| Literature DB >> 29472620 |
Yubin Huang1, Zhen Xu1, Shanshan Xiong1, Fangfang Sun1, Guangrong Qin2, Guanglei Hu1, Jingjing Wang1,3, Lei Zhao1, Yu-Xiang Liang4, Tianzhun Wu1, Zhonghua Lu1, Mark S Humayun5, Kwok-Fai So4,6, Yihang Pan7, Ningning Li7, Ti-Fei Yuan8,9, Yanxia Rao10,11, Bo Peng12.
Abstract
Newborn microglia rapidly replenish the whole brain after selective elimination of most microglia (>99%) in adult mice. Previous studies reported that repopulated microglia were largely derived from microglial progenitor cells expressing nestin in the brain. However, the origin of these repopulated microglia has been hotly debated. In this study, we investigated the origin of repopulated microglia by a series of fate-mapping approaches. We first excluded the blood origin of repopulated microglia via parabiosis. With different transgenic mouse lines, we then demonstrated that all repopulated microglia were derived from the proliferation of the few surviving microglia (<1%). Despite a transient pattern of nestin expression in newly forming microglia, none of repopulated microglia were derived from nestin-positive non-microglial cells. In summary, we conclude that repopulated microglia are solely derived from residual microglia rather than de novo progenitors, suggesting the absence of microglial progenitor cells in the adult brain.Entities:
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Year: 2018 PMID: 29472620 DOI: 10.1038/s41593-018-0090-8
Source DB: PubMed Journal: Nat Neurosci ISSN: 1097-6256 Impact factor: 24.884