The mitochondrial permeability transition pore and its involvement in cell death and in disease pathogenesis

被引:448
作者
Rasola, Andrea
Bernardi, Paolo
机构
[1] Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy
[2] Univ Padua, Dept Biomed Sci, I-35121 Padua, Italy
关键词
apoptosis; mitochondria; permeability transition pore;
D O I
10.1007/s10495-007-0723-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current research on the mitochondrial permeability transition pore (PTP) and its role in cell death faces a paradox. Initially considered as an in vitro artifact of little pathophysiological relevance, in recent years the PTP has received considerable attention as a potential mechanism for the execution of cell death. The recent successful use of PTP desensitizers in several disease paradigms leaves little doubt about its relevance in pathophysiology; and emerging findings that link the PTP to key cellular signalling pathways are increasing the interest on the pore as a pharmacological target. Yet, recent genetic data have challenged popular views on the molecular nature of the PTP, and called into question many early conclusions about its structure. Here we review basic concepts about PTP structure, function and regulation within the framework of intracellular death signalling, and its role in disease pathogenesis.
引用
收藏
页码:815 / 833
页数:19
相关论文
共 260 条
[1]   Cyclosporin A improves brain tissue oxygen consumption and learning/memory performance after lateral fluid percussion injury in rats [J].
Alessandri, B ;
Rice, AC ;
Levasseur, J ;
DeFord, M ;
Hamm, RJ ;
Bullock, MR .
JOURNAL OF NEUROTRAUMA, 2002, 19 (07) :829-841
[2]  
ANGELIN A, 2007, IN PRESS P NATL 0110
[3]   GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[4]   There is more to life and death than mitochondria: Bcl-2 proteins at the endoplasmic reticulum [J].
Annis, MG ;
Yethon, JA ;
Leber, B ;
Andrews, DW .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1644 (2-3) :115-123
[5]   Inhibition of Bax channel-forming activity by Bcl-2 [J].
Antonsson, B ;
Conti, F ;
Ciavatta, A ;
Montessuit, S ;
Lewis, S ;
Martinou, I ;
Bernasconi, L ;
Bernard, A ;
Mermod, JJ ;
Mazzei, G ;
Maundrell, K ;
Gambale, F ;
Sadoul, R ;
Martinou, JC .
SCIENCE, 1997, 277 (5324) :370-372
[6]  
Argaud Laurent, 2005, J Mol Cell Cardiol, V38, P367, DOI 10.1016/j.yjmcc.2004.12.001
[7]   The role of the mitochondrial permeability transition in cell death [J].
Armstrong, Jeffrey S. .
MITOCHONDRION, 2006, 6 (05) :225-234
[8]   In self-defence: Hexokinase promotes voltage-dependent anion channel closure and prevents mitochondria-mediated apoptotic cell death [J].
Azoulay-Zohar, H ;
Israelson, A ;
Abu-Hamad, S ;
Shoshan-Barmatz, V .
BIOCHEMICAL JOURNAL, 2004, 377 :347-355
[9]   VOLUME CHANGES IN LIVER MITOCHONDRIA [J].
AZZONE, GF ;
AZZI, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1965, 53 (05) :1084-&
[10]   Loss of cyclophilin D reveals a critical role for mitochondrial permeability transition in cell death [J].
Baines, CP ;
Kaiser, RA ;
Purcell, NH ;
Blair, NS ;
Osinska, H ;
Hambleton, MA ;
Brunskill, EW ;
Sayen, MR ;
Gottlieb, RA ;
Dorn, GW ;
Robbins, J ;
Molkentin, JD .
NATURE, 2005, 434 (7033) :658-662