小胶质细胞
特雷姆2
吞噬作用
受体
生物
冲程(发动机)
神经科学
免疫系统
中枢神经系统
炎症
医学
免疫学
细胞生物学
生物化学
机械工程
工程类
作者
Wen-yu Ma,Shasha Wang,Qinglin Wu,Xin‐Fu Zhou,Shifeng Chu,Nai‐Hong Chen
标识
DOI:10.1016/j.intimp.2022.108733
摘要
Microglia are the earliest activated and the longest lasting immune cells after stroke, and they participate in almost all the pathological reactions after stroke. However, their regulatory mechanism has not been fully elucidated. Triggering receptor expressed on myeloid cells-2 (TREM2) is a cell surface receptor that is mainly expressed in microglia of the central nervous system. The receptor plays an important role in regulating microglia energy metabolism and phenotypic transformation. At present, TREM2 has been developed as a potential target for AD, coronary atherosclerosis and other diseases. However, TREM2 does not provide a systematic summary of the functional transformation and intrinsic molecular mechanisms of microglia after stroke. In this paper, we have summarized the functional changes of TREM2 in microglia after stroke in recent years, and found that TREM2 has important effects on energy metabolism, phagocytosis and anti-inflammatory function of microglia after stroke, suggesting that TREM2 is a potential therapeutic target for the treatment of stroke.
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