线粒体分裂
生物
线粒体凋亡诱导通道
细胞生物学
DNM1L型
线粒体融合
细胞器
线粒体
细胞凋亡
胞浆
动力素
内质网
DNAJA3公司
粒体自噬
MFN2型
程序性细胞死亡
线粒体内膜
MFN1型
调解人
细胞色素c
膜间隙
细胞
线粒体DNA
生物化学
内吞作用
基因
酶
作者
Stephan Frank,Brigitte Gaume,Elke S. Bergmann‐Leitner,Wolfgang W. Leitner,Everett G. Robert,Frédéric Catez,Carolyn L. Smith,Richard J. Youle
标识
DOI:10.1016/s1534-5807(01)00055-7
摘要
In healthy cells, fusion and fission events participate in regulating mitochondrial morphology. Disintegration of the mitochondrial reticulum into multiple punctiform organelles during apoptosis led us to examine the role of Drp1, a dynamin-related protein that mediates outer mitochondrial membrane fission. Upon induction of apoptosis, Drp1 translocates from the cytosol to mitochondria, where it preferentially localizes to potential sites of organelle division. Inhibition of Drp1 by overexpression of a dominant-negative mutant counteracts the conversion to a punctiform mitochondrial phenotype, prevents the loss of the mitochondrial membrane potential and the release of cytochrome c, and reveals a reproducible swelling of the organelles. Remarkably, inhibition of Drp1 blocks cell death, implicating mitochondrial fission as an important step in apoptosis.
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