Cardiolipin provides an essential activating platform for caspase-8 on mitochondria

被引:228
作者
Gonzalvez, Francois [1 ]
Schug, Zachary T. [1 ]
Houtkooper, Riekelt H. [2 ,3 ]
MacKenzie, Elaine D. [1 ]
Brooks, David G. [4 ]
Wanders, Ronald J. A. [2 ,3 ]
Petit, Patrice X. [5 ,6 ]
Vaz, Frederic M. [2 ,3 ]
Gottlieb, Eyal [1 ]
机构
[1] Beatson Inst Canc Res, Canc Res UK, Glasgow G61 1BD, Lanark, Scotland
[2] Univ Amsterdam, Acad Med Ctr, Lab Genet Metab Dis, Dept Clin Chem, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Lab Genet Metab Dis, Dept Pediat, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Penn, Dept Med, Div Med Genet, Philadelphia, PA 19104 USA
[5] INSERM, CNRS, UMR 8104, Dept Genet & Dev,Inst Cochin,U567, F-75014 Paris, France
[6] Univ Paris 05, F-75014 Paris, France
关键词
D O I
10.1083/jcb.200803129
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cardiolipin is a mitochondria-specific phospholipid known to be intimately involved with apoptosis. However, the lack of appropriate cellular models to date restricted analysis of its role in cell death. The maturation of cardiolipin requires the transacylase tafazzin, which is mutated in the human disorder Barth syndrome. Using Barth syndrome patient-derived cells and HeLa cells in which tafazzin was knocked down, we show that cardiolipin is required for apoptosis in the type II mitochondria-dependent response to Fas stimulation. Cardiolipin provides an anchor and activating platform for caspase-8 translocation to, and embedding in, the mitochondrial membrane, where it oligomerizes and is further activated, steps that are necessary for an efficient type II apoptotic response.
引用
收藏
页码:681 / 696
页数:16
相关论文
共 52 条
[1]  
ARDAIL D, 1990, J BIOL CHEM, V265, P18797
[2]   AN X-LINKED MITOCHONDRIAL DISEASE AFFECTING CARDIAC-MUSCLE, SKELETAL-MUSCLE AND NEUTROPHIL LEUKOCYTES [J].
BARTH, PG ;
SCHOLTE, HR ;
BERDEN, JA ;
VANDERKLEIVANMOORSEL, JM ;
LUYTHOUWEN, IEM ;
VANTVEERKORTHOF, ET ;
VANDERHARTEN, JJ ;
SOBOTKAPLOJHAR, MA .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1983, 62 (1-3) :327-355
[3]   A novel X-linked gene, G4.5. is responsible for Barth syndrome [J].
Bione, S ;
DAdamo, P ;
Maestrini, E ;
Gedeon, AK ;
Bolhuis, PA ;
Toniolo, D .
NATURE GENETICS, 1996, 12 (04) :385-389
[4]   Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth Syndrome [J].
Bleyl, SB ;
Mumford, BR ;
Thompson, V ;
Carey, JC ;
Pysher, TJ ;
Chin, TK ;
Ward, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) :868-872
[5]   Association of active caspase 8 with the mitochondrial membrane during apoptosis: Potential roles in cleaving BAP31 and caspase 3 and mediating mitochondrion-endoplasmic reticulum cross talk in etoposide-induced cell death [J].
Chandra, D ;
Choy, G ;
Deng, XD ;
Bhatia, B ;
Daniel, P ;
Tang, DG .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (15) :6592-6607
[6]   Interdimer processing mechanism of procaspase-8 activation [J].
Chang, DW ;
Xing, Z ;
Capacio, VL ;
Peter, ME ;
Yang, XL .
EMBO JOURNAL, 2003, 22 (16) :4132-4142
[7]   Activation of initiator caspases through a stable dimeric intermediate [J].
Chen, M ;
Orozco, A ;
Spencer, DM ;
Wang, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (52) :50761-50767
[8]   Cardiolipin deficiency releases cytochrome c from the inner mitochondrial membrane and accelerates stimuli-elicited apoptosis [J].
Choi, S-Y ;
Gonzalvez, F. ;
Jenkins, G. M. ;
Slomianny, C. ;
Chretien, D. ;
Arnoult, D. ;
Petit, P. X. ;
Frohman, M. A. .
CELL DEATH AND DIFFERENTIATION, 2007, 14 (03) :597-606
[9]   Insights into the regulatory mechanism for caspase-8 activation [J].
Donepudi, M ;
Mac Sweeney, A ;
Briand, C ;
Grütter, MG .
MOLECULAR CELL, 2003, 11 (02) :543-549
[10]   Proapoptotic Bid binds to monolysocardiolipin, a new molecular connection between mitochondrial membranes and cell death [J].
Esposti, MD ;
Cristea, IM ;
Gaskell, SJ ;
Nakao, Y ;
Dive, C .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (12) :1300-1309