ASC is a Bax adaptor and regulates the p53-Bax mitochondrial apoptosis pathway

被引:211
作者
Ohtsuka, T
Ryu, H
Minamishima, YA
Macip, S
Sagara, J
Nakayama, KI
Aaronson, SA
Lee, SW [1 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Canc Biol Program, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Boston Univ, Sch Med, Dept Neurol, Ctr Geriatr Res Educ & Clin, Bedford, MA 01730 USA
[4] Mt Sinai Sch Med, Derald H Ruttenberg Canc Ctr, New York, NY 10029 USA
[5] Shinshu Univ, Sch Med, Dept Mol Oncol & Angiol, Nagano 3908621, Japan
[6] Kyushu Univ, Med Inst Bioregulat, Dept Mol Biol, Higashi Ku, Fukuoka 8128582, Japan
[7] Kyushu Univ, Med Inst Bioregulat, Dept Cellular Biol, Higashi Ku, Fukuoka 8128582, Japan
关键词
D O I
10.1038/ncb1087
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The apoptosis-associated speck-like protein (ASC) is an unusual adaptor protein that contains the Pyrin/PAAD death domain in addition to the CARD protein-protein interaction domain(1-5). Here, we present evidence that ASC can function as an adaptor molecule for Bax and regulate a p53-Bax mitochondrial pathway of apoptosis. When ectopically expressed, ASC interacted directly with Bax, colocalized with Bax to the mitochondria, induced cytochrome c release with a significant reduction of mitochondrial membrane potential and resulted in the activation of caspase-9, -2 and -3. The rapid induction of apoptosis by ASC was not observed in Bax-deficient cells. We also show that induction of ASC after exposure to genotoxic stress is dependent on p53. Blocking of endogenous ASC expression by small-interfering RNA ( siRNA) reduced the apoptotic response and inhibited translocation of Bax to mitochondria in response to p53 or genotoxic insult, suggesting that ASC is required to translocate Bax to the mitochondria. Our findings demonstrate that ASC has an essential role in the intrinsic mitochondrial pathway of apoptosis through a p53-Bax network.
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页码:121 / +
页数:11
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