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Tetramethylpyrazine inhibits CTGF and Smad2/3 expression and proliferation of hepatic stellate cells

机译:川methyl嗪抑制肝星状细胞CTGF和Smad2 / 3的表达和增殖

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摘要

To study the effects of tetramethylpyrazine (TMP) on the proliferation of hepatic stellate cells-T6 (HSC-T6), and the expression of connective tissue growth factor (CTGF) and Smad2/3 in these cells, HSC-T6 cells were cultured with TMP at different concentrations after transforming growth factor-1 (TGF-1) stimulation. MTT assay was used to assess the cell proliferation. Cells were divided into the control group, TGF-1-treated group and TMP-treated groups, which were treated with different concentrations of TMP. Immunocytochemistry and western blot were performed to detect the expression levels of CTGF and Smad2/3 in HSC-T6 cells. MTT analysis indicated that TMP significantly inhibited the proliferation of HSC-T6 cells, in dose-dependent and time-dependent manners. Immunocytochemistry detection and western blot showed that TMP could diminish TGF-1-induced CTGF over-expression in HSC-T6 cells. Similarly, the enhancing effects of TGF-1 on Smad2/3 expressions in HSC-T6 cells could also be counteracted by TMP treatment. Nuclear translocation of Smad2/3 was blocked by TMP treatment. Correlation analysis suggested a positive correlation between CTGF and Smad2/3 expression levels in HSC-T6 cells. TMP exerts anti-hepatic fibrosis effect through decreasing the expression of CTGF and Smad2/3, as well as inhibiting the proliferation of HSC-T6 cells. Our study provides cellular and molecular bases for further application of TMP in the clinical treatment for hepatic fibrosis.
机译:为了研究四甲基吡嗪(TMP)对肝星状细胞-T6(HSC-T6)增殖以及结缔组织生长因子(CTGF)和Smad2 / 3在这些细胞中的表达的影响,将HSC-T6细胞与转化生长因子1(TGF-1)刺激后,不同浓度的TMP。使用MTT测定法评估细胞增殖。将细胞分为对照组,TGF-1处理组和TMP处理组,分别用不同浓度的TMP处理。免疫细胞化学和免疫印迹法检测HSC-T6细胞中CTGF和Smad2 / 3的表达水平。 MTT分析表明,TMP以剂量依赖性和时间依赖性方式显着抑制HSC-T6细胞的增殖。免疫细胞化学检测和免疫印迹表明,TMP可以减少TSC-1诱导的HSC-T6细胞中CTGF的过度表达。类似地,TMP处理也可以抵消TGF-1对HSC-T6细胞中Smad2 / 3表达的增强作用。 SMP2 / 3的核易位被TMP处理所阻断。相关分析表明,HSC-T6细胞中CTGF与Smad2 / 3表达水平呈正相关。 TMP通过降低CTGF和Smad2 / 3的表达以及抑制HSC-T6细胞的增殖而发挥抗肝纤维化作用。我们的研究为TMP在肝纤维化的临床治疗中的进一步应用提供了细胞和分子基础。

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