Homeostasis of Microglia in the Adult Brain: Review of Novel Microglia Depletion Systems

被引:145
|
作者
Waisman, Ari [1 ]
Ginhoux, Florent [2 ]
Greter, Melanie [3 ]
Bruttger, Julia [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Mol Med, D-55131 Mainz, Germany
[2] ASTAR, Singapore Immunol Network SIgN, Singapore 138648, Singapore
[3] Univ Zurich, Inst Expt Immunol, CH-8057 Zurich, Switzerland
关键词
CENTRAL-NERVOUS-SYSTEM; TISSUE-RESIDENT MACROPHAGES; YOLK-SAC; FRACTALKINE RECEPTOR; TARGETED DISRUPTION; DENDRITIC CELLS; SELF-RENEWAL; MOUSE-BRAIN; STEM-CELLS; IN-VIVO;
D O I
10.1016/j.it.2015.08.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Microglia are brain macrophages that emerge from early erythro-myeloid precursors in the embryonic yolk sac and migrate to the brain mesenchyme before the blood brain barrier is formed. They seed the brain, and proliferate until they have formed a grid-like distribution in the central nervous system that is maintained throughout lifespan. The mechanisms through which these embryonic-derived cells contribute to microglia homoeostasis at steady state and upon inflammation are still not entirely clear. Here we review recent studies that provided insight into the contribution of embryonically-derived microglia and of adult 'microglia-like' cells derived from monocytes during inflammation. We examine different microglia depletion models, and discuss the origin of their rapid repopulation after depletion and outline important areas of future research.
引用
收藏
页码:625 / 636
页数:12
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