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凋亡信号调节激酶1(ASK1)是角质形成细胞分化的细胞内诱导剂。

Apoptosis signal-regulating kinase 1 (ASK1) is an intracellular inducer of keratinocyte differentiation.

作者信息

Sayama K, Hanakawa Y, Shirakata Y, Yamasaki K, Sawada Y, Sun L, Yamanishi K, Ichijo H, Hashimoto K

机构信息

Department of Dermatology, Ehime University School of Medicine, Ehime 791-0295, Japan.

出版信息

J Biol Chem. 2001 Jan 12;276(2):999-1004. doi: 10.1074/jbc.M003425200.

Abstract

Cells differentiate in response to various extracellular stimuli. This cellular response requires intracellular signaling pathways. The mitogen-activated protein (MAP) kinase cascade is a core signal transduction pathway that determines the fate of many kinds of cell. MAP kinase kinase kinase activates MAP kinase kinase, which in turn activates MAP kinase. Apoptosis signal-regulating kinase (ASK1) was identified as a MAP kinase kinase kinase involved in the stress-induced apoptosis-signaling cascade that activates the SEK1-JNK and MKK3/MKK6-p38 MAP kinase cascades. Expression of the constitutively active form of ASK1 (ASK1-DeltaN) in keratinocytes induced significant morphological changes and differentiation markers, transglutaminase-1, loricrin, and involucrin. A transient increase in p21(Cip1/WAF1) reduced DNA synthesis, and cell cycle analysis verified the differentiation. p38 MAP kinase inhibitors, SB202190 and SB203580, abolished the induction of differentiation markers, transglutaminase-1, loricrin, and involucrin. In turn, the induction of differentiation with ceramide in keratinocytes caused an increase in ASK1 expression and activity. Furthermore, normal human skin expresses ASK1 protein in the upper epidermis, implicating ASK1 in in vivo keratinocyte differentiation. We propose that the ASK1-p38 MAP kinase cascade is a new intracellular regulator of keratinocyte differentiation.

摘要

细胞会对各种细胞外刺激做出分化反应。这种细胞反应需要细胞内信号通路。丝裂原活化蛋白(MAP)激酶级联反应是一种核心信号转导通路,它决定了多种细胞的命运。MAP激酶激酶激酶激活MAP激酶激酶,而MAP激酶激酶又激活MAP激酶。凋亡信号调节激酶(ASK1)被鉴定为一种MAP激酶激酶激酶,参与应激诱导的凋亡信号级联反应,该反应激活SEK1-JNK和MKK3/MKK6-p38 MAP激酶级联反应。在角质形成细胞中表达组成型活性形式的ASK1(ASK1-DeltaN)会诱导显著的形态变化和分化标志物,如转谷氨酰胺酶-1、兜甲蛋白和内披蛋白。p21(Cip1/WAF1)的短暂增加会减少DNA合成,细胞周期分析证实了分化。p38 MAP激酶抑制剂SB202190和SB203580消除了分化标志物转谷氨酰胺酶-1、兜甲蛋白和内披蛋白的诱导。反过来,角质形成细胞中神经酰胺诱导的分化会导致ASK1表达和活性增加。此外,正常人类皮肤在上层表皮中表达ASK1蛋白,这表明ASK1参与体内角质形成细胞的分化。我们提出ASK1-p38 MAP激酶级联反应是角质形成细胞分化的一种新的细胞内调节因子。

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