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

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收录情况: ◇ SCIE ◇ 统计源期刊

单位: [1]Beijing Genom Inst, Beijing 101300, Peoples R China [2]Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing 101300, Peoples R China [3]Capital Univ Med Sci, Beijing Friendship Hosp, Liver Res Ctr, Beijing 101300, Peoples R China [4]Chinese Acad Med Sci, Inst Med Plant Dev, Beijing 101300, Peoples R China
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关键词: herbal compound 861 human hepatic stellate cells collagen synthesis and degration collagen type III matrix metalloproteinase 1 tissue inhibitor of metalloproteinase 1

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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 types I and 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 beta 1 (TGF-beta 1) in cultured-activated HSCs treated with Cpd 861 or interferon-gamma (IFN-gamma) were determined by real-time PCR. RESULTS: Both Cpd 861 and IFN-gamma reduced the mRNA levels of collagen type III, MMP-2 and TGF-beta 1. 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 sythesis by inhibiting the transcription of collagen type M and TGF-beta 1 and increased degradation of these collagens by up-regulating MMP-1 and down-regulating TIMP-1 mRNA levels. (c) 2008 WJG. All rights reserved.

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出版当年[2007]版:
最新[2025]版:
大类 | 3 区 医学
小类 | 4 区 胃肠肝病学
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出版当年[2006]版:
最新[2023]版:
Q1 GASTROENTEROLOGY & HEPATOLOGY

影响因子: 最新[2023版] 最新五年平均[2021-2025] 出版当年[2006版] 出版当年五年平均[2002-2006] 出版前一年[2005版]

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第一作者单位: [1]Beijing Genom Inst, Beijing 101300, Peoples R China [2]Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing 101300, Peoples R China
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