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黄芩素通过下调结缔组织生长因子减轻 TGF-β1 诱导的肺成纤维细胞 I 型胶原产生。

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

机构信息

College of Pharmaceutical Sciences, Soochow University, China.

College of Pharmaceutical Sciences, Soochow University, China.

出版信息

Biomed Pharmacother. 2020 Nov;131:110744. doi: 10.1016/j.biopha.2020.110744. Epub 2020 Sep 12.

Abstract

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 β1 (TGF β1)-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 β1-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 β1-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 β1-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.

摘要

虽然我们已经报道了黄芩素可以改善博来霉素诱导的大鼠肺纤维化,并抑制成纤维细胞向肌成纤维细胞分化,但黄芩素抑制成纤维细胞产生 I 型胶原的能力的机制尚不清楚。在这里,我们表明黄芩素抑制转化生长因子β1(TGFβ1)刺激的肺成纤维细胞 MRC-5 细胞 I 型胶原的产生。通过应用 SILAC 基于蛋白质组学技术,在 TGFβ1刺激的 MRC-5 细胞中积累 I 型胶原的黄芩素调节蛋白中鉴定出 158 种蛋白。我们的蛋白质组学和生化分析表明,黄芩素降低了 TGFβ1 刺激的 MRC-5 细胞中结缔组织生长因子(CTGF)的表达水平。此外,CTGF 的过表达增加了黄芩素处理的成纤维细胞中 I 型胶原的水平。此外,我们的结果表明,黄芩素下调 CTGF 的表达可能与 Smad2 磷酸化的减少有关,但与 SP1 无关。这项工作不仅将 CTGF 与 TGFβ1 刺激的 I 型胶原产生联系起来,归因于黄芩素的作用,而且可能为增强对胶原产生的药理学抑制的知识提供有价值的信息,这可能代表治疗肺纤维化的有前途的策略。

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