Ichijo H, Nishida E, Irie K, ten Dijke P, Saitoh M, Moriguchi T, Takagi M, Matsumoto K, Miyazono K, Gotoh Y
Department of Biochemistry, The Cancer Institute, Tokyo, Japanese Foundation for Cancer Research, 1-37-1 Kami-Ikebukuro, Toshima-ku, Tokyo 170, Japan.
Science. 1997 Jan 3;275(5296):90-4. doi: 10.1126/science.275.5296.90.
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.
丝裂原活化蛋白(MAP)激酶级联反应在响应各种细胞外刺激时被激活,这些刺激包括生长因子和环境压力。一种名为ASK1的丝裂原活化蛋白激酶激酶激酶(MAPKKK)被鉴定出来,它可激活丝裂原活化蛋白激酶激酶(MAPKK)的两个不同亚组,即SEK1(或MKK4)和MKK3/MAPKK6(或MKK6),而这两个亚组又分别激活应激激活蛋白激酶(SAPK,也称为JNK;c-Jun氨基末端激酶)和MAP激酶的p38亚组。ASK1的过表达诱导细胞凋亡性死亡,并且ASK1在经肿瘤坏死因子-α(TNF-α)处理的细胞中被激活。此外,ASK1的催化失活形式可抑制TNF-α诱导的细胞凋亡。ASK1可能是应激和细胞因子诱导的细胞凋亡机制中的关键元件。