Reperfusion Injury Salvage Kinase and Survivor Activating Factor Enhancement Prosurvival Signaling Pathways in Ischemic Postconditioning: Two Sides of the Same Coin

被引:172
作者
Hausenloy, Derek J. [1 ]
Lecour, Sandrine [2 ]
Yellon, Derek M. [1 ]
机构
[1] UCL, Hatter Cardiovasc Inst, London WC1E 6HX, England
[2] Univ Cape Town, Dept Med, Fac Hlth Sci, Hatter Cardiovasc Res Inst, ZA-7925 Cape Town, South Africa
关键词
TUMOR-NECROSIS-FACTOR; MITOCHONDRIAL PERMEABILITY TRANSITION; MYOCARDIAL ISCHEMIA/REPERFUSION INJURY; HYPERTHERMIA-INDUCED CARDIOPROTECTION; GLYCOGEN-SYNTHASE KINASE-3-BETA; JAK-STAT PATHWAY; FACTOR-ALPHA; TNF-ALPHA; CELL-DEATH; JAK/STAT PATHWAY;
D O I
10.1089/ars.2010.3360
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The discovery of ischemic postconditioning (IPost) has rejuvenated the field of cardioprotection. As an interventional strategy to be applied at the onset of myocardial reperfusion, the transition of IPost from a bench-side curiosity to potential clinical therapy has been impressively rapid. Its existence also confirms the existence of lethal myocardial reperfusion injury in man, suggesting that 40%-50% of the final reperfused myocardial infarct may actually be due to myocardial reperfusion injury. Intensive analysis of the signal transduction pathways underlying IPost has identified similarities with the signaling pathways underlying its preischemic counterpart, ischemic preconditioning. In this article, the reperfusion injury salvage kinase pathway and the more recently described survivor activating factor enhancement pathway, two apparently distinct signaling pathways that actually interact to convey the IPost stimulus from the cell surface to the mitochondria, where many of the prosurvival and death signals appear to converge. The elucidation of the reperfusion signaling pathways underlying IPost may result in the identification of novel pharmacological targets for cardioprotection. Antioxid. Redox Signal. 14, 893-907.
引用
收藏
页码:893 / +
页数:16
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