Gross I, Bassit B, Benezra M, Licht J D
Derald H. Ruttenberg Cancer Center and Department of Medicine, Box 1130, Mount Sinai School of Medicine, New York, New York 10029, USA.
J Biol Chem. 2001 Dec 7;276(49):46460-8. doi: 10.1074/jbc.M108234200. Epub 2001 Oct 3.
Sprouty was genetically identified as an antagonist of fibroblast growth factor signaling during tracheal branching in Drosophila. In this study, we provide a functional characterization of mammalian Sprouty1 and Sprouty2. Sprouty1 and Sprouty2 inhibited events downstream of multiple receptor tyrosine kinases and regulated both cell proliferation and differentiation. Using NIH3T3 cell lines conditionally expressing Sprouty1 or Sprouty2, we found that these proteins specifically inhibit the Ras/Raf/MAP kinase pathway by preventing Ras activation. In contrast, activation of the phosphatidylinositol 3-kinase pathway was not affected by Sprouty1 or Sprouty2. We further showed that Sprouty1 and Sprouty2 do no prevent the formation of a SNT.Grb2.Sos complex upon fibroblast growth factor stimulation, yet block Ras activation. Taken together, these results establish mammalian Sprouty proteins as important negative regulators of growth factor signaling and suggest that Sprouty proteins act downstream of the Grb2.Sos complex to selectively uncouple growth factor signals from Ras activation and the MAP Kinase pathway.
在果蝇气管分支过程中,Sprouty基因被确定为成纤维细胞生长因子信号的拮抗剂。在本研究中,我们对哺乳动物的Sprouty1和Sprouty2进行了功能特性分析。Sprouty1和Sprouty2抑制多种受体酪氨酸激酶下游的事件,并调节细胞增殖和分化。使用条件性表达Sprouty1或Sprouty2的NIH3T3细胞系,我们发现这些蛋白通过阻止Ras激活来特异性抑制Ras/Raf/丝裂原活化蛋白激酶(MAPK)途径。相比之下,磷脂酰肌醇3激酶途径的激活不受Sprouty1或Sprouty2的影响。我们进一步表明,Sprouty1和Sprouty2在成纤维细胞生长因子刺激时并不阻止SNT.Grb2.Sos复合物的形成,但会阻断Ras激活。综上所述,这些结果确立了哺乳动物Sprouty蛋白作为生长因子信号重要负调节因子的地位,并表明Sprouty蛋白在Grb2.Sos复合物下游起作用,以选择性地使生长因子信号与Ras激活和MAPK途径解偶联。