Kessel D, Luo Y
Department of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.
Cell Death Differ. 1999 Jan;6(1):28-35. doi: 10.1038/sj.cdd.4400446.
Photodamage to the mitochondria of murine leukemia P388 cells resulted in immediate loss of the mitochondrial membrane potential together with the release of cytochrome c into the cytosol. This was followed by a rapid activation of caspase 3-like proteases, as indicated by a marked rise in DEVDase activity. There was no significant effect on WEHDase or VEIDase activities, suggesting that only the late-stage caspases had been effected. The apoptotic response to mitochondrial photodamage was abolished by the broad-spectrum caspase inhibitor zVAD-fmk, but this did not prevent loss of viability after mitochondrial photodamage. These studies indicate that the release of cytochrome c from photodamaged mitochondria is sufficient to directly initiate a caspase-dependent apoptotic response.
鼠白血病P388细胞线粒体的光损伤导致线粒体膜电位立即丧失,同时细胞色素c释放到细胞质中。随后,如DEVDase活性显著升高所示,caspase 3样蛋白酶迅速激活。对WEHDase或VEIDase活性没有显著影响,表明仅晚期半胱天冬酶受到影响。广谱半胱天冬酶抑制剂zVAD-fmk消除了对线粒体光损伤的凋亡反应,但这并不能防止线粒体光损伤后细胞活力的丧失。这些研究表明,光损伤线粒体释放的细胞色素c足以直接引发半胱天冬酶依赖性凋亡反应。