小胶质细胞
炎症
生物
中枢神经系统
背景(考古学)
吞噬作用
神经科学
巨噬细胞
免疫学
脊髓损伤
单核细胞
细胞生物学
脊髓
体外
生物化学
古生物学
作者
Andrew D. Greenhalgh,Juan G. Zarruk,Luke M. Healy,Sam Joshva Baskar Jesudasan,Priya Jhelum,Christopher Salmon,Albert Formanek,Matthew V. Russo,Jack P. Antel,Dorian B. McGavern,Barry W. McColl,Samuel David
出处
期刊:PLOS Biology
[Public Library of Science]
日期:2018-10-17
卷期号:16 (10): e2005264-e2005264
被引量:164
标识
DOI:10.1371/journal.pbio.2005264
摘要
Infiltrating monocyte-derived macrophages (MDMs) and resident microglia dominate central nervous system (CNS) injury sites. Differential roles for these cell populations after injury are beginning to be uncovered. Here, we show evidence that MDMs and microglia directly communicate with one another and differentially modulate each other’s functions. Importantly, microglia-mediated phagocytosis and inflammation are suppressed by infiltrating macrophages. In the context of spinal cord injury (SCI), preventing such communication increases microglial activation and worsens functional recovery. We suggest that macrophages entering the CNS provide a regulatory mechanism that controls acute and long-term microglia-mediated inflammation, which may drive damage in a variety of CNS conditions.
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