Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Mitochondrion. 2011 May;11(3):369-81. doi: 10.1016/j.mito.2011.01.010. Epub 2011 Feb 4.
Cytochrome c (Cytc) is essential in mitochondrial electron transport and intrinsic type II apoptosis. Mammalian Cytc also scavenges reactive oxygen species (ROS) under healthy conditions, produces ROS with the co-factor p66(Shc), and oxidizes cardiolipin during apoptosis. The recent finding that Cytc is phosphorylated in vivo underpins a model for the pivotal role of Cytc regulation in making life and death decisions. An apoptotic sequence of events is proposed involving changes in Cytc phosphorylation, increased ROS via increased mitochondrial membrane potentials or the p66(Shc) pathway, and oxidation of cardiolipin by Cytc followed by its release from the mitochondria. Cytc regulation in respiration and cell death is discussed in a human disease context including neurodegenerative and cardiovascular diseases, cancer, and sepsis.
细胞色素 c(Cytc)是线粒体电子传递和固有型细胞凋亡所必需的。在健康条件下,哺乳动物 Cytc 还能清除活性氧(ROS),与辅助因子 p66(Shc)一起产生 ROS,并在凋亡过程中氧化心磷脂。最近发现 Cytc 在体内发生磷酸化,这为 Cytc 调节在生死决策中起关键作用的模型提供了依据。提出了一个凋亡事件的序列,涉及 Cytc 磷酸化的变化、通过增加线粒体膜电位或 p66(Shc)途径增加的 ROS,以及 Cytc 对心磷脂的氧化,随后 Cytc 从线粒体中释放。在涉及神经退行性和心血管疾病、癌症和败血症等人类疾病的背景下,讨论了 Cytc 在呼吸和细胞死亡中的调节。