Effect of resveratrol on PTEN expression and fibrosis of renal tubular epithelial cells in a high-glucose environment.
10.19540/j.cnki.cjcmm.20210520.401
- Author:
Lan SUN
1
;
Xu-Xian WU
2
;
Yu-Fen PENG
3
Author Information
1. Department of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University Guiyang 550025, China.
2. Tissue Engineering and Stem Cell Experimental Center, Guizhou Medical University Guiyang 550025, China.
3. Department of Radiology, Traditional Chinese Medicine Hospital of Qiandongnan Miao and Dong Autonomous Prefecture Kaili 556000, China.
- Publication Type:Journal Article
- Keywords:
PTEN;
SF1670;
fibrosis;
renal tubular epithelial cell;
resveratrol
- MeSH:
Animals;
Epithelial Cells;
Fibrosis;
Glucose;
PTEN Phosphohydrolase/genetics*;
Rats;
Resveratrol/pharmacology*
- From:
China Journal of Chinese Materia Medica
2021;46(18):4793-4799
- CountryChina
- Language:Chinese
-
Abstract:
This study explored the effects of resveratrol(Res) on the expression of phosphatase and tensin homolog deleted on chromosome ten(PTEN) and the fibrosis of rat renal tubular epithelial cells in a high-glucose environment and the possible mechanism underlying the fibrosis reduction. After the pretreatment of rat renal tubular epithelial cells(NRK-52 E) cultured in a high-glucose condition with Res or PTEN inhibitor SF1670, they were divided into several groups, i.e., normal glucose(NG), normal glucose + SF1670(NS), high glucose(HG), high glucose + SF1670(HS), high glucose + Res at different concentrations(5, 10, 25 μmol·L~(-1)). The expression and distribution of E-cadherin and α-SMA in renal tubular epithelial cells were observed by immunofluorescence cytochemistry. The protein expression levels of PTEN, E-cadherin, α-SMA, p-Akt~((Thr308)) and collagen Ⅳ were determined by Western blot. Real-time PCR was employed to detect the expression of PTEN mRNA. Compared with the NG group, the HG group witnessed the reduced expression of PTEN mRNA, PTEN protein and E-cadherin protein, but saw the increased expression of α-SMA, p-Akt~((Thr308)) and collagen Ⅳ proteins. Besides, with the increase in Res concentration, the expression levels of PTEN mRNA, PTEN protein and E-cadherin protein gradually increased, while those of α-SMA, collagen Ⅳ, p-Akt~((Thr308)) proteins gradually decreased in the Res groups, showing a dose-effect dependence, compared with the HG group. No distinct difference was found between the NS group and the NG group. The expression level of E-cadherin was even lower and those of α-SMA, p-Akt~((Thr308)), and collagen Ⅳ were higher in the HS group than in the HG group, with no marked difference shown in the two groups in terms of PTEN mRNA and protein. Although the PTEN inhibitor did not affect PTEN, the expression changes of the other proteins were opposite to the results after Res treatment and the fibrosis was aggravated, which suggested that SF1670 promoted the fibrosis by inhibiting PTEN, activating Akt and increasing the synthesis of collagen Ⅳ and other extracellular matrix. The results show that Res can antagonize the high glucose-mediated fibrosis of renal tubular epithelial cells. This may be achieved via the up-regulation of PTEN and the inhibition of PI3 K/Akt signaling pathway.
