Iverson Suzanne L, Orrenius Sten
Institute of Environmental Medicine, Division of Toxicology, Karolinska Institutet, Stockholm, Sweden.
Arch Biochem Biophys. 2004 Mar 1;423(1):37-46. doi: 10.1016/j.abb.2003.12.002.
While many studies have focused on cytochrome c release from mitochondria, little attention has been given to the specific interaction between cardiolipin (CL) and cytochrome c, the breaching of which likely represents a critical event in the initiation of mitochondrially mediated apoptosis. Mounting evidence suggests that a decrease in the level of CL affects cytochrome c binding to the inner membrane, thus leading to higher levels of soluble cytochrome c in the mitochondrial intermembrane space. Among the factors known to affect CL levels are thyroid status, plasma concentrations of free fatty acids, Ca2+ dysregulation, and reactive oxygen species (ROS). These factors, especially Ca2+ and ROS, have long been recognized as triggers of cell death and, more recently, as modulators of mitochondrially mediated apoptosis. In this review, we discuss the significance of the disruption of the CL-cytochrome c interaction for cytochrome c release and apoptosis.
虽然许多研究都集中在线粒体中细胞色素c的释放,但对于心磷脂(CL)与细胞色素c之间的特定相互作用却很少关注,这种相互作用的破坏可能是线粒体介导的细胞凋亡起始过程中的一个关键事件。越来越多的证据表明,CL水平的降低会影响细胞色素c与内膜的结合,从而导致线粒体膜间隙中可溶性细胞色素c水平升高。已知影响CL水平的因素包括甲状腺状态、游离脂肪酸的血浆浓度、Ca2+失调和活性氧(ROS)。这些因素,尤其是Ca2+和ROS,长期以来一直被认为是细胞死亡的触发因素,最近又被认为是线粒体介导的细胞凋亡的调节因子。在这篇综述中,我们讨论了CL-细胞色素c相互作用的破坏对细胞色素c释放和细胞凋亡的重要性。