Marshall C J
Chester Beatty Laboratories, Institute of Cancer Research, London, England.
Cell. 1995 Jan 27;80(2):179-85. doi: 10.1016/0092-8674(95)90401-8.
A number of different intracellular signaling pathways have been shown to be activated by receptor tyrosine kinases. These activation events include the phosphoinositide 3-kinase, 70 kDa S6 kinase, mitogen-activated protein kinase (MAPK), phospholipase C-gamma, and the Jak/STAT pathways. The precise role of each of these pathways in cell signaling remains to be resolved, but studies on the differentiation of mammalian PC12 cells in tissue culture and the genetics of cell fate determination in Drosophila and Caenorhabditis suggest that the extracellular signal-regulated kinase (ERK-regulated) MAPK pathway may be sufficient for these cellular responses. Experiments with PC12 cells also suggest that the duration of ERK activation is critical for cell signaling decisions.
已证明多种不同的细胞内信号通路可被受体酪氨酸激酶激活。这些激活事件包括磷酸肌醇3激酶、70 kDa S6激酶、丝裂原活化蛋白激酶(MAPK)、磷脂酶C-γ以及Jak/STAT通路。这些通路中每一条在细胞信号传导中的精确作用仍有待确定,但对组织培养中哺乳动物PC12细胞分化以及果蝇和秀丽隐杆线虫细胞命运决定遗传学的研究表明,细胞外信号调节激酶(ERK调节的)MAPK通路可能足以引发这些细胞反应。对PC12细胞的实验还表明,ERK激活的持续时间对细胞信号传导决策至关重要。