Microglial and macrophage polarization -new prospects for brain repair

被引:1195
作者
Hu, Xiaoming [1 ]
Leak, Rehana K. [1 ]
Shi, Yejie [1 ]
Suenaga, Jun [1 ]
Gao, Yanqin [2 ,3 ]
Zheng, Ping [2 ,3 ]
Chen, Jun [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Ctr Cerebrovasc Dis Res, Pittsburgh, PA 15213 USA
[2] Fudan Univ, State Key Lab Med Neurobiol, Shanghai 200032, Peoples R China
[3] Fudan Univ, Inst Brain Sci, Shanghai 200032, Peoples R China
关键词
ACTIVATED-RECEPTOR-GAMMA; ALTERNATIVE M2 MACROPHAGES; CEREBRAL-ISCHEMIA; IN-VIVO; CELL PROLIFERATION; PHENOTYPE MARKERS; SIGNAL TRANSDUCER; HEME OXYGENASE-1; WHITE-MATTER; INJURY;
D O I
10.1038/nrneurol.2014.207
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The traditional view of the adult brain as a static organ has changed in the past three decades, with the emergence of evidence that it remains plastic and has some regenerative capacity after injury. In the injured brain, microglia and macrophages clear cellular debris and orchestrate neuronal restorative processes. However, activation of these cells can also hinder CNS repair and expand tissue damage. Polarization of macrophage populations toward different phenotypes at different stages of injury might account for this dual role. This Perspectives article highlights the specific roles of polarized microglial and macrophage populations in CNS repair after acute injury, and argues that therapeutic approaches targeting cerebral inflammation should shift from broad suppression of microglia and macrophages towards subtle adjustment of the balance between their phenotypes. Breakthroughs in the identification of regulatory molecules that control these phenotypic shifts could ultimately accelerate research towards curing brain disorders.
引用
收藏
页码:56 / 64
页数:9
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