脉络丛
中枢神经系统
生物
小胶质细胞
细胞生物学
薄壁组织
转录因子
造血
免疫系统
巨噬细胞
命运图
血脑屏障
病理
免疫学
神经科学
炎症
医学
干细胞
遗传学
基因
祖细胞
体外
植物
作者
Tobias Goldmann,Peter Wieghofer,Marta Joana Costa Jordão,Fabiola Prutek,Nora Hagemeyer,Kathrin Frenzel,Lukas Amann,Ori Staszewski,Katrin Kierdorf,Martin Krueger,Giuseppe Locatelli,Hannah Hochgerner,Robert Zeiser,Slava Epelman,Frédéric Geissmann,Josef Priller,Fábio Rossi,Ingo Bechmann,Martin Kerschensteiner,Sten Linnarsson,Steffen Jung,Marco Prinz
摘要
Microglia progenitors seed the central nervous system from the yolk sac, but little is known about the origin of non-parenchymal macrophages. Prinz and colleagues demonstrate that these macrophages in the central nervous system are related to but distinct from microglia and are largely of embryonic origin. Perivascular, subdural meningeal and choroid plexus macrophages are non-parenchymal macrophages that mediate immune responses at brain boundaries. Although the origin of parenchymal microglia has recently been elucidated, much less is known about the precursors, the underlying transcriptional program and the dynamics of the other macrophages in the central nervous system (CNS). It was assumed that they have a high turnover from blood-borne monocytes. However, using parabiosis and fate-mapping approaches in mice, we found that CNS macrophages arose from hematopoietic precursors during embryonic development and established stable populations, with the notable exception of choroid plexus macrophages, which had dual origins and a shorter life span. The generation of CNS macrophages relied on the transcription factor PU.1, whereas the MYB, BATF3 and NR4A1 transcription factors were not required.
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