexpectedly, we found that astrocytes have a major role in the neuronal activity-dependent elimination of excitatory synapses. Furthermore, mice in which astrocytes lack the phagocytic receptor MEGF10 show a reduction in the elimination of excitatory synapses; as a result, excessive but functionally impaired synapses accumulate. Finally, Megf10-knockout mice show defective long-term synaptic plasticity and impaired formation of hippocampal memories. Together, our data provide strong evidence that astrocytes eliminate unnecessary excitatory synaptic connections in the adult hippocampus through MEGF10, and that this astrocytic function is crucial for maintaining circuit connectivity and thereby supporting cognitive function.
引用
收藏
页码:612 / 617
页数:29
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