The IRS-signalling system: A network of docking proteins that mediate insulin action

被引:583
作者
White, MF
机构
[1] Harvard Univ, Sch Med, Joslin Diabet Ctr, Div Res, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Grad Program Biomed & Biol Sci, Boston, MA 02115 USA
关键词
IRS-1; proteins; PI-3; kinase; Ras-MAP kinase; SHP2; diabetes;
D O I
10.1023/A:1006806722619
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
New molecules discovered during the past ten years have created a rational framework to understand signalling transduction by a broad range of growth factors and cytokines, including insulin. Insulin action is initiated through the insulin receptor, a transmembrane glycoprotein with intrinsic protein tyrosine kinase activity. The tyrosine kinase mediates the insulin response through tyrosine phosphorylation of various cellular substrates, in particular the IRS-proteins. During insulin-stimulated tyrosine phosphorylation, the IRS-proteins mediate a broad biological response by binding and activating various enzymes or adapter molecules. Although we are far from a complete understanding of the insulin signalling system and its failure, enough pieces of the puzzle are falling into place that mechanism-based solutions to insulin resistance encountered with type II diabetes may soon be attainable.
引用
收藏
页码:3 / 11
页数:9
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