Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9884704 | Biochimica et Biophysica Acta (BBA) - Bioenergetics | 2005 | 13 Pages |
Abstract
The inner mitochondrial membrane is famously impermeable to solutes not provided with a specific carrier. When this impermeability is lost, either in a developmental context or under stress, the consequences for the cell can be far-reaching. Permeabilization of isolated mitochondria, studied since the early days of the field, is often discussed as if it were a biochemically well-defined phenomenon, occurring by a unique mechanism. On the contrary, evidence has been accumulating that it may be the common outcome of several distinct processes, involving different proteins or protein complexes, depending on circumstances. A clear definition of this putative variety is a prerequisite for an understanding of mitochondrial permeabilization within cells, of its roles in the life of organisms, and of the possibilities for pharmacological intervention.
Keywords
VDACmitochondrial megachannelPhAsOCarboxyatractylosideTFPCypDCATRCyclophilin DpA2GSK-3βPTPMCCMMCANTROSphospholipase A2Permeability transition porePermeability transitionCSABaxadenine nucleotide translocatoradenine nucleotide transportercyclosporin AMitochondriahexokinaseProtein importProtein kinaseCreatine kinaseGlycogen synthase kinase 3βReactive oxygen species
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Authors
Mario Zoratti, Ildikò Szabò, Umberto De Marchi,