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雷帕霉素可预防百草枯诱导的肺纤维化:Nrf2信号通路的激活

Rapamycin protects against paraquat-induced pulmonary fibrosis: Activation of Nrf2 signaling pathway.

作者信息

Xu Yiheng, Tai Wenlin, Qu Xiaoyuan, Wu Wenjuan, Li ZhenKun, Deng Shuhao, Vongphouttha Chanthasone, Dong Zhaoxing

机构信息

Department of Clinical Laboratory, Yunnan Molecular Diagnostic Center, The 2nd Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.

Department of Respiratory, The 2nd Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.

出版信息

Biochem Biophys Res Commun. 2017 Aug 19;490(2):535-540. doi: 10.1016/j.bbrc.2017.06.074. Epub 2017 Jun 15.

Abstract

Paraquat (PQ) is a widely used herbicide indeveloping countries worldwide, and pulmonary fibrosis is one of the most typical features of PQ poisoning. The molecular mechanism of PQ toxicity especially how to treat PQ-induced pulmonary fibrosis is still largely unknown. In animal model of pulmonary fibrosis, we used HE staining, western blotting assay and Real-time PCR assay to analyze the effects of rapamycin on the PQ-induced epithelial mesenchymal transition (EMT). We found that PQ induced the pulmonary fibrosis using HE staining and Masson's staining, and up-regulated the activity of HYP and the mRNA expressions of Collagen I and III (COL-1and COL-3) in pulmonary tissues. We also found that rapamycin down-regulated the mesenchymal cell marker Vimentin and up-regulated the epithelial cell marker E-cadherin both in mRNA and protein levels compared with PQ group. And the EMT associated transcription factor Snail was decreased by rapamycin treatment compared with PQ group. And PQ decreased the Nrf2 expression both in mRNA and protein levels, and rapamycin inhibited these effects of PQ. SFN, a activator of Nrf2, could inhibit the EMT and the expression of Snail. And knockdowon of Nrf2 could abolish the inhibitory effects of rapamycin of PQ-induced EMT. In conclusion, rapamycin protects against paraquat-induced pulmonary fibrosis by activation of Nrf2 signaling pathway.

摘要

百草枯(PQ)是一种在全球发展中国家广泛使用的除草剂,肺纤维化是PQ中毒最典型的特征之一。PQ毒性的分子机制,尤其是如何治疗PQ诱导的肺纤维化,目前仍 largely未知。在肺纤维化动物模型中,我们使用苏木精-伊红(HE)染色、蛋白质印迹分析和实时聚合酶链反应(Real-time PCR)分析来研究雷帕霉素对PQ诱导的上皮-间质转化(EMT)的影响。我们发现,通过HE染色和Masson染色可观察到PQ诱导了肺纤维化,并上调了肺组织中羟脯氨酸(HYP)的活性以及I型和III型胶原蛋白(COL-1和COL-3)的mRNA表达。我们还发现,与PQ组相比,雷帕霉素在mRNA和蛋白质水平上均下调了间充质细胞标志物波形蛋白(Vimentin),并上调了上皮细胞标志物E-钙黏蛋白(E-cadherin)。与PQ组相比,雷帕霉素处理可降低EMT相关转录因子Snail的表达。并且PQ在mRNA和蛋白质水平上均降低了核因子E2相关因子2(Nrf2)的表达,而雷帕霉素抑制了PQ的这些作用。萝卜硫素(SFN)作为Nrf2的激活剂,可抑制EMT和Snail的表达。敲低Nrf2可消除雷帕霉素对PQ诱导的EMT的抑制作用。总之,雷帕霉素通过激活Nrf2信号通路来预防百草枯诱导的肺纤维化。

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