THE MITOCHONDRIAL PERMEABILITY TRANSITION PORE: CHANNEL FORMATION BY F-ATP SYNTHASE, INTEGRATION IN SIGNAL TRANSDUCTION, AND ROLE IN PATHOPHYSIOLOGY

被引:554
作者
Bernardi, Paolo [1 ]
Rasola, Andrea
Forte, Michael
Lippe, Giovanna
机构
[1] Univ Padua, Dept Biomed Sci, Padua, Italy
基金
美国国家卫生研究院;
关键词
PERIPHERAL BENZODIAZEPINE-RECEPTOR; CYTOCHROME-C RELEASE; ADENINE-NUCLEOTIDE TRANSLOCASE; AMYOTROPHIC-LATERAL-SCLEROSIS; BOVINE HEART-MITOCHONDRIA; INHIBITOR PROTEIN IF1; CA-2&-INDUCED MEMBRANE TRANSITION; ISCHEMIA-REPERFUSION INJURY; THERMOPHILIC BACILLUS PS3; DEPENDENT ANION CHANNELS;
D O I
10.1152/physrev.00001.2015
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
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 Ca2+-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.
引用
收藏
页码:1111 / 1155
页数:45
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