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缺血预处理和后处理中的连接蛋白43

Connexin 43 in ischemic pre- and postconditioning.

作者信息

Schulz Rainer, Boengler Kerstin, Totzeck Andreas, Luo Yukun, Garcia-Dorado David, Heusch Gerd

机构信息

Institut für Pathophysiologie, Zentrum für Innere Medizin, Universitätsklinikum Essen, Hufelandstrasse 55, 45122 Essen, Germany.

出版信息

Heart Fail Rev. 2007 Dec;12(3-4):261-6. doi: 10.1007/s10741-007-9032-3.

Abstract

Connexin 43 (Cx43) is the predominant protein forming gap junctions and non-junctional hemichannels in ventricular myocardium, but Cx43 is also localized at the inner membrane of cardiomyocyte mitochondria. In cardiomyocytes, Cx43 is involved in the formation of reactive oxygen species, which are central to the signal transduction cascade of ischemic preconditioning's protection. Accordingly, genetically-induced or age-related loss of Cx43 abolishes infarct size reduction by ischemic preconditioning. Similarly, mitochondrial import inhibition of Cx43 completely blocks infarct size reduction by pharmacological preconditioning with diazoxide. In contrast to its importance for preconditioning-induced cardioprotection, Cx43 is not important for infarct size reduction by ischemic postconditioning. In summary, Cx43--especially Cx43 localized in mitochondria--appears to be one key element of the signal transduction cascade of the protection by preconditioning.

摘要

连接蛋白43(Cx43)是在心室心肌中形成缝隙连接和非连接半通道的主要蛋白质,但Cx43也定位于心肌细胞线粒体的内膜。在心肌细胞中,Cx43参与活性氧的形成,而活性氧是缺血预处理保护信号转导级联反应的核心。因此,基因诱导或与年龄相关的Cx43缺失会消除缺血预处理对梗死面积的缩小作用。同样,对Cx43的线粒体导入抑制会完全阻断用二氮嗪进行药理预处理对梗死面积的缩小作用。与其对预处理诱导的心脏保护的重要性相反,Cx43对缺血后处理减少梗死面积并不重要。总之,Cx43——尤其是定位于线粒体的Cx43——似乎是预处理保护信号转导级联反应的一个关键要素。

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