The still uncertain identity of the channel-forming unit(s) of the mitochondrial permeability transition pore

被引:59
作者
Baines, Christopher P. [1 ,2 ,3 ]
Gutierrez-Aguilar, Manuel [4 ]
机构
[1] Univ Missouri, Dalton Cardiovasc Res Ctr, Res Pk Dr, Columbia, MO 65211 USA
[2] Univ Missouri, Dept Biomed Sci, Columbia, MO 65211 USA
[3] Univ Missouri, Dept Med Pharmacol & Physiol, Columbia, MO 65211 USA
[4] Univ Nacl Autonoma Mexico, Fac Quim, Dept Bioquim, Ciudad Univ, Ciudad De Mexico 04510, Mexico
基金
美国国家卫生研究院;
关键词
Mitochondrial permeability transition pore; Phosphate carrier; ATP synthase; Adenine nucleotide translocase; Cyclophilin D; Bioenergetics; Cell death; Cyclosporin A; ADENINE-NUCLEOTIDE TRANSLOCASE; CA-2&-INDUCED MEMBRANE TRANSITION; DEPENDENT ANION CHANNEL; CRITICAL THIOL-GROUPS; CYCLOPHILIN-D; ATP SYNTHASE; CYCLOSPORINE-A; PHOSPHATE CARRIER; N-ETHYLMALEIMIDE; INORGANIC-PHOSPHATE;
D O I
10.1016/j.ceca.2018.05.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondria from different organisms can undergo a sudden process of inner membrane unselective leakiness to molecules known as the mitochondrial permeability transition (MPT). This process has been studied for nearly four decades and several proteins have been claimed to constitute, or at least regulate the usually inactive pore responsible for this transition. However, no protein candidate proposed as the actual pore-forming unit has passed rigorous gain- or loss-of-function genetic tests. Here we review evidence for - and against-putative channel-forming components of the MPT pore. We conclude that the structure of the MPT pore still remains largely undefined and suggest that future studies should follow established technical considerations to unambiguously consolidate the channel forming constituent(s) of the MPT pore.
引用
收藏
页码:121 / 130
页数:10
相关论文
共 104 条
[1]   An uncoupling channel within the c-subunit ring of the F1FO ATP synthase is the mitochondrial permeability transition pore [J].
Alavian, Kambiz N. ;
Beutner, Gisela ;
Lazrove, Emma ;
Sacchetti, Silvio ;
Park, Han-A ;
Licznerski, Pawel ;
Li, Hongmei ;
Nabili, Panah ;
Hockensmith, Kathryn ;
Graham, Morven ;
Porter, George A., Jr. ;
Jonas, Elizabeth A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (29) :10580-10585
[2]  
Alcala S., 2007, ONCOGENE, V27
[3]  
Altschuld R.A., 1992, AM J PHYSIOL, V262, P704
[4]   Mitochondrial Ca2+ transport and permeability transition in zebrafish (Danio rerio) [J].
Azzolin, Luca ;
Basso, Emy ;
Argenton, Francesco ;
Bernardi, Paolo .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2010, 1797 (11) :1775-1779
[5]   Adenine nucleotide translocase-1 induces cardiomyocyte death through upregulation of the pro-apoptotic protein Bax [J].
Baines, Christopher P. ;
Molkentin, Jeffery D. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2009, 46 (06) :969-977
[6]   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
[7]   Phosphate is essential for inhibition of the mitochondrial permeability transition pore by cyclosporin A and by cyclophilin D ablation [J].
Basso, Emy ;
Petronilli, Valeria ;
Forte, Michael A. ;
Bernardi, Paolo .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (39) :26307-26311
[8]   Commentary: The m-AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria [J].
Bernardi, Paolo ;
Forte, Michael .
FRONTIERS IN PHYSIOLOGY, 2016, 7
[9]   Cyclophilin D regulates the dynamic assembly of mitochondrial ATP synthase into synthasomes [J].
Beutner, Gisela ;
Alanzalon, Ryan E. ;
Porter, George A., Jr. .
SCIENTIFIC REPORTS, 2017, 7
[10]   The mitochondrial permeability transition pore in AD 2016: An update [J].
Biasutto, Lucia ;
Azzolini, Michele ;
Szabo, Ildiko ;
Zoratti, Mario .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2016, 1863 (10) :2515-2530