| Literature DB >> 26269524 |
Paolo Bernardi1, Andrea Rasola1, Michael Forte1, Giovanna Lippe1.
Abstract
The mitochondrial permeability transition (PT) is a permeability increase of the inner mitochondrial membrane mediated by a channel, the permeability transition pore (PTP). After a brief historical introduction, we cover the key regulatory features of the PTP and provide a critical assessment of putative protein components that have been tested by genetic analysis. The discovery that under conditions of oxidative stress the F-ATP synthases of mammals, yeast, and Drosophila can be turned into Ca(2+)-dependent channels, whose electrophysiological properties match those of the corresponding PTPs, opens new perspectives to the field. We discuss structural and functional features of F-ATP synthases that may provide clues to its transition from an energy-conserving into an energy-dissipating device as well as recent advances on signal transduction to the PTP and on its role in cellular pathophysiology.Entities:
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Year: 2015 PMID: 26269524 PMCID: PMC4600949 DOI: 10.1152/physrev.00001.2015
Source DB: PubMed Journal: Physiol Rev ISSN: 0031-9333 Impact factor: 37.312