[Danshen Injection inhibits peritoneal dialysis fluid-induced endothelial-mesenchymal transition in HMrSV5 cells by regulating the TGF-β/Smad signaling pathway].

Lihua Yu, Jingya Li, Xiaoqi Wang, Li Li, Ya Chen, Feiyu Wang, Kun Zhang, Tongsheng Wang
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Abstract

Objectives: To investigate the inhibitory effect of Danshen Injection on endothelial-mesenchymal transition (EndMT) induced by peritoneal dialysis fluid in HMrSV5 cells and the role of the TGF‑β/Smad signaling pathway in mediating this effect.

Methods: HMrSV5 cells cultured in 40% peritoneal dialysis solution for 72 h to induce EndMT were treated with 0.05%, 0.1% and 0.5% Danshen Injection. CCK-8 assay was used to assess the changes in viability of the treated cells, and the levels of interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), transforming growth factor-β (TGF-β), and vascular endothelial growth factor (VEGF) in the cell supernatant were detected using ELISA; Western blotting was performed to detect the protein expressions of E-cadherin, α-smooth muscle actin (α-SMA), p-Smad 2/3, and Smad 7 in the cells.

Results: Culture in 40% peritoneal dialysis fluid for 72 induced significant EndMT in HMrSV5 cells, which exhibited obviously lowered cell viability. Danshen Injection within the concentration range of 0.025%-1.5% did not significantly affect the viability of the cells. Exposure of HMrSV5 cells to peritoneal dialysis fluid for 72 h significantly increased the production of IL-6, TNF‑α, TGF‑β and VEGF, upregulated the protein expressions of α‑SMA and p-Smad 2/3, and lowered the expressions of E-cadherin and Smad7 proteins. Treatment of the exposed cells with Danshen injection significantly increased cell viability and cellular expressions of E-cadherin and Smad 7 proteins and reduced the production of IL-6, TNF-α, TGF-β and VEGF and the protein expressions of α‑SMA and p-Smad 2/3.

Conclusions: Danshen Injection can suppress peritoneal dialysis fluid-induced EndMT in HMrSV5 cells possibly by regulating the TGF-β/Smad signaling pathway.

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[丹参注射液通过调节TGF-β/Smad信号通路抑制腹膜透析液诱导的HMrSV5细胞内皮-间质转化]。
目的:探讨丹参注射液对腹膜透析液诱导的HMrSV5细胞内皮-间充质转化(EndMT)的抑制作用及TGF - β/Smad信号通路在其中的作用。方法:HMrSV5细胞在40%腹膜透析液中培养72 h诱导EndMT,分别用0.05%、0.1%和0.5%丹参注射液处理。采用CCK-8法检测处理后细胞活力变化,ELISA法检测细胞上清中白细胞介素-6 (IL-6)、肿瘤坏死因子-α (TNF-α)、转化生长因子-β (TGF-β)、血管内皮生长因子(VEGF)水平;Western blotting检测细胞中E-cadherin、α-平滑肌肌动蛋白(α-SMA)、p- smad2 /3、smad7蛋白的表达。结果:在40%腹膜透析液中培养72例HMrSV5细胞可诱导显著的EndMT,细胞活力明显降低。丹参注射液在0.025% ~ 1.5%浓度范围内对细胞活力无明显影响。HMrSV5细胞暴露于腹膜透析液72 h后,IL-6、TNF - α、TGF - β和VEGF的产生显著增加,α - SMA和p-Smad 2/3蛋白表达上调,E-cadherin和Smad7蛋白表达下调。丹参注射液可显著提高暴露细胞的细胞活力和E-cadherin、Smad 7蛋白的表达,降低IL-6、TNF-α、TGF-β、VEGF的产生以及α - SMA、p-Smad 2/3蛋白的表达。结论:丹参注射液可能通过调节TGF-β/Smad信号通路抑制腹膜透析液诱导的HMrSV5细胞的EndMT。
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来源期刊
南方医科大学学报杂志
南方医科大学学报杂志 Medicine-Medicine (all)
CiteScore
1.50
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发文量
208
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