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PMID: 19303419 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

A CaPful of mechanisms regulating the mitochondrial permeability transition.

Journal of molecular and cellular cardiology ·Vol. 46 ·No. 6 ·2009-06-00 ·Pages 775-80

Di Lisa F, Bernardi P

Abstract

Despite the lack of its molecular identification, the mitochondrial permeability transition pore (PTP) is a fascinating subject because of its important role in cell death. This holds especially true for cardiovascular diseases and in particular for ischemia-reperfusion injury, where research on PTP inhibition has been successfully translated from bench to clinical evidence of cardioprotection. In addition, recent reports extend the relevance of PTP to heart failure and atherosclerosis. This review summarizes the major factors involved in PTP control with specific emphasis on cardiovascular pathophysiology, and highlights recent findings on the pivotal role of inorganic phosphate as a mediator of the inhibitory effects of cyclosporin A and cyclophilin D ablation.

MeSH Terms
Animals Calcium/metabolism Cyclophilin D Cyclophilins/metabolism Cyclosporine/metabolism Humans Hydrogen-Ion Concentration Mitochondria/metabolism Mitochondrial Membrane Transport Proteins/metabolism Mitochondrial Permeability Transition Pore Models, Biological Phosphates/metabolism,physiology
Chemicals
Cyclophilin D Mitochondrial Membrane Transport Proteins Mitochondrial Permeability Transition Pore Phosphates Cyclosporine Cyclophilins Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Di Lisa Fabio
Department of Biomedical Sciences and CNR Institute of Neuroscience, University of Padova, Padova, Italy. dilisa@bio.unipd.it
Bernardi Paolo
Article Info
Journal
Journal of molecular and cellular cardiology
Abbr.
J Mol Cell Cardiol
ISSN
1095-8584
Published
2009-06-00
Epub
2009-00-19
Pages
775-80
Language
English
Region
England
NLM ID
0262322
Subset
IM
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