Inhibition of TIM-4 protects against cerebral ischaemia-reperfusion injury

被引:8
|
作者
Zheng, Lifang [1 ,2 ]
Huang, Yongqian [2 ]
Wang, Xinghua [2 ]
Wang, Xijia [2 ]
Chen, Wei [3 ]
Cheng, Wei [2 ]
Pan, Chunlian [2 ]
机构
[1] Seventh Peoples Hosp Shenzhen, Dept Neurol, Shenzhen, Guangdong, Peoples R China
[2] Wuhan Univ Sci & Technol, Dept Neurol, Puren Hosp, Wuhan, Hubei, Peoples R China
[3] Zhejiang Acad Tradit Chinese Med, Canc Inst Integrated Tradit Chinese & Western Med, Key Lab Canc Prevent & Therapy Combining Tradit C, Hangzhou, Zhejiang, Peoples R China
关键词
cerebral ischaemia-reperfusion injury; co-culture; TIM-4; ARTERY OCCLUSION; STROKE; MODEL; PHOSPHATIDYLSERINE; MECHANISMS; MICE;
D O I
10.1111/jcmm.14754
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
TIM-4 plays an important role in ischaemia-reperfusion injury of liver and kidney; however, the effects of TIM-4 on cerebral ischaemia-reperfusion injury (IRI) are unknown. The purpose of the present study was to investigate the potential role of TIM-4 in experimental brain ischaemia-reperfusion injury. In this study, cerebral ischaemia reperfusion was induced by transient middle cerebral artery occlusion (MCAO) for 1 hour in C57/BL6 mice. The TIM-4 expression was detected in vivo or vitro by real-time quantitative polymerase chain reaction, Western blot and flow cytometric analysis. In vivo, the administration of anti-TIM-4 antibodies significantly suppressed apoptosis, inhibited inflammatory cells and enhanced anti-inflammatory responses. In vitro, activated microglia exhibited reduced cellular proliferation and induced IRI injury when co-cultured with neurons; these effects were inhibited by anti-TIM-4 antibody treatment. Similarly, microglia transfected with TIM-4 siRNA and stimulated by LPS + IFN-gamma alleviated the TIM-4-mediated damage to neurons. Collectively, our data indicate that the inhibition of TIM-4 can improve the inflammatory response and exerts a protective effect in cerebral ischaemia-reperfusion injury.
引用
收藏
页码:1276 / 1285
页数:10
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