Microglia regulate synaptic development and plasticity

神经科学 突触可塑性 生物 小胶质细胞 突触 变质塑性 生物神经网络 突触标度 神经可塑性 受体 免疫学 炎症 生物化学
作者
Megumi Andoh,Ryuta Koyama
出处
期刊:Developmental Neurobiology [Wiley]
卷期号:81 (5): 568-590 被引量:115
标识
DOI:10.1002/dneu.22814
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.

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