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姜黄素通过TLR4-NF-κB信号通路对高糖诱导的肾小管上皮细胞上皮-间质转化的影响

Effects of Curcumin on High Glucose-Induced Epithelial-to-Mesenchymal Transition in Renal Tubular Epithelial Cells Through the TLR4-NF-κB Signaling Pathway.

作者信息

Liu Xinhui, Zhang Xiuli, Cai Xiaoyi, Dong Jiqiu, Chi Yinmao, Chi Zhihong, Gu Harvest F

机构信息

Traditional Chinese Medicine, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning Province, 110847, People's Republic of China.

Department of Nephrology, Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong Province, 518000, People's Republic of China.

出版信息

Diabetes Metab Syndr Obes. 2021 Mar 2;14:929-940. doi: 10.2147/DMSO.S296990. eCollection 2021.

Abstract

OBJECTIVE

Diabetic kidney disease (DKD) is a microvascular complication in diabetes mellitus, while tubuloepithelial to mesenchymal transition (EMT) of mature tubular epithelial cells is a key point in the early development and progression of renal interstitial fibrosis. The present study aimed to investigate the protective effects of Curcumin on EMT and fibrosis in cultured normal rat kidney tubular epithelial cell line (NRK-52E).

METHODS

By using immunofluorescence staining and Western blot protocols, in vitro experiments were designed to analyze EMT markers, including collagen I and E-cadherin in high glucose (HG) exposed NRK-52E cells and to detect the expression levels of phosphorylated-NF-κB, TLR4 and reactive oxygen species (ROS) after Curcumin pre-treatment. With co-treatment with TAK242, these molecules in the TLR4-NF-κB signaling pathway were further evaluated.

RESULTS

Curcumin decreased the HG-induced EMT levels and ROS production in NRK-52E cells. Furthermore, Curcumin was found to inhibit the TLR4-NF-κB signaling activation in HG-induced EMT of NRK-52E cells.

CONCLUSION

The present study provides evidence suggesting a novel mechanism that Curcumin exerts the anti-fibrosis effects via inhibiting activation of the TLR4-NF-κB signal pathway and consequently protecting the HG-induced EMT in renal tubular epithelial cells. Thereby, TLR4-NF-κB may be a useful target for therapeutic intervention in DKD.

摘要

目的

糖尿病肾病(DKD)是糖尿病的一种微血管并发症,而成熟肾小管上皮细胞的上皮-间质转化(EMT)是肾间质纤维化早期发生和进展的关键环节。本研究旨在探讨姜黄素对培养的正常大鼠肾小管上皮细胞系(NRK-52E)中EMT和纤维化的保护作用。

方法

通过免疫荧光染色和蛋白质印迹法,设计体外实验分析高糖(HG)处理的NRK-52E细胞中的EMT标志物,包括Ⅰ型胶原和E-钙黏蛋白,并检测姜黄素预处理后磷酸化核因子κB(NF-κB)、Toll样受体4(TLR4)和活性氧(ROS)的表达水平。与TAK242共同处理后,进一步评估TLR4-NF-κB信号通路中的这些分子。

结果

姜黄素降低了HG诱导的NRK-52E细胞中的EMT水平和ROS生成。此外,发现姜黄素抑制HG诱导的NRK-52E细胞EMT中的TLR4-NF-κB信号激活。

结论

本研究提供了证据,提示一种新机制,即姜黄素通过抑制TLR4-NF-κB信号通路的激活,从而保护肾小管上皮细胞中HG诱导的EMT,发挥抗纤维化作用。因此,TLR4-NF-κB可能是DKD治疗干预的一个有用靶点。

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