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转化生长因子-β1/整合素连接激酶/波形蛋白1信号通路在环孢素A诱导培养的肾小管上皮细胞上皮-间质转化中的作用

[Role of TGF-β1/ILK/FSP1 signaling pathway in cyclosporin A-induced epithelialmesenchymal transition in cultured renal tubular epithelial cells].

作者信息

Bai Zhixun, Lu Jing, Yang Yibin

机构信息

Department of Nephrology and Rheumatology, Second Affiliated Hospital of Zunyi Medical University, Zunyi 563000, China.

Zunyi Medical and Pharmaceutical College, Zunyi 563006, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2019 Jul 30;39(7):804-809. doi: 10.12122/j.issn.1673-4254.2019.07.09.

DOI:10.12122/j.issn.1673-4254.2019.07.09
PMID:31340913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6765554/
Abstract

OBJECTIVE

To explore the role of transforming growth factor-β1/integrin-linked kinase/fibroblast-specific protein 1 (TGF- β1/ILK/FSP1) signaling pathway in cyclosporine A (CsA)-induced renal tubular epithelial cell transdifferentiation.

METHODS

Rat renal tubular epithelial NRK-52E cells were induced with 1 mg/L CsA, treated with TGF-β1 inhibitor (SB431542, 10 μmol/L), or transfected with the ILK-RNAi lentiviral expression vector (ILKshRNA) or a negative control vector before CsA induction. The expressions of TGF-β1, ILK and FSP-1 mRNAs and proteins in the cells were detected using real-time PCR and Western blotting. The positive cells for α-SMA expression were detected by immunohistochemistry.

RESULTS

Compared with the blank control cells, the cells treated with CsA showed significantly increased levels of TGF-β1, ILK and FSP-1 mRNAs and proteins ( < 0.05). The expressions of TGF-β1, ILK and FSP-1 were significantly lower in TGF-β1 inhibitor group than in CsA group ( < 0.05). The levels of ILK and FSP-1 were significantly decreased after shRNA-mediated ILK silencing ( < 0.05). The number of positive cells for -SMA was significantly lower in cells treated with SB431542 and in cells with ILK silencing than in the cells treated with CsA alone ( < 0.05).

CONCLUSIONS

The activation of TGF-β1/ILK/FSP-1 signaling pathway is an important mechanism for CsA-induced transdifferentiation in rat renal tubular epithelial cells. ILK participates in CsA-induced epithelialmesenchymal transition of renal tubular epithelial cells.

摘要

目的

探讨转化生长因子-β1/整合素连接激酶/成纤维细胞特异性蛋白1(TGF-β1/ILK/FSP1)信号通路在环孢素A(CsA)诱导肾小管上皮细胞转分化中的作用。

方法

用1mg/L CsA诱导大鼠肾小管上皮NRK-52E细胞,在CsA诱导前用TGF-β1抑制剂(SB431542,10μmol/L)处理,或转染ILK-RNAi慢病毒表达载体(ILKshRNA)或阴性对照载体。采用实时PCR和蛋白质印迹法检测细胞中TGF-β1、ILK和FSP-1 mRNA及蛋白的表达。通过免疫组织化学检测α-SMA表达阳性细胞。

结果

与空白对照细胞相比,CsA处理的细胞中TGF-β1、ILK和FSP-1 mRNA及蛋白水平显著升高(<0.05)。TGF-β1抑制剂组中TGF-β1、ILK和FSP-1的表达明显低于CsA组(<0.05)。shRNA介导的ILK沉默后,ILK和FSP-1水平显著降低(<0.05)。用SB431542处理的细胞和ILK沉默的细胞中α-SMA阳性细胞数明显低于单独用CsA处理的细胞(<0.05)。

结论

TGF-β1/ILK/FSP-1信号通路的激活是CsA诱导大鼠肾小管上皮细胞转分化的重要机制。ILK参与CsA诱导的肾小管上皮细胞上皮-间质转化。

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FSP1-specific SMAD2 knockout in renal tubular, endothelial, and interstitial cells reduces fibrosis and epithelial-to-mesenchymal transition in murine STZ-induced diabetic nephropathy.FSP1 特异性 SMAD2 敲除在肾小管、内皮和间质细胞中可减少 STZ 诱导的糖尿病肾病小鼠的纤维化和上皮间质转化。
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