小胶质细胞
神经科学
平衡
生物
大脑发育
人口
人脑
脑功能
发病机制
中枢神经系统
功能(生物学)
医学
免疫学
细胞生物学
炎症
环境卫生
作者
Diego Gómez‐Nicola,Gemma L. Fryatt,Katharine E. Askew
出处
期刊:Methods in molecular biology
日期:2019-01-01
卷期号:: 207-215
被引量:2
标识
DOI:10.1007/978-1-4939-9658-2_15
摘要
Microglia are the main resident immunocompetent cells of the brain with key roles in brain development, homeostasis, and function. Recent reports have started to shed light on the homeostatic mechanisms regulating the composition and turnover of the microglial population under physiological conditions from development to ageing, but our knowledge of the dynamics of microglia is incomplete. Therefore, it appears relevant to provide a standardized approach to quantify the turnover of microglia, with direct application to create a greater understanding of the dynamics of this cell population, and how it may contribute to the pathogenesis and/or progression of neurological disorders. Here we describe a robust immunohistochemical method to analyze microglial proliferation in mouse brain, aiming at providing a shared and universal approach to analyze microglial dynamics across different laboratories.
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