二甲双胍和雷帕霉素对p21(WAF1/CIP1)表达的差异调控

International Journal of Chronic Diseases Pub Date : 2014-01-01 Epub Date: 2014-03-25 DOI:10.1155/2014/327640
Zoltan Molnar, Ann B Millward, Wai Tse, Andrew G Demaine
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引用次数: 9

摘要

哺乳动物雷帕霉素靶蛋白(mTOR)通路在糖尿病肾病和其他年龄相关疾病的发生发展中起着重要作用。DN的特征之一是p21(WAF1/CIP1)的表达升高。然而,人们对mTOR信号通路在p21调控中的重要性知之甚少。在这里,我们研究了二甲双胍和雷帕霉素对上皮来源细胞系mtor相关表型的影响。本研究报道二甲双胍抑制高糖诱导的p21表达。高葡萄糖在调节细胞大小、增殖和蛋白质合成方面与二甲双胍相反。这些效应与AMPK激活减少有关,影响下游mTOR信号传导。然而,雷帕霉素对mTOR通路的抑制并未对p21的表达产生负面影响,这表明二甲双胍调节mTOR上游的p21。这些发现为AMPK激活可能调节p21表达的假设提供了支持,这可能对糖尿病肾病和其他年龄相关疾病有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

p21(WAF1/CIP1) Expression is Differentially Regulated by Metformin and Rapamycin.

p21(WAF1/CIP1) Expression is Differentially Regulated by Metformin and Rapamycin.

p21(WAF1/CIP1) Expression is Differentially Regulated by Metformin and Rapamycin.

p21(WAF1/CIP1) Expression is Differentially Regulated by Metformin and Rapamycin.

The mammalian target of rapamycin (mTOR) pathway plays an important role in the development of diabetic nephropathy and other age-related diseases. One of the features of DN is the elevated expression of p21(WAF1/CIP1). However, the importance of the mTOR signalling pathway in p21 regulation is poorly understood. Here we investigated the effect of metformin and rapamycin on mTOR-related phenotypes in cell lines of epithelial origin. This study reports that metformin inhibits high glucose-induced p21 expression. High glucose opposed metformin in regulating cell size, proliferation, and protein synthesis. These effects were associated with reduced AMPK activation, affecting downstream mTOR signalling. However, the inhibition of the mTOR pathway by rapamycin did not have a negative effect on p21 expression, suggesting that metformin regulates p21 upstream of mTOR. These findings provide support for the hypothesis that AMPK activation may regulate p21 expression, which may have implications for diabetic nephropathy and other age-related pathologies.

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