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过氧化物酶增生物激活受体γ激动剂对肝星状细胞α1(I)胶原表达的影响

Effects of PPARγ Agonist on the Expression of Procollagen α1(Ⅰ) in Hepatic Stellate Cells

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【作者】 康谊王天才尚佳杨玉秀李修龄

【Author】 Kang Yi~(1),Wang Tiancai~(2),Shang Jia~(1) et al~(1)Department of Gastroenterological Medicine,People’s Hospital of Henan Province,Zhengzhou 453003~(2)Department of Gastroenterological Medicine,Tongji Hospital,Tongji Medical College, Huazhong University of Science and Technology,Wuhan 430030

【机构】 河南省人民医院消化内科华中科技大学同济医学院附属同济医院消化内科河南省人民医院消化内科 郑州453003武汉430030郑州453003

【摘要】 目的观察过氧化物酶增生物激活受体γ(PPARγ)激动剂15d-PGJ2对肝星状细胞株(HSC-T6)前胶原α1(Ⅰ)表达的影响,以进一步探讨PPARγ在肝纤维化进程中的作用机制。方法体外培养HSC-T6细胞,取对数生长期的细胞分为空白对照组、TGFβ-对照组和15d-PGJ2处理组,TGF-β对照组和15d-PGJ2处理组均给予TGF-β因子(终浓度3 ng/ml)共孵育6 h,15d-PGJ2处理组再用1、2、3μmol/L的PPARγ激动剂15d-PGJ2作用24 h。应用RT-PCR、Westernblot方法观察分析各组间肝星状细胞PPARγ、前胶原α1(Ⅰ)基因表达的变化。结果15d-PGJ2能够显著上调PPARγmRNA和蛋白的表达水平,15d-PGJ2处理组的相对吸光度值较空白对照明显升高(P<0.05),而TGFβ-对照组与空白对照组差异无显著性意义(P>0.05)。在TGFβ-刺激下,TGF-β对照组前胶原α1(Ⅰ)mRNA水平均升高,同空白对照组相比差异有显著性意义(P<0.05);15d-PGJ2处理组细胞前胶原α1(Ⅰ)mRNA水平与空白对照组相比差异无显著性意义(P>0.05),但与TGFβ-对照组相比,其表达明显受抑制(P<0.05)。结论PPARγ激动剂15d-PGJ2能够通过上调PPARγ表达而抑制前胶原α1(Ⅰ)转录,提示PPARγ可抑制肝纤维化的发生发展。

【Abstract】 Objective To investigate the effects of peroxisome proliferator activated receptor γ(PPARγ) agonist 15d-PGJ2 on collagen synthesis in hepatic stellate cells(HSCs),so as to provide experimental evidence for regulating collagen metabolism of HSCs.Methods Rat HSC-T6 cells were cultured in vitro,and were divided into blank control group,TGF-β(final concentration 3 ng/ml) control group and the groups treated with different concentrations of 15d-PGJ2(1,2,3 μmo/L).The expression of procollagen α1(Ⅰ) gene and PPARγ was detected by RT-PCR and Western blot.Results 15d-PGJ2 could significantly up-regulate the expression of PPARγ mRNA and protein.Compared with blank control group,the values of relative absorbance in the groups treated with 15d-PGJ2were obviously increased(P<0.05),whereas there was no difference between blank control group and TGF-β control group(P>0.05).After stimulated with TGF-β,the procollagen α1(Ⅰ) mRNA in TGF-β control group and the groups treated with 15d-PGJ2 were all up-regulated,but there was significant difference in the expression of the procollagen α1(Ⅰ) mRNA between TGF-β control group and the groups treated with 15d-PGJ2.The procollagen α1(Ⅰ) mRNA in the groups treated with 15d-PGJ2 was significantly inhibited as compared with TGF-β control group(P<0.05),but there was no significant difference between blank control group and the groups treated with 15d-PGJ2(P>0.05).Conclusion 15d-PGJ2 could inhibit the transcription of procollagen α1(Ⅰ) gene by up-regulating the expression of PPARγ in HSC-T6,suggesting PPARγ could inhibit the development of liver fibrosis.

  • 【文献出处】 华中科技大学学报(医学版) ,Acta Medicinae Universitatis Scientiae et Technologiae Huazhong , 编辑部邮箱 ,2006年05期
  • 【分类号】R575.2
  • 【被引频次】1
  • 【下载频次】76
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