Role for CED-9 and Egl-1 as regulators of mitochondrial fission and fusion dynamics

被引:174
作者
Delivani, P [1 ]
Adrain, C [1 ]
Taylor, RC [1 ]
Duriez, PJ [1 ]
Martin, SJ [1 ]
机构
[1] Trinity Coll Dublin, Smurfit Inst, Dept Genet, Mol Cell Biol Lab, Dublin 2, Ireland
基金
爱尔兰科学基金会;
关键词
D O I
10.1016/j.molcel.2006.01.034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BcI-2 family proteins play central roles in apoptosis by regulating the release of mitochondrial intermembrane space proteins such as cytochrome c. Death-promoting BcI-2 family members, such as Bax, can promote cytochrome c release and fragmentation of the mitochondrial network, whereas apoptosis-inhibitory members, such as BcI-2 and Bcl-xL, can antagonize these events. It remains unclear whether CED-9, the worm BcI-2 relative, can regulate mitochondrial fission/fusion dynamics or the release of proteins from the mitochondrial intermembrane space. Here, we show that CED-9 interacts with Mitofusin-2/fuzzy onions and can promote mitochondrial clustering and dramatic reorganization of mitochondrial networks. Consistent with its ability to neutralize CED-9 function, EGL-1 antagonized CED-9-dependent remodeling of the mitochondrial network. However, CED-9 failed to inhibit mitochondrial cytochrome c release or apoptosis induced by diverse triggers in mammalian cells. These data suggest that the ability to regulate mitochondrial fission/fusion dynamics is an evolutionarily conserved property of the BcI-2 family.
引用
收藏
页码:761 / 773
页数:13
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