期刊文献+

PI3K/AKT信号通路在维持血糖平衡中的作用 被引量:25

The functions of PI3K/AKT signaling pathway in glucose homeostasis
原文传递
导出
摘要 近年来,2型糖尿病在全球范围发病率迅速增加,并且有发病时间年轻化的趋势。因此,寻求新的预防和治疗方法成为了亟待解决的问题。胰岛素在维持血糖平衡的过程中起到了不可或缺的作用。胰岛素主要是通过PI3K/AKT信号通路行使其调控血糖的功能。对胰岛素刺激下的PI3K/AKT信号通路的分子机制进行了详细的阐述,分析了在小鼠模型中基因敲除PI3K/AKT信号通路中各个分子以及其负调控因子对糖代谢过程产生的影响,讨论了如何将这些理论研究向临床应用进行转化。另外,还对PAQR3在胰岛素信号通路中的生理功能进行了分析讨论,揭示了一个全新的空间调控胰岛素信号通路的机制。 Type 2 diabetes is a chronic metabolic disease, which is prevalent in nearly all populations in the world and the onset of diabetes is earlier than before. Thus, new therapeutic approaches to counter the increasing threat of type 2 diabetes are in high demand. Insulin is an indispensable regulator of glucose homeostasis. The PI3K/AKT signaling pathway is required for insulin-dependent regulation on cellular metabolism. Here we review the mechanisms of signal transduction implicated in PI3K/AKT and their roles in modulating glucose homeostasis including the studies using transgenic and knockout mouse models. We also discuss how to translate the knowledge of basic research into clinical practice. In addition, we discuss our recent discovery about the regulation of insulin signaling and function by PAQR3.
出处 《生命科学》 CSCD 2013年第2期133-139,共7页 Chinese Bulletin of Life Sciences
基金 国家自然科学基金项目(81021002和81130077)
关键词 2型糖尿病 胰岛素信号通路 PI3K AKT PAQR3 小鼠模型 type 2 diabetes insulin signaling pathway PI3K AKT PAQR3 mouse models
  • 相关文献

参考文献1

二级参考文献49

  • 1Martin BC, Warram JH, Krolewski AS, et al. Role of glucose and insulin resistance in development of type 2 diabetes mellitus: results of a 25-year follow-up study. Lancet 1992; 340:925-929.
  • 2Kahn CR. Banting Lecture. Insulin action, diabetogenes, and the cause of type II diabetes. Diabetes 1994; 43:1066-1084.
  • 3Baudry A, Leroux L, Jackerott M, JoshijRL. Genetic manipulation of insulin signaling, action and secretion in mice. Insights into glucose homeostasis and pathogenesis of type 2 diabetes. EMBO Rep 2002; 3:323-328.
  • 4Li J, Yen C, Liaw D, et al. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science 1997; 275:1943-1947.
  • 5Steck PA, Pershouse MA, Jasser SA, et al. Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat Genet 1997; 15:356-362.
  • 6Butler M, McKay RA, Popoff I J, et al. Specific inhibition of PTEN expression reverses hyperglycemia in diabetic mice. Diabetes 2002; 51:1028-1034.
  • 7Maehama T, Dixon JE. The tumor suppressor, PTEN/MMAC 1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate. JBiol Chem 1998; 273:13375- 13378.
  • 8Stambolic V, Suzuki A, de la Pompa JL, et al. Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN. Cell 1998; 95:29-39.
  • 9Saltiel AR, Kahn CR. Insulin signalling and the regulation of glucose and lipid metabolism. Nature 2001; 414:799-806.
  • 10Stocker H, Andjelkovic M, Oldham S, et al. Living with lethal PIP3 levels: viability of flies lacking PTEN restored by a PH domain mutation in Akt/PKB. Science 2002; 295:2088-2091.

共引文献4

同被引文献246

引证文献25

二级引证文献161

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部