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

被引:10
|
作者
Li, Jun [1 ,2 ]
Dong, Ni [1 ,2 ]
Cheng, Shuang [3 ]
Li, Xiaosheng [3 ]
Wang, Wenli [3 ]
Xiang, Ying [3 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp Stomatol, Dept Endodont, Chongqing 400010, Peoples R China
[2] Chongqing Key Lab Oral Dis & Biomed Sci, Chongqing 401147, Peoples R China
[3] Chongqing Med Univ, Affiliated Hosp 2, Dept Gastroenterol, Chongqing 400010, Peoples R China
关键词
tetramethylpyrazine; TGF-1; connective tissue growth factor; Smad; hepatic stellate cells; TISSUE GROWTH-FACTOR; LIVER FIBROSIS; TGF-BETA; FIBROGENESIS; ACTIVATION;
D O I
10.1080/13102818.2014.984382
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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.
引用
收藏
页码:124 / 131
页数:8
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