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α-硫辛酸通过mTOR/p70S6K/4E-BP1信号通路调节高糖诱导的大鼠系膜细胞功能障碍

Alpha Lipoic Acid Modulated High Glucose-Induced Rat Mesangial Cell Dysfunction via mTOR/p70S6K/4E-BP1 Pathway.

作者信息

Lv Chuan, Wu Can, Zhou Yue-Hong, Shao Ying, Wang Guan, Wang Qiu-Yue

机构信息

Division of Endocrinology, First Affiliated Hospital, China Medical University, Shenyang, Liaoning 110001, China.

Division of Endocrinology, Shenyang No. 8 Hospital, Shenyang, Liaoning 110024, China.

出版信息

Int J Endocrinol. 2014;2014:658589. doi: 10.1155/2014/658589. Epub 2014 Oct 30.

DOI:10.1155/2014/658589
PMID:25530759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4229972/
Abstract

The aim of this study was to investigate whether alpha lipoic acid (LA) regulates high glucose-induced mesangial cell proliferation and extracellular matrix production via mTOR/p70S6K/4E-BP1 signaling. The effect of LA on high glucose-induced cell proliferation, fibronectin (FN), and collagen type I (collagen-I) expression and its mechanisms were examined in cultured rat mesangial cells by methylthiazol tetrazolium (MTT) assay, flow cytometry, ELISA assay, and western blot, respectively. LA at a relatively low concentration (0.25 mmol/L) acted as a growth factor in rat mesangial cells, promoted entry of cell cycle into S phase, extracellular matrix formation, and phosphorylated AKT, mTOR, p70S6K, and 4E-BP1. These effects disappeared when AKT expression was downregulated with PI3K/AKT inhibitor LY294002. Conversely, LA at a higher concentration (1.0 mmol/L) inhibited high glucose-induced rat mesangial cell proliferation, entry of cell cycle into S phase, and extracellular matrix exertion, as well as phosphorylation of mTOR, p70S6K, and 4E-BP1 but enhanced the activity of AMPK. However, these effects disappeared when AMPK activity was inhibited with CaMKK inhibitor STO-609. These results suggest that LA dose-dependently regulates mesangial cell proliferation and matrix protein secretion by mTOR/p70S6K/4E-BP1 signaling pathway under high glucose conditions.

摘要

本研究旨在探讨α硫辛酸(LA)是否通过mTOR/p70S6K/4E-BP1信号通路调节高糖诱导的系膜细胞增殖和细胞外基质产生。分别采用甲基噻唑四氮唑(MTT)法、流式细胞术、酶联免疫吸附测定(ELISA)法和蛋白质印迹法,检测LA对培养的大鼠系膜细胞中高糖诱导的细胞增殖、纤连蛋白(FN)和I型胶原(collagen-I)表达的影响及其机制。相对低浓度(0.25 mmol/L)的LA在大鼠系膜细胞中起生长因子的作用,促进细胞周期进入S期、细胞外基质形成以及AKT、mTOR、p70S6K和4E-BP1的磷酸化。当用PI3K/AKT抑制剂LY294002下调AKT表达时,这些作用消失。相反,较高浓度(1.0 mmol/L)的LA抑制高糖诱导的大鼠系膜细胞增殖、细胞周期进入S期和细胞外基质分泌,以及mTOR、p70S6K和4E-BP1的磷酸化,但增强了AMPK的活性。然而,当用CaMKK抑制剂STO-609抑制AMPK活性时,这些作用消失。这些结果表明,在高糖条件下,LA通过mTOR/p70S6K/4E-BP1信号通路剂量依赖性地调节系膜细胞增殖和基质蛋白分泌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/83d910ffa6c4/IJE2014-658589.009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/3bf8cd832f98/IJE2014-658589.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/3887424527af/IJE2014-658589.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/f41c0df59031/IJE2014-658589.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/c2b4de0f95cd/IJE2014-658589.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/bc991b17ebf1/IJE2014-658589.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/a396171ffab4/IJE2014-658589.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/08f27c3e0fd6/IJE2014-658589.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/3a48622582aa/IJE2014-658589.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/83d910ffa6c4/IJE2014-658589.009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/3bf8cd832f98/IJE2014-658589.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/3887424527af/IJE2014-658589.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/f41c0df59031/IJE2014-658589.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/c2b4de0f95cd/IJE2014-658589.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/bc991b17ebf1/IJE2014-658589.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/a396171ffab4/IJE2014-658589.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/08f27c3e0fd6/IJE2014-658589.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/3a48622582aa/IJE2014-658589.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1919/4229972/83d910ffa6c4/IJE2014-658589.009.jpg

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