Mitochondrial regulation of apoptotic cell death

被引:105
作者
Gogvadze, Vladimir [1 ]
Orrenius, Sten [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, Div Toxicol, SE-17177 Stockholm, Sweden
关键词
mitochondria; apoptosis; cytochrome c; cardiolipin;
D O I
10.1016/j.cbi.2006.04.010
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
Mitochondria play a decisive role in the regulation of both apoptotic and necrotic cell death. Permeabilization of the outer mitochondrial membrane and subsequent release of intermembrane space proteins are important features of both models of cell death. The mechanisms by which these proteins are released depend presumably on cell type and the nature of stimuli. Of the mechanisms involved, mitochondrial permeability transition appears to be associated mainly with necrosis, whereas the release of caspase activating proteins during early apoptosis is regulated primarily by the Bcl-2 family of proteins. However, there is increasing evidence for interaction and co-operation between these two mechanisms. The multiple mechanisms of mitochondrial permeabilization may explain diversities in the response of mitochondria to numerous apoptotic stimuli in different types of cells. (c) 2006 Published by Elsevier Ireland Ltd.
引用
收藏
页码:4 / 14
页数:11
相关论文
共 98 条
[1]   THE REVERSIBLE CA-2+-INDUCED PERMEABILIZATION OF RAT-LIVER MITOCHONDRIA [J].
ALNASSER, I ;
CROMPTON, M .
BIOCHEMICAL JOURNAL, 1986, 239 (01) :19-29
[2]   Bax oligomerization is required for channel-forming activity in liposomes and to trigger cytochrome c release from mitochondria [J].
Antonsson, B ;
Montessuit, S ;
Lauper, S ;
Eskes, R ;
Martinou, JC .
BIOCHEMICAL JOURNAL, 2000, 345 :271-278
[3]   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
[4]   Implication of mitochondria-derived ROS and cardiolipin peroxiclation in N-(4-hydroxyphenyl)retinamide-induced apoptosis [J].
Asumendi, A ;
Morales, MC ;
Alvarez, A ;
Aréchaga, J ;
Pérez-Yarza, H .
BRITISH JOURNAL OF CANCER, 2002, 86 (12) :1951-1956
[5]   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
[6]   Caspases induce cytochrome c release from mitochondria by activating cytosolic factors [J].
Bossy-Wetzel, E ;
Green, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (25) :17484-17490
[7]   Pore formation and uncoupling initiate a Ca2+-independent degradation of mitochondrial phospholipids [J].
Broekemeier, KM ;
Iben, JR ;
LeVan, EG ;
Crouser, ED ;
Pfeiffer, DR .
BIOCHEMISTRY, 2002, 41 (24) :7771-7780
[8]   Inhibition of the mitochondrial permeability transition by cyclosporin a during long time frame experiments: Relationship between pore opening and the activity of mitochondrial phospholipases [J].
Broekemeier, KM ;
Pfeiffer, DR .
BIOCHEMISTRY, 1995, 34 (50) :16440-16449
[9]   Mitochondrial ADP/ATP carrier can be reversibly converted into a large channel by Ca2+ [J].
Brustovetsky, N ;
Klingenberg, M .
BIOCHEMISTRY, 1996, 35 (26) :8483-8488
[10]   Activation of calcium-independent phospholipase A2 (iPLA2) in brain mitochondria and release of apoptogenic factors by BAX and truncated BID [J].
Brustovetsky, T ;
Antonsson, B ;
Jemmerson, R ;
Dubinsky, JM ;
Brustovetsky, N .
JOURNAL OF NEUROCHEMISTRY, 2005, 94 (04) :980-994