Mitochondrial cell death effectors

被引:367
作者
Brenner, Dirk [1 ]
Mak, Tak W. [1 ,2 ,3 ]
机构
[1] Univ Hlth Network, Campbell Family Canc Res Inst, Ontario Canc Inst, Toronto, ON M5G 2C1, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON M5G 2M9, Canada
基金
加拿大健康研究院;
关键词
CYTOCHROME-C RELEASE; BCL-X-L; MEMBRANE PERMEABILIZATION; BH3-ONLY PROTEINS; INDUCED APOPTOSIS; DEFICIENT MICE; BH3; DOMAINS; BAX; REQUIREMENT; INHIBITION;
D O I
10.1016/j.ceb.2009.09.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Programmed cell death (apoptosis) is crucial for embryogenesis and tissue homeostasis. Deregulated apoptosis leads to immunodeficiency, autoimmune disorders or cancer. The two main routes to apoptosis are the extrinsic and intrinsic (mitochondrial) pathways. Both involve caspase activation that leads to the cleavage of multiple intracellular substrates [1,9]. This review highlights recent advances in our understanding of the intrinsic pathway. We describe how BCL-2-family members preserve or disrupt mitochondrial integrity, the contribution of BH3-only proteins to this process, and the importance of cytotoxic factors released by the mitochondria. The growing evidence that the intrinsic pathway is crucial for tumourigenesis makes this an intriguing field. In particular, the finding that BCL-2 homologues are inhibited by BH3-only proteins may have future therapeutic applications.
引用
收藏
页码:871 / 877
页数:7
相关论文
共 60 条
[1]   A cytochrome c mutant with high electron transfer and antioxidant activities but devoid of apoptogenic effect [J].
Abdullaev, ZK ;
Bodrova, ME ;
Chernyak, BV ;
Dolgikh, DA ;
Kluck, RM ;
Perverzev, MO ;
Arseniev, AS ;
Efremov, RG ;
Kirpichnikov, MP ;
Mokhova, EN ;
Newmeyer, DD ;
Roder, H ;
Skulachev, VP .
BIOCHEMICAL JOURNAL, 2002, 362 :749-754
[2]   Anti-apoptotic oncogenes prevent caspase-dependent and independent commitment for cell death [J].
Amarante-Mendes, GP ;
Finucane, DM ;
Martin, SJ ;
Cotter, TG ;
Salvesen, GS ;
Green, DR .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (04) :298-306
[3]   Bax-type apoptotic proteins porate pure lipid bilayers through a mechanism sensitive to intrinsic monolayer curvature [J].
Basañez, G ;
Sharpe, JC ;
Galanis, J ;
Brandt, TB ;
Hardwick, JM ;
Zimmerberg, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (51) :49360-49365
[4]   Differential targeting of prosurvival Bcl-2 proteins by their BH3-only ligands allows complementary apoptotic function [J].
Chen, L ;
Willis, SN ;
Wei, A ;
Smith, BJ ;
Fletcher, JI ;
Hinds, MG ;
Colman, PM ;
Day, CL ;
Adams, JM ;
Huang, DCS .
MOLECULAR CELL, 2005, 17 (03) :393-403
[5]   BCL-2, BCL-XL sequester BH3 domain-only molecules preventing BAX- and BAK-mediated mitochondrial apoptosis [J].
Cheng, EHYA ;
Wei, MC ;
Weiler, S ;
Flavell, RA ;
Mak, TW ;
Lindsten, T ;
Korsmeyer, SJ .
MOLECULAR CELL, 2001, 8 (03) :705-711
[6]   Mechanism of apoptosis induction by inhibition of the anti-apoptotic BCL-2 proteins [J].
Chipuk, Jerry E. ;
Fisher, John C. ;
Dillon, Christopher P. ;
Kriwacki, Richard W. ;
Kuwana, Tomomi ;
Green, Douglas R. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (51) :20327-20332
[7]   GAPDH and autophagy preserve survival after apoptotic cytochrome c release in the absence of caspase activation [J].
Colell, Anna ;
Ricci, Jean-Ehrland ;
Tait, Stephen ;
Milasta, Sandra ;
Maurer, Ulrich ;
Bouchier-Hayes, Lisa ;
Fitzgerald, Patrick ;
Guio-Carrion, Ana ;
Waterhouse, Nigel J. ;
Li, Cindy Wei ;
Mari, Bernard ;
Barbry, Pascal ;
Newmeyer, Donald D. ;
Beere, Helen M. ;
Green, Douglas R. .
CELL, 2007, 129 (05) :983-997
[8]   Cell death: Critical control points [J].
Danial, NN ;
Korsmeyer, SJ .
CELL, 2004, 116 (02) :205-219
[9]   Apaf-1 and caspase-9 accelerate apoptosis, but do not determine whether factor-deprived or drug-treated cells die [J].
Ekert, PG ;
Read, SH ;
Silke, J ;
Marsden, VS ;
Kaufmann, H ;
Hawkins, CJ ;
Gerl, R ;
Kumar, S ;
Vaux, DL .
JOURNAL OF CELL BIOLOGY, 2004, 165 (06) :835-842
[10]   Smac agonists sensitize for Apo2L/TRAIL- or anticancer drug-induced apoptosis and induce regression of malignant glioma in vivo [J].
Fulda, S ;
Wick, W ;
Weller, M ;
Debatin, KM .
NATURE MEDICINE, 2002, 8 (08) :808-815