Cell Death Mechanisms in Cerebral Ischemia-Reperfusion Injury

被引:158
作者
Zhang, Qian [1 ,2 ,3 ,4 ]
Jia, Meng [2 ,3 ,4 ]
Wang, YunFu [5 ]
Wang, Qun [2 ,4 ]
Wu, Jianping [1 ,2 ,3 ,4 ]
机构
[1] Wuhan Univ Technol, Sch Chem Chem Engn & Life Sci, Wuhan 430070, Peoples R China
[2] Capital Med Univ, Beijing Tiantan Hosp, Beijing 100070, Peoples R China
[3] Capital Med Univ, Adv Innovat Ctr Human Brain Protect, Beijing 100070, Peoples R China
[4] Natl Clin Res Ctr Neurol Dis, Beijing 100070, Peoples R China
[5] Hubei Univ Med, Taihe Hosp, Shiyan 440070, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Cerebral ischemia-reperfusion; Apoptosis; Necrosis; Necroptosis; Autophagy; MITOCHONDRIAL PERMEABILITY TRANSITION; TISSUE-PLASMINOGEN ACTIVATOR; BCL-2 FAMILY PROTEINS; PROGRAMMED NECROSIS; ISCHEMIA/REPERFUSION INJURY; UP-REGULATION; INFLAMMASOME ACTIVATION; NUCLEAR TRANSLOCATION; HIPPOCAMPAL-NEURONS; THERAPEUTIC TARGET;
D O I
10.1007/s11064-022-03697-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ischemic stroke is one of the major causes of morbidity and mortality, affecting millions of people worldwide. Inevitably, the interruption of cerebral blood supply after ischemia may promote a cascade of pathophysiological processes. Moreover, the subsequent restoration of blood flow and reoxygenation may further aggravate brain tissue injury. Although recombinant tissue plasminogen activator (rt-PA) is the only approved therapy for restoring blood perfusion, the reperfusion injury and the narrow therapeutic time window restrict its application for most stroke patients. Increasing evidence indicates that multiple cell death mechanisms are relevant to cerebral ischemia-reperfusion injury, including apoptosis, necrosis, necroptosis, autophagy, pyroptosis, ferroptosis, and so on. Therefore, it is crucial to comprehend various cell death mechanisms and their interactions. In this review, we summarize the various signaling pathways underlying cerebral ischemia-reperfusion injury and elaborate on the crosstalk between the different mechanisms.
引用
收藏
页码:3525 / 3542
页数:18
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