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脑缺血/再灌注过程中凋亡启动子和抑制剂(Smac/DIABLO和XIAP)的亚细胞定位。

Subcellular localization of a promoter and an inhibitor of apoptosis (Smac/DIABLO and XIAP) during brain ischemia/reperfusion.

作者信息

Shibata Mamoru, Hattori Hidenori, Sasaki Takahiro, Gotoh Jun, Hamada Junichi, Fukuuchi Yasuo

机构信息

Department of Neurology, Saitama National Hospital, Japan.

出版信息

Neuroreport. 2002 Oct 28;13(15):1985-8. doi: 10.1097/00001756-200210280-00031.

Abstract

We explored the expression of Smac/DIABLO, a newly identified mitochondrial apoptogenic molecule, and X-linked inhibitor of apoptosis protein (XIAP) in the brain subjected to ischemia/reperfusion. Transient focal ischemia was produced for 1 hour in mice. We observed only a negligible amount of Smac/DIABLO in both mitochondria and cytosol in the normal state. The mitochondrial expression level of Smac/DIABLO increased after 2-11 h reperfusion. There was increased Smac/DIABLO expression in the cytosol after 5 h reperfusion, implying the translocation of Smac/DIABLO into the cytosol. The subcellular localization of XIAP became more extensive within the cells during reperfusion, as compared with the normal state. Our results imply that Smac/DIABLO and XIAP are implicated in the pathophysiological mechanisms of reperfusion injury.

摘要

我们探究了新近发现的线粒体凋亡分子Smac/DIABLO以及X连锁凋亡抑制蛋白(XIAP)在脑缺血/再灌注中的表达情况。对小鼠进行1小时的短暂局灶性缺血。我们观察到在正常状态下,线粒体和细胞质中Smac/DIABLO的含量极少。再灌注2 - 11小时后,Smac/DIABLO的线粒体表达水平升高。再灌注5小时后,细胞质中Smac/DIABLO的表达增加,这意味着Smac/DIABLO转位至细胞质中。与正常状态相比,再灌注期间XIAP在细胞内的亚细胞定位范围更广。我们的结果表明,Smac/DIABLO和XIAP参与了再灌注损伤的病理生理机制。

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