Microglia regulate synaptic development and plasticity

被引:107
作者
Andoh, Megumi [1 ]
Koyama, Ryuta [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Chem Pharmacol Lab, Tokyo, Japan
关键词
microglia; synapse competition; synapse elimination; synapse engulfment; synapse formation; NEURONAL NMDA RECEPTORS; EXTRACELLULAR-MATRIX; BRAIN-INJURY; IN-VIVO; SYNAPSES; ACTIVATION; TREM2; ATP; ELIMINATION; EXPRESSION;
D O I
10.1002/dneu.22814
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Synapses are fundamental structures of neural circuits that transmit information between neurons. Thus, the process of neural circuit formation via proper synaptic connections shapes the basis of brain functions and animal behavior. Synapses continuously undergo repeated formation and elimination throughout the lifetime of an organism, reflecting the dynamics of neural circuit function. The structural transformation of synapses has been described mainly in relation to neural activity-dependent strengthening and weakening of synaptic functions, that is, functional plasticity of synapses. An increasing number of studies have unveiled the roles of microglia, brain-resident immune cells that survey the brain parenchyma with highly motile processes, in synapse formation and elimination as well as in regulating synaptic function. Over the past 15 years, the molecular mechanisms underlying microglia-dependent regulation of synaptic plasticity have been thoroughly studied, and researchers have reported that the disruption of microglia-dependent regulation causes synaptic dysfunction that leads to brain diseases. In this review, we will broadly introduce studies that report the roles of microglia in synaptic plasticity and the possible underlying molecular mechanisms.
引用
收藏
页码:568 / 590
页数:23
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