Carraway K L, Carraway C A
Department of Cell Biology and Anatomy, University of Miami School of Medicine, FL 33101.
Bioessays. 1995 Feb;17(2):171-5. doi: 10.1002/bies.950170212.
Stimulation of mitogenesis by the epidermal growth factor (EGF) operates through a pathway involving the receptor, the small G-protein Ras and protein kinases of the MAP kinase cascade. It is proposed that two of the critical steps of that pathway utilize localization of components to the plasma membrane where Ras is located: recruitment of the nucleotide exchange protein Sos to the phosphorylated EGF receptor via a complex with the SH2/SH3-containing protein Grb2 and recruitment of the protein kinase Raf to activated Ras. Moreover, it is then proposed that Raf associates with the cytoskeleton at the membrane as it is being activated. Other signaling elements, including class I receptor kinases, nonreceptor tyrosine kinases and tyrosine phosphatases, are known to function at specific cellular sites. These observations have led us to propose that localization of signaling components, and particularly sites at membrane-microfilament interfaces, play critical roles in cellular regulation.
表皮生长因子(EGF)刺激有丝分裂是通过一条涉及受体、小G蛋白Ras和丝裂原活化蛋白激酶(MAP激酶)级联反应中的蛋白激酶的信号通路来实现的。有人提出,该信号通路中的两个关键步骤利用了组分定位于Ras所在的质膜这一特性:通过与含SH2/SH3结构域的蛋白Grb2形成复合物,将核苷酸交换蛋白Sos招募到磷酸化的EGF受体上,以及将蛋白激酶Raf招募到活化的Ras上。此外,有人还提出,Raf在被激活时会与膜上的细胞骨架结合。已知其他信号元件,包括I类受体激酶、非受体酪氨酸激酶和酪氨酸磷酸酶,在特定的细胞位点发挥作用。这些观察结果使我们提出,信号组分的定位,特别是膜-微丝界面处的位点,在细胞调节中起着关键作用。