间充质干细胞通过恢复肝细胞生长因子和转化生长因子-β1之间的相互平衡,减弱肾小管上皮细胞的上皮间充质转化

Junjun Wei, L. Tang, Shu-wei Zhang, Liangliang Chen, Zhenhua Xie, R. Yu, Hong-Gang Qi, Jiang-yong Lou, Guobin Weng
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摘要

目的:间充质干细胞(MSCs)最近显示出治疗各种类型慢性肾脏疾病模型的希望。然而,这种效应的机制仍然没有得到很好的理解。我们的研究旨在探讨MSCs对转化生长因子-β1 (TGF-β1)诱导的肾小管上皮细胞(HK-2细胞)EMT的影响,以及肝细胞生长因子(HGF)与TGF-β1相互平衡的潜在机制。方法:用TGF-β1处理HK-2细胞,然后与MSCs共培养。通过观察细胞形态、α-平滑肌肌动蛋白(α-SMA)和EMT相关蛋白的表达来评估EMT的诱导效果。采用MTT法和流式细胞术检测TGF-β1和MSCs对HK-2细胞增殖和凋亡的影响。转染抗肝细胞生长因子(siHGF)的SiRNA,降低HGF的表达,以确定HGF在MSCs抑制HK-2 EMT中的作用。结果:TGF-β1降低HK-2细胞HGF表达,诱导EMT,抑制增殖,促进细胞凋亡;但当与间充质干细胞共同培养时,所有结果都相反。然而,在用siHGF治疗后,从MSCs获得的所有益处都消失了。结论:TGF-β1是肾细胞EMT的激活因子,可抑制HGF的表达。然而,MSCs通过提高HGF水平和降低TGF-β1水平对EMT有保护作用。我们的结果也证明了HGF是MSCs抗纤维化的关键因子之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mesenchymal Stem Cells Attenuate the Renal Tubular Epithelial Cells Epithelial Mesenchymal Transition by Restoring the Reciprocal Balance between Hepatocyte Growth Factor and Transforming Growth Factor-β1
Objective: Mesenchymal stem cells (MSCs) have recently shown promise for the treatment of various types of chronic kidney disease models. However, the mechanism of this effect is still not well understood. Our study is aimed to investigate the effect of MSCs on transforming growth factor-β1 (TGF-β1)-induced EMT in renal tubular epithelial cells (HK-2 cells) and the underlying mechanism related to the reciprocal balance between hepatocyte growth factor (HGF) and TGF-β1.Methods: HK-2 cells were treated with TGF-β1-then co-cultured with MSCs. The induced EMT was assessed by cellular morphology and the expressions of alpha-smooth muscle actin (α-SMA) and EMT-related proteins. MTT assay and flow cytometry were employed to detect the effect of TGF-β1 and MSCs on HK-2 cell proliferation and apoptosis. SiRNA against hepatocyte growth factor (siHGF) was transfected to decrease the expression of HGF to identify the role of HGF in MSCs inhibiting HK-2 EMT.Results: TGF-β1 decreased HGF expression, induced EMT, suppressed proliferation and promoted apoptosis in HK-2 cells; but when co-cultured with MSCs all the outcomes were reversed. However, after treated with siHGF, all the benefits taken from MSCs vanished.Conclusion: TGF-β1 was a motivating factor of renal cell EMT and it suppressed the HGF expression. However, MSCs provided protection against EMT by increasing HGF level and decreasing TGF-β1 level. Our results also demonstrated HGF is one of the critical factor in MSCs anti-fibrosis.
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