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胰岛素作用和抵抗的组织特异性。

Tissue-specificity of insulin action and resistance.

机构信息

Departamento de Bioquímica y Biología Molecular II, Facultad de Farmacia, Universidad Complutense, Madrid, Spain.

出版信息

Arch Physiol Biochem. 2011 Jul;117(3):96-104. doi: 10.3109/13813455.2011.563748. Epub 2011 Apr 20.

Abstract

Insulin resistance is the most important pathophysiological feature in many pre-diabetic states. Type 2 diabetes mellitus is a complex metabolic disease and its pathogenesis involves abnormalities in both peripheral insulin action and insulin secretion by pancreatic beta cells. The creation of monogenic or polygenic genetically manipulated mice models in a tissue-specific manner was of great help to elucidate the tissue-specificity of insulin action and its contribution to the overall insulin resistance. However, complete understanding of the molecular bases of the insulin action and resistance requires the identification of the intracellular pathways that regulate insulin-stimulated proliferation, differentiation and metabolism. Accordingly, cell lines derived from insulin target tissues such as brown adipose tissue, liver and beta islets lacking insulin receptors or sensitive candidate genes such as IRS-1, IRS-2, IRS-3, IR and PTP1B were developed. Indeed, these cell lines have been also very useful to understand the tissue-specificity of insulin action and inaction.

摘要

胰岛素抵抗是许多糖尿病前期状态中最重要的病理生理特征。2 型糖尿病是一种复杂的代谢性疾病,其发病机制涉及外周胰岛素作用和胰腺β细胞胰岛素分泌的异常。通过组织特异性方式创建单基因或多基因遗传操作的小鼠模型,对于阐明胰岛素作用的组织特异性及其对整体胰岛素抵抗的贡献非常有帮助。然而,要完全了解胰岛素作用和抵抗的分子基础,需要确定调节胰岛素刺激的增殖、分化和代谢的细胞内途径。因此,开发了来自胰岛素靶组织(如棕色脂肪组织、肝脏和β胰岛)的细胞系,这些细胞系缺乏胰岛素受体或敏感的候选基因,如 IRS-1、IRS-2、IRS-3、IR 和 PTP1B。事实上,这些细胞系对于理解胰岛素作用和失效的组织特异性也非常有用。

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