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小胶质细胞调节突触发育和可塑性。

Microglia regulate synaptic development and plasticity.

机构信息

Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.

出版信息

Dev Neurobiol. 2021 Jul;81(5):568-590. doi: 10.1002/dneu.22814. Epub 2021 Mar 8.

Abstract

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.

摘要

突触是神经元之间传递信息的神经回路的基本结构。因此,通过适当的突触连接形成神经回路的过程构成了大脑功能和动物行为的基础。突触在生物体的整个生命周期中不断经历反复的形成和消除,反映了神经回路功能的动态变化。突触的结构转换主要与神经活动依赖性的突触功能增强和减弱有关,即突触的功能可塑性。越来越多的研究揭示了小胶质细胞在突触形成和消除以及调节突触功能中的作用,小胶质细胞是一种具有高度运动性的脑内常驻免疫细胞。在过去的 15 年中,人们对小胶质细胞依赖性调节突触可塑性的分子机制进行了深入研究,并报道了小胶质细胞依赖性调节的破坏会导致导致脑部疾病的突触功能障碍。在这篇综述中,我们将广泛介绍报道小胶质细胞在突触可塑性中的作用及其潜在的分子机制的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b94c/8451802/18616bef4075/DNEU-81-568-g001.jpg

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