Yenush L, White M F
Research Division, Joslin Diabetes Center, Boston, MA, USA.
Bioessays. 1997 Jun;19(6):491-500. doi: 10.1002/bies.950190608.
The discovery of the first intracellular substrate for insulin, IRS-1, redirected the field of diabetes research and has led to many important advances in our understanding of insulin action. Detailed analysis of IRS-1 demonstrates structure/function relationships for this modular docking molecule, including mechanisms of substrate recognition and signal propagation. Recent work has also identified other structurally similar molecules, including IRS-2, the Drosophila protein, DOS, and the Grb2-binding protein, Gab1, suggesting that this intracellular signalling strategy is conserved evolutionarily and is utilized by an expanding number of receptor systems. In fact, IRS-1 itself has been shown to be important in other growth factor and cytokine signalling systems, including growth hormone and several interleukins. Analysis of mice lacking IRS-1 confirms an important physiological role for this protein in glucose metabolism and general cell growth in the intact animal. Disregulation of the signalling pathways integrated by the IRS proteins may contribute to the pathophysiology of non-insulin-dependent diabetes mellitus or other diseases.
胰岛素首个细胞内底物 IRS-1 的发现,使糖尿病研究领域重新定向,并在我们对胰岛素作用的理解上带来了许多重要进展。对 IRS-1 的详细分析揭示了这种模块化对接分子的结构/功能关系,包括底物识别和信号传导机制。最近的研究还鉴定出了其他结构相似的分子,包括 IRS-2、果蝇蛋白 DOS 以及 Grb2 结合蛋白 Gab1,这表明这种细胞内信号传导策略在进化上是保守的,并且被越来越多的受体系统所利用。事实上,IRS-1 本身已被证明在其他生长因子和细胞因子信号传导系统中也很重要,包括生长激素和几种白细胞介素。对缺乏 IRS-1 的小鼠的分析证实了该蛋白在完整动物的葡萄糖代谢和一般细胞生长中具有重要的生理作用。由 IRS 蛋白整合的信号通路失调可能导致非胰岛素依赖型糖尿病或其他疾病的病理生理学。