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Inhibiting the Mitochondrial Fission Machinery Does Not Prevent Bax/Bak-Dependent Apoptosis

机译:抑制线粒体裂变机制不能阻止Bax / Bak依赖性细胞凋亡。

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摘要

Apoptosis, induced by a number of death stimuli, is associated with a fragmentation of the mitochondrial network. These morphological changes in mitochondria have been shown to require proteins, such as Drp1 or hFis1, which are involved in regulating the fission of mitochondria. However, the precise role of mitochondrial fission during apoptosis remains elusive. Here we report that inhibiting the fission machinery in Bax/Bak-mediated apoptosis, by down-regulating of Drp1 or hFis1, prevents the fragmentation of the mitochondrial network and partially inhibits the release of cytochrome c from the mitochondria but fails to block the efflux of Smac/DIABLO. In addition, preventing mitochondrial fragmentation does not inhibit cell death induced by Bax/Bak-dependent death stimuli, in contrast to the effects of Bcl-xL or caspase inhibition. Therefore, the fission of mitochondria is a dispensable event in Bax/Bak-dependent apoptosis.
机译:由许多死亡刺激物诱导的细胞凋亡与线粒体网络的破碎有关。线粒体的这些形态变化已显示需要蛋白质,例如Drp1或hFis1,它们参与调节线粒体的裂变。但是,线粒体裂变在细胞凋亡过程中的确切作用仍然难以捉摸。在这里,我们报道抑制Bax / Bak介导的凋亡的裂变机制,通过下调Drp1或hFis1,防止线粒体网络断裂,部分抑制线粒体细胞色素c的释放,但不能阻止线粒体的流出。 Smac / DIABLO。此外,与Bcl-xL或caspase抑制作用相反,防止线粒体片段化不会抑制Bax / Bak依赖性死亡刺激诱导的细胞死亡。因此,线粒体的分裂是Bax / Bak依赖性细胞凋亡中不可或缺的事件。

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