Springs Stacy L, Diavolitsis Virginia M, Goodhouse Joseph, McLendon George L
Department of Chemistry and the Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
J Biol Chem. 2002 Nov 29;277(48):45715-8. doi: 10.1074/jbc.C200524200. Epub 2002 Oct 2.
Smac (second mitochondrial activator of caspases) is released from the mitochondria during apoptosis to relieve inhibition of caspases by the inhibitor of apoptosis proteins (IAPs). The release of Smac antagonizes several IAPs and assists the initiator caspase-9 and effector caspases (caspase-3, caspase-6, and caspase-7) in becoming active, ultimately leading to death of the cell. Translocation of Smac along with cytochrome c and other mitochondrial pro-apoptotic proteins represent important regulatory checkpoints for mitochondria-mediated apoptosis. Whether Smac and cytochrome c translocate by the same mechanism is not known. Here, we show that the time required for Smac efflux from the mitochondria of cells subjected to staurosporine-induced apoptosis is approximately four times longer than the time required for cytochrome c efflux. These results suggest that Smac and cytochrome c may exit the mitochondria by different pathways.
Smac(半胱天冬酶的第二种线粒体激活剂)在细胞凋亡期间从线粒体释放,以解除凋亡抑制蛋白(IAPs)对半胱天冬酶的抑制作用。Smac的释放拮抗多种IAPs,并协助起始半胱天冬酶-9和效应半胱天冬酶(半胱天冬酶-3、半胱天冬酶-6和半胱天冬酶-7)激活,最终导致细胞死亡。Smac与细胞色素c及其他线粒体促凋亡蛋白的转位是线粒体介导的细胞凋亡的重要调控检查点。Smac和细胞色素c是否通过相同机制转位尚不清楚。在此,我们表明,在星形孢菌素诱导的细胞凋亡中,Smac从线粒体流出所需的时间大约是细胞色素c流出所需时间的四倍。这些结果表明,Smac和细胞色素c可能通过不同途径离开线粒体。