Matapurkar A, Lazebnik Y
Cold Spring Harbor Laboratory, One Bungtown Rd, Cold Spring Harbor, NY 11724, USA.
Cell Death Differ. 2006 Dec;13(12):2062-7. doi: 10.1038/sj.cdd.4401968. Epub 2006 May 26.
During apoptosis, cytochrome c released from mitochondria activates Apaf-1, a cofactor of caspase-9. The evidence that cytochrome c can activate Apaf-1 is abundant, but the proof that cytochrome c is required for apoptosis is limited to two studies that used genetically modified mice. One of these studies concluded that in some tissues apoptosis may require Apaf-1 but not cytochrome c, which indicated the need to analyze the requirement of cytochrome c beyond the mouse models, and in human tumor cells in particular. In this study, we designed tools to silence cytochrome c expression in human cells and tested these tools in an experimental system of oncogenic transformation. We found that cytochrome c was required for apoptosis induced by both DNA damage and, unexpectedly, TNFalpha. Overall, this study established that cytochrome c is required for apoptosis in human cells and provided tools to dissect mechanisms of apoptosis in various experimental models.
在细胞凋亡过程中,从线粒体释放的细胞色素c激活凋亡蛋白酶激活因子-1(Apaf-1),它是半胱天冬酶-9的一个辅助因子。细胞色素c能够激活Apaf-1的证据很多,但细胞色素c是细胞凋亡所必需的这一证据仅限于两项使用基因改造小鼠的研究。其中一项研究得出结论,在某些组织中,细胞凋亡可能需要Apaf-1,但不需要细胞色素c,这表明需要在小鼠模型之外,特别是在人类肿瘤细胞中分析细胞色素c的需求情况。在本研究中,我们设计了使人类细胞中细胞色素c表达沉默的工具,并在致癌转化实验系统中对这些工具进行了测试。我们发现,DNA损伤以及出乎意料的肿瘤坏死因子α(TNFalpha)诱导的细胞凋亡均需要细胞色素c。总体而言,本研究证实细胞色素c是人类细胞凋亡所必需的,并提供了在各种实验模型中剖析细胞凋亡机制的工具。