Suppr超能文献

抑制LAR蛋白酪氨酸磷酸酶可诱导胰岛素抵抗。

Knock-down of LAR protein tyrosine phosphatase induces insulin resistance.

作者信息

Mander Ann, Hodgkinson Conrad P, Sale Graham J

机构信息

School of Biological Sciences, Biomedical Sciences Building, University of Southampton, Bassett Crescent East, Southampton, SO16 7PX, UK.

出版信息

FEBS Lett. 2005 Jun 6;579(14):3024-8. doi: 10.1016/j.febslet.2005.04.057.

Abstract

To test the role of the leukocyte common antigen-related protein tyrosine phosphatase (LAR) as a regulator of insulin receptor (IR) signalling, an siRNA probe against LAR was developed. Knock-down of LAR induced post-receptor insulin resistance with the insulin-induced activation of PKB/Akt and MAP kinases markedly inhibited. The phosphorylation and dephosphorylation of the IR and insulin receptor substrate (IRS) proteins were unaffected by LAR knock-down. These results identify LAR as a crucial regulator of the sensitivity of two key insulin signalling pathways to insulin. Moreover, the siRNA probe provides a molecular tool of general applicability for further dissecting the precise targets and roles of LAR.

摘要

为了测试白细胞共同抗原相关蛋白酪氨酸磷酸酶(LAR)作为胰岛素受体(IR)信号调节因子的作用,开发了一种针对LAR的小干扰RNA(siRNA)探针。LAR的敲低诱导了受体后胰岛素抵抗,胰岛素诱导的蛋白激酶B(PKB)/蛋白激酶Akt(Akt)和丝裂原活化蛋白激酶(MAP激酶)的激活受到显著抑制。IR和胰岛素受体底物(IRS)蛋白的磷酸化和去磷酸化不受LAR敲低的影响。这些结果表明LAR是两条关键胰岛素信号通路对胰岛素敏感性的关键调节因子。此外,该siRNA探针为进一步剖析LAR的精确靶点和作用提供了一种具有广泛适用性的分子工具。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验