Induction of apoptosis by ASK1, a mammalian MAPKKK that activates SAPK/JNK and p38 signaling pathways

被引:2029
作者
Ichijo, H
Nishida, E
Irie, K
tenDijke, P
Saitoh, M
Moriguchi, T
Takagi, M
Matsumoto, K
Miyazono, K
Gotoh, Y
机构
[1] KYOTO UNIV,INST VIRUS RES,DEPT GENET & MOL BIOL,SAKYO KU,KYOTO 60601,JAPAN
[2] NAGOYA UNIV,FAC SCI,DEPT MOL BIOL,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
[3] BIOMED CTR,LUDWIG INST CANC RES,S-75124 UPPSALA,SWEDEN
[4] TOKYO MED & DENT UNIV,DEPT ORAL PATHOL,BUNKYO KU,TOKYO 113,JAPAN
关键词
D O I
10.1126/science.275.5296.90
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mitogen-activated protein (MAP) kinase cascades are activated in response to various extracellular stimuli, including growth factors and environmental stresses. A MAP kinase kinase kinase (MAPKKK), termed ASK1, was identified that activated two different subgroups of MAP kinase kinases (MAPKK), SEK1 (or MKK4) and MKK3/MAPKK6 (or MKK6), which in turn activated stress-activated protein kinase (SAPK, also known as JNK; c-Jun amino-terminal kinase) and p38 subgroups of MAP kinases, respectively. Overexpression of ASK1 induced apoptotic cell death, and ASK1 was activated in cells treated with tumor necrosis factor-alpha (TNF-alpha), Moreover, TNF-alpha-induced apoptosis was inhibited by a catalytically inactive form of ASK1. ASK1 may be a key element in the mechanism of stress- and cytokine-induced apoptosis.
引用
收藏
页码:90 / 94
页数:5
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