Brooks Craig, Dong Zheng
Department of Cellular Biology and Anatomy, Medical College of Georgia and Veterans Affairs Medical Center, Augusta, Georgia 30912, USA.
Cell Cycle. 2007 Dec 15;6(24):3043-7. doi: 10.4161/cc.6.24.5115. Epub 2007 Oct 2.
Early during apoptosis, the mitochondrial network collapses into short punctuate fragments. The seemingly morphological change, called mitochondrial fragmentation, contributes to mitochondrial injury. Mitochondrial morphology is dictated by two opposing processes, fission and fusion. It is unclear how the fission-fusion balance is tilted during apoptosis, resulting in mitochondrial fragmentation. Emerging evidence has now suggested a regulation of mitochondrial morphological dynamics by Bcl-2 family proteins. In this regulation, Bak appears to be a key. Through interaction with mitofusins, Bak may block mitochondrial fusion to induce fragmentation. By this function, Bak may collaborate with Bax to permeabilize mitochondrial outer membrane, leading to the release of apoptogenic factors.
在细胞凋亡早期,线粒体网络会瓦解成短的点状片段。这种看似形态上的变化,即所谓的线粒体碎片化,会导致线粒体损伤。线粒体形态由两种相反的过程决定,即裂变和融合。目前尚不清楚在细胞凋亡过程中裂变 - 融合平衡是如何倾斜从而导致线粒体碎片化的。新出现的证据表明,Bcl - 2家族蛋白对线粒体形态动力学具有调控作用。在这种调控中,Bak似乎是关键因素。通过与线粒体融合蛋白相互作用,Bak可能会阻断线粒体融合以诱导碎片化。通过这一功能,Bak可能与Bax协同作用使线粒体外膜通透化,从而导致凋亡因子的释放。