Tan Frederick J, Husain Michelle, Manlandro Cara Marie, Koppenol Marijke, Fire Andrew Z, Hill R Blake
Department of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
J Cell Sci. 2008 Oct 15;121(Pt 20):3373-82. doi: 10.1242/jcs.032904. Epub 2008 Sep 30.
Mitochondrial homeostasis reflects a dynamic balance between membrane fission and fusion events thought essential for mitochondrial function. We report here that altered expression of the C. elegans BCL2 homolog CED-9 affects both mitochondrial fission and fusion. Although striated muscle cells lacking CED-9 have no alteration in mitochondrial size or ultrastructure, these cells appear more sensitive to mitochondrial fragmentation. By contrast, increased CED-9 expression in these cells produces highly interconnected mitochondria. This mitochondrial phenotype is partially suppressed by increased expression of the dynamin-related GTPase DRP-1, with suppression dependent on the BH3 binding pocket of CED-9. This suppression suggests that CED-9 directly regulates DRP-1, a model supported by our finding that CED-9 activates the GTPase activity of human DRP1. Thus, CED-9 is capable of regulating the mitochondrial fission-fusion cycle but is not essential for either fission or fusion.
线粒体稳态反映了膜分裂和融合事件之间的动态平衡,而这些事件被认为对线粒体功能至关重要。我们在此报告,秀丽隐杆线虫BCL2同源物CED-9的表达改变会影响线粒体的分裂和融合。尽管缺乏CED-9的横纹肌细胞的线粒体大小或超微结构没有改变,但这些细胞似乎对线粒体碎片化更敏感。相比之下,这些细胞中CED-9表达的增加会产生高度相互连接的线粒体。动力蛋白相关GTP酶DRP-1表达的增加部分抑制了这种线粒体表型,且这种抑制依赖于CED-9的BH3结合口袋。这种抑制表明CED-9直接调节DRP-1,我们发现CED-9激活人DRP1的GTP酶活性这一结果支持了该模型。因此,CED-9能够调节线粒体的分裂-融合循环,但对分裂或融合都不是必需的。