Fanger G R, Gerwins P, Widmann C, Jarpe M B, Johnson G L
Program in Molecular Signal Transduction Division of Basic Sciences National Jewish Center for Immunology and Respiratory Medicine 1400 Jackson Street Denver Colorado 80206 USA.
Curr Opin Genet Dev. 1997 Feb;7(1):67-74. doi: 10.1016/s0959-437x(97)80111-6.
Regulation of the mitogen-activated protein kinase (MAPK) family members - which include the extracellular response kinases (ERKs), p38/HOG1, and the c-Jun amino-terminal kinases (JNKs) - plays a central role in mediating the effects of diverse stimuli encompassing cytokines, hormones, growth factors and stresses such as osmotic imbalance, heat shock, inhibition of protein synthesis and irradiation. A rapidly increasing number of kinases that activate the JNK pathways has been described recently, including the MAPK/ERK kinase kinases, p21-activated kinases, germinal center kinase, mixed lineage kinases, tumor progression locus 2, and TGF-beta-activated kinase. Thus, regulation of the JNK pathway provides an interesting example of how many different stimuli can converge into regulating pathways critical for the determination of cell fate.
丝裂原活化蛋白激酶(MAPK)家族成员——包括细胞外信号调节激酶(ERK)、p38/HOG1和c-Jun氨基末端激酶(JNK)——的调节在介导多种刺激的作用中发挥核心作用,这些刺激包括细胞因子、激素、生长因子以及诸如渗透压失衡、热休克、蛋白质合成抑制和辐射等应激。最近已经描述了越来越多激活JNK途径的激酶,包括MAPK/ERK激酶激酶、p21活化激酶、生发中心激酶、混合谱系激酶、肿瘤进展位点2和TGF-β活化激酶。因此,JNK途径的调节提供了一个有趣的例子,说明许多不同的刺激如何汇聚到对细胞命运决定至关重要的调节途径中。