小胶质细胞
单核吞噬细胞系统
生物
祖细胞
巨噬细胞
命运图
胚胎干细胞
造血
细胞生物学
人口
中枢神经系统
免疫学
神经科学
干细胞
炎症
医学
基因
遗传学
体外
环境卫生
作者
Florent Ginhoux,Melanie Greter,Marylène Leboeuf,Sayan Nandi,Peter See,Şölen Gökhan,Mark F. Mehler,Simon J. Conway,Lai Guan Ng,E. Richard Stanley,Igor M. Samokhvalov,Miriam Mérad
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2010-10-22
卷期号:330 (6005): 841-845
被引量:4478
标识
DOI:10.1126/science.1194637
摘要
Microglia are the resident macrophages of the central nervous system and are associated with the pathogenesis of many neurodegenerative and brain inflammatory diseases; however, the origin of adult microglia remains controversial. We show that postnatal hematopoietic progenitors do not significantly contribute to microglia homeostasis in the adult brain. In contrast to many macrophage populations, we show that microglia develop in mice that lack colony stimulating factor-1 (CSF-1) but are absent in CSF-1 receptor-deficient mice. In vivo lineage tracing studies established that adult microglia derive from primitive myeloid progenitors that arise before embryonic day 8. These results identify microglia as an ontogenically distinct population in the mononuclear phagocyte system and have implications for the use of embryonically derived microglial progenitors for the treatment of various brain disorders.
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