Bax is present as a high molecular weight oligomer/complex in the mitochondrial membrane of apoptotic cells

被引:588
作者
Antonsson, B [1 ]
Montessuit, S [1 ]
Sanchez, B [1 ]
Martinou, JC [1 ]
机构
[1] Serono Int SA, Serono Pharmaceut Res Inst, CH-1228 Geneva, Switzerland
关键词
D O I
10.1074/jbc.M010810200
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
Bax is a Bcl-2 family protein with proapoptotic activity, which has been shown to trigger cytochrome c release from mitochondria both in vitro and in vivo. In control HeLa cells, Bax is present in the cytosol and weakly associated with mitochondria as a monomer with an apparent molecular mass of 20,000 Da. After treatment of the HeLa cells with the apoptosis inducer staurosporine or UV irradiation, Bax associated with mitochondria is present as two large molecular weight oligomers/complexes of 96,000 and 260,000 Da, which are integrated into the mitochondrial membrane. Bcl-2 prevents Bax oligomerization and insertion into the mitochondrial membrane. The outer mitochondrial membrane protein voltage-dependent anion channel and the inner mitochondrial membrane protein adenosine nucleotide translocator do not coelute with the large molecular weight Bax oligomers/complexes on gel filtration. Bax oligomerization appears to be required for its proapoptotic activity, and the Bax oligomer/complex might constitute the structural entirety of the cytochrome c-conducting channel in the outer mitochondrial membrane.
引用
收藏
页码:11615 / 11623
页数:9
相关论文
共 64 条
[1]   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
[2]   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
[3]   THE PROTEIN BCL-2-ALPHA DOES NOT REQUIRE MEMBRANE ATTACHMENT, BUT 2 CONSERVED DOMAINS TO SUPPRESS APOPTOSIS [J].
BORNER, C ;
MARTINOU, I ;
MATTMANN, C ;
IRMLER, M ;
SCHAERER, E ;
MARTINOU, JC ;
TSCHOPP, J .
JOURNAL OF CELL BIOLOGY, 1994, 126 (04) :1059-1068
[4]   Mitochondrial cytochrome c release in apoptosis occurs upstream of DEVD-specific caspase activation and independently of mitochondrial transmembrane depolarization [J].
Bossy-Wetzel, E ;
Newmeyer, DD ;
Green, DR .
EMBO JOURNAL, 1998, 17 (01) :37-49
[5]  
CHITTENDEN T, 1995, EMBO J, V14, P733
[6]   Solution structure of BID, an intracellular amplifier of apoptotic signaling [J].
Chou, JJ ;
Li, HL ;
Salvesen, GS ;
Yuan, JY ;
Wagner, G .
CELL, 1999, 96 (05) :615-624
[7]   Bcl-2 is a monomeric protein:: prevention of homodimerization by structural constraints [J].
Conus, S ;
Kaufmann, T ;
Fellay, I ;
Otter, I ;
Rossé, T ;
Borner, C .
EMBO JOURNAL, 2000, 19 (07) :1534-1544
[8]   Cyclophilin-D binds strongly to complexes of the voltage-dependent anion channel and the adenine nucleotide translocase to form the permeability transition pore [J].
Crompton, M ;
Virji, S ;
Ward, JM .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 258 (02) :729-735
[9]   Bid-induced conformational change of Bax is responsible for mitochondrial cytochrome c release during apoptosis [J].
Desagher, S ;
Osen-Sand, A ;
Nichols, A ;
Eskes, R ;
Montessuit, S ;
Lauper, S ;
Maundrell, K ;
Antonsson, B ;
Martinou, JC .
JOURNAL OF CELL BIOLOGY, 1999, 144 (05) :891-901
[10]   Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition [J].
Du, CY ;
Fang, M ;
Li, YC ;
Li, L ;
Wang, XD .
CELL, 2000, 102 (01) :33-42