Baicalein alleviated TGF β1-induced type I collagen production in lung fibroblasts via downregulation of connective tissue growth factor

被引:27
|
作者
Sun, Xionghua [1 ]
Cui, Xinjian [1 ]
Chen, Xihua [1 ]
Jiang, Xiaogang [1 ]
机构
[1] Soochow Univ, Coll Pharmaceut Sci, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Baicalein; Human lung fibroblast; Type I collagen; Quantitative proteomics; CTGF; INDUCED PULMONARY-FIBROSIS; NINTEDANIB; BETA; INHIBITION; DEPOSITION; RATS;
D O I
10.1016/j.biopha.2020.110744
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Although we have reported that baicalein ameliorated bleomycin-induced pulmonary fibrosis in rats and inhibited fibroblast-to-myofibroblast differentiation, the mechanisms of the capability of baicalein to suppress the production of type I collagen in fibroblasts remains unclear. Here, we showed that baicalein suppressed transforming growth factor beta 1 (TGF beta 1)-stimulated the production of type I collagen in lung fibroblast MRC-5 cells. By applying SILAC-based proteomic technology, 158 proteins were identified as baicalein-modulated proteins in TGF beta 1-stimulated the accumulation of type I collagen in MRC-5 cells. Our proteomic and biochemical analysis demonstrated that baicalein decreased the expression levels of connective tissue growth factor (CTGF) in TGF beta 1-stimulated MRC-5 cells. In addition, CTGF overexpression elevated the levels of type I collagen in baicalein-treated fibroblasts. Moreover, our results demonstrated that baicalein-downregulated CTGF expression might be related with the decrease of Smad2 phosphorylation, but not SP1. This work not only linked CTGF to TGF beta 1-stimulated the production of type I collagen in its attribution to the effects of baicalein, but also might provide valuable information for enhancing the knowledge of the pharmacological inhibition of collagen production, which might represent a promising strategy for the treatment of pulmonary fibrosis.
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页数:7
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