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Herbal compound 861 regulates mRNA expression of collagen synthesis- and degradation-related genes in human hepatic stellate cells

机译:草药化合物861调节人肝星状细胞中胶原合成和降解相关基因的mRNA表达

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摘要

AIM: To identify the role of herbal compound 861 (Cpd 861) in the regulation of mRNA expression of collagen synthesis- and degradation-related genes in human hepatic stellate cells (HSCs).METHODS: mRNA levels of collagen typesIand III, matrix metalloproteinase 1 (MMP-1), matrix metalloproteinase 2 (MMP-2), membrane type-1 matrix metalloproteinase (MT1-MMP), tissue inhibitor of metalloproteinase 1 (TIMP-1), and transforming growth factor β1 (TGF-β1) in cultured-activated HSCs treated with Cpd 861 or interferon-γ (IFN-γ) were determined by real-time PCR.RESULTS: Both Cpd 861 and IFN-γ reduced the mRNA levels of collagen type III, MMP-2 and TGF-β1. Moreover, Cpd 861 significantly enhanced the MMP-1 mRNA levels while down-regulated the TIMP-1 mRNA expression, increasing the ratio of MMP-1 to TIMP-1 to (6.3 + 0.3)- fold compared to the control group.CONCLUSION: The anti-fibrosis function of Cpd 861 may be mediated by both decreased interstitial collagen synthesis by inhibiting the transcription of collagen type III and TGF-β1 and increased degradation of these collagens by up-regulating MMP-1 and down-regulating TIMP-1 mRNA levels.
机译:目的:确定草药化合物861(Cpd 861)在调节人类肝星状细胞(HSC)中胶原合成和降解相关基因的mRNA表达中的作用。方法:I型和III型胶原蛋白,基质金属蛋白酶1的mRNA水平(MMP-1),基质金属蛋白酶2(MMP-2),膜1型基质金属蛋白酶(MT1-MMP),金属蛋白酶1组织抑制剂(TIMP-1)和转化生长因子β1(TGF-β1)结果:Cpd 861和IFN-γ均能降低III型胶原,MMP-2和TGF-β1的mRNA水平。此外,Cpd 861显着提高了MMP-1 mRNA水平,同时下调了TIMP-1 mRNA表达,与对照组相比将MMP-1与TIMP-1的比率提高了(6.3 + 0.3)倍。 Cpd 861的抗纤维化功能可能是通过抑制III型胶原和TGF-β1的转录而减少间质胶原合成,以及通过上调MMP-1和下调TIMP-1 mRNA来增加这些胶原的降解所介导的水平。

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