Wang Shulin, El-Deiry Wafik S
Laboratory of Molecular Oncology and Cell Cycle Regulation, Howard Hughes Medical Institute, Department of Medicine, Abramson Cancer Center, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Cancer Biol Ther. 2004 Jan;3(1):44-6. doi: 10.4161/cbt.3.1.740. Epub 2004 Jan 31.
Early and pivotal events in apoptosis are now known to occur in the mitochondria and the endoplasmic reticulum, and release of cytochrome c from the mitochondria and calcium from the endoplasmic recticulum into the cytosol are considered to be requisites for apoptosis in response to different stimuli. In the December 2003 issue of Nature Cell Biology, Boehning et al. report that early in apoptosis mitochondrial cyctochrome c translocates to the endoplasmic reticulum where it specifically binds inositol (1,4,5) triphosphate receptors, leading to sustained calcium release. The released calcium then triggers a mass exodus of cytochrome c from all mitochondria in the cells, thus amplifying the apoptotic signal.
现在已知细胞凋亡早期的关键事件发生在线粒体和内质网中,线粒体释放细胞色素c以及内质网释放钙到细胞质中被认为是细胞对不同刺激作出凋亡反应的必要条件。在2003年12月的《自然细胞生物学》杂志上,博宁等人报道,在细胞凋亡早期,线粒体细胞色素c转移到内质网,在那里它特异性结合肌醇(1,4,5)三磷酸受体,导致钙持续释放。释放的钙随后触发细胞中所有线粒体的细胞色素c大量外流,从而放大凋亡信号。