A dynamic balance of organelle fusion and fission regulates mitochondrial morphology. During apoptosis this balance is altered, leading to an extensive fragmentation of the mitochondria. Here, we describe a novel assay of mitochondrial dynamics based on confocal imaging of cells expressing a mitochondrial matrix–targeted photoactivable green fluorescent protein that enables detection and quantification of organelle fusion in living cells. Using this assay, we visualize and quantitate mitochondrial fusion rates in healthy and apoptotic cells. During apoptosis, mitochondrial fusion is blocked independently of caspase activation. The block in mitochondrial fusion occurs within the same time range as Bax coalescence on the mitochondria and outer mitochondrial membrane permeabilization, and it may be a consequence of Bax/Bak activation during apoptosis.
Quantitation of mitochondrial dynamics by photolabeling of individual organelles shows that mitochondrial fusion is blocked during the Bax activation phase of apoptosis
The online version of this article includes supplemental material.
Abbreviations used in this paper: 3D, three-dimensional; ActD, actinomycin D; mito-PAGFP, mitochondria-targeted PAGFP; MOMP, mitochondrial outer membrane permeabilization; PAGFP, photoactivable GFP; ROI, region of interest; STS, staurosporine; WT MEFs, wild-type mouse embryonic fibroblasts.
Mariusz Karbowski, Damien Arnoult, Hsiuchen Chen, David C. Chan, Carolyn L. Smith, Richard J. Youle; Quantitation of mitochondrial dynamics by photolabeling of individual organelles shows that mitochondrial fusion is blocked during the Bax activation phase of apoptosis . J Cell Biol 16 February 2004; 164 (4): 493–499. doi: https://doi.org/10.1083/jcb.200309082
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