糖尿病患者肾基质代谢调节的信号机制。

Experimental Diabetes Research Pub Date : 2012-01-01 Epub Date: 2012-02-19 DOI:10.1155/2012/749812
Meenalakshmi M Mariappan
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引用次数: 49

摘要

肾脏肥大和细胞外基质蛋白积聚是糖尿病肾病的主要表现。TGF β系统参与了这些表现的发病机制。在糖尿病肾脏激活的信号通路中,mTOR-(哺乳动物雷帕霉素靶蛋白)调控通路在协调高糖诱导的ECM蛋白产生中起关键作用,导致肾脏功能和结构变化,最终导致不良后果。了解影响个体基质蛋白表达的信号通路可能会导致新的干预策略的发展。本文将重点介绍由高血糖刺激的信号网络的一些不同组成部分,重点介绍糖尿病肾脏的细胞外基质蛋白代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Signaling mechanisms in the regulation of renal matrix metabolism in diabetes.

Signaling mechanisms in the regulation of renal matrix metabolism in diabetes.

Renal hypertrophy and accumulation of extracellular matrix proteins are among cardinal manifestations of diabetic nephropathy. TGF beta system has been implicated in the pathogenesis of these manifestations. Among signaling pathways activated in the kidney in diabetes, mTOR- (mammalian target of rapamycin-)regulated pathways are pivotal in orchestrating high glucose-induced production of ECM proteins leading to functional and structural changes in the kidney culminating in adverse outcomes. Understanding signaling pathways that influence individual matrix protein expression could lead to the development of new interventional strategies. This paper will highlight some of the diverse components of the signaling network stimulated by hyperglycemia with an emphasis on extracellular matrix protein metabolism in the kidney in diabetes.

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来源期刊
Experimental Diabetes Research
Experimental Diabetes Research 医学-内分泌学与代谢
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