Ceresa B P, Pessin J E
Department of Physiology and Biophysics, The University of Iowa, Iowa City 52242, USA.
Mol Cell Biochem. 1998 May;182(1-2):23-9.
In addition to mediating a number of metabolic functions, insulin also uses mitogenic pathways to maintain cellular homeostasis. Many of these mitogenic responses are mediated by signals through the small molecular weight guanine nucleotide binding protein, Ras. In the last decade, great progress has been made in understanding the molecular mechanisms which regulate the insulin mediated conversion of Ras from its inactive, GDP-bound state, to the activated GTP-bound form. More recently, it has been appreciated that insulin also regulates the inactivation of this pathway, namely by uncoupling the protein complexes whose formation is required for Ras activation. This review addresses molecular mechanism which both positively and negatively regulate this mitogenic signalling pathway.
除了介导多种代谢功能外,胰岛素还利用促有丝分裂途径来维持细胞内稳态。许多这些促有丝分裂反应是由通过小分子量鸟嘌呤核苷酸结合蛋白Ras的信号介导的。在过去十年中,在理解调节胰岛素介导的Ras从无活性的GDP结合状态转变为活化的GTP结合形式的分子机制方面取得了巨大进展。最近,人们认识到胰岛素还调节该途径的失活,即通过解开Ras激活所需形成的蛋白质复合物。这篇综述探讨了正向和负向调节这种促有丝分裂信号通路的分子机制。