Shi Yu, Gaestel Matthias
Hannover Medical School, Institute of Biochemistry, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.
Biol Chem. 2002 Oct;383(10):1519-36. doi: 10.1515/BC.2002.173.
Mitogen-activated protein kinases (MAPKs) are evolutionarily conserved enzymes which connect cell-surface receptors to regulatory targets within cells and convert receptor signals into various outputs. In mammalian cells, four distinct MAPKs have been identified: the extracellular signal-related kinases (ERK)-1/2, the c-jun N-terminal kinases or stress-activated protein kinases 1 (JNK1/2/3, or SAPK1s), the p38 MAPKs (p38 alpha/beta/gamma/delta, or SAPK2s), and the ERK5 or big MAP kinase 1 (BMK1). The p38 MAPK cascade is activated by stress or cytokines and leads to phosphorylation of its central elements, the p38 MAPKs. Downstream of p38 MAPKs there is a diversification and extensive branching of signalling pathways. For that reason, we will focus in this review on the different signalling events that are triggered by p38 activity, and analyse how these events contribute to specific gene expression and cellular responses.
丝裂原活化蛋白激酶(MAPKs)是进化上保守的酶,它们将细胞表面受体与细胞内的调节靶点连接起来,并将受体信号转化为各种输出。在哺乳动物细胞中,已鉴定出四种不同的MAPKs:细胞外信号调节激酶(ERK)-1/2、c-jun氨基末端激酶或应激激活蛋白激酶1(JNK1/2/3,或SAPK1s)、p38 MAPKs(p38α/β/γ/δ,或SAPK2s)以及ERK5或大MAP激酶1(BMK1)。p38 MAPK级联由应激或细胞因子激活,并导致其核心元件p38 MAPKs的磷酸化。在p38 MAPKs的下游,信号通路存在多样化和广泛的分支。因此,在本综述中,我们将重点关注由p38活性触发的不同信号事件,并分析这些事件如何促成特定基因表达和细胞反应。