小胶质细胞
生物
神经科学
中枢神经系统
神经炎症
程序性细胞死亡
先天免疫系统
免疫系统
表型
电池类型
免疫学
细胞
细胞凋亡
细胞生物学
炎症
基因
生物化学
遗传学
作者
José L. Marín‐Teva,Miguel A. Cuadros,David Martín‐Oliva,Julio Navascués
出处
期刊:Neuron Glia Biology
[Cambridge University Press]
日期:2011-02-01
卷期号:7 (1): 25-40
被引量:113
标识
DOI:10.1017/s1740925x12000014
摘要
Microglia, the brain's innate immune cell type, are cells of mesodermal origin that populate the central nervous system (CNS) during development. Undifferentiated microglia, also called ameboid microglia, have the ability to proliferate, phagocytose apoptotic cells and migrate long distances toward their final destinations throughout all CNS regions, where they acquire a mature ramified morphological phenotype. Recent studies indicate that ameboid microglial cells not only have a scavenger role during development but can also promote the death of some neuronal populations. In the mature CNS, adult microglia have highly motile processes to scan their territorial domains, and they display a panoply of effects on neurons that range from sustaining their survival and differentiation contributing to their elimination. Hence, the fine tuning of these effects results in protection of the nervous tissue, whereas perturbations in the microglial response, such as the exacerbation of microglial activation or lack of microglial response, generate adverse situations for the organization and function of the CNS. This review discusses some aspects of the relationship between microglial cells and neuronal death/survival both during normal development and during the response to injury in adulthood.
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