Yamaguchi Ryuji, Perkins Guy
Burnham Institute for Medical Science, 10901 N. Torrey Pines Rd., La Jolla, CA 92037, USA.
Biochim Biophys Acta. 2009 Aug;1787(8):963-72. doi: 10.1016/j.bbabio.2009.02.005. Epub 2009 Feb 24.
"The large scale remodeling of mitochondria during apoptosis is a necessary step for the complete release of cytochrome c" has been a tenet since 2002. However, more recent findings strongly indicate that the large-scale remodeling previously described actually takes place after the release of cytochrome c and in a caspase-dependent manner, bringing into question whether mitochondria remodeling is necessary. In a more recent article, however, it was shown that a much more subtle form of remodeling is taking place which is only observable by electron tomography. In the Bcl-2 inhibitable Bax/Bak-dependent intrinsic pathway of apoptosis, the release of cytochrome c from mitochondria is a consequence of two carefully coordinated events: formation of outer membrane pores and opening of crista junctions triggered by Opa1 oligomer disassembly, and both steps are necessary for the complete release of cytochrome c. We review the recent literature pertaining to the coordinated release of cytochrome c during cell death.
自2002年以来,“细胞凋亡过程中线粒体的大规模重塑是细胞色素c完全释放的必要步骤”一直是一个信条。然而,最近的研究结果强烈表明,先前描述的大规模重塑实际上发生在细胞色素c释放之后,并且是以半胱天冬酶依赖的方式进行的,这使得线粒体重塑是否必要受到质疑。然而,在最近的一篇文章中,研究表明正在发生一种更为微妙的重塑形式,这种形式只有通过电子断层扫描才能观察到。在Bcl-2可抑制的Bax/Bak依赖性细胞凋亡内在途径中,细胞色素c从线粒体的释放是两个精心协调的事件的结果:外膜孔的形成和由Opa1寡聚体解体触发的嵴连接的开放,这两个步骤对于细胞色素c的完全释放都是必要的。我们综述了近期有关细胞死亡过程中细胞色素c协同释放的文献。