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干扰素α对肝纤维化鼠星状细胞I和Ⅲ型前胶原mRNA表达及胶原?…
引用本文:张其胜,王吉耀.干扰素α对肝纤维化鼠星状细胞I和Ⅲ型前胶原mRNA表达及胶原?…[J].中华医学杂志,1999,79(9):695-698.
作者姓名:张其胜  王吉耀
摘    要:目的 观察干扰素α对大鼠纤维化时星状细胞增殖,I,Ⅲ型前胶原mRNA表达和肝脏胶原沉积的影响。方法 以CCl4制造肝纤维化模型,培养肝星状细胞,抽提RNA,用地高辛标记I,Ⅲ型前胶原和胶原酶cDnA探针,Northern杂交分析I,Ⅲ型前胶原和胶原酶mRNA表达,Dotblot测定大鼠肝I,Ⅲ型胶原沉积,分别用^3H-TdR和^3H-脯氨酸掺入观察干扰素α对星状细胞增殖和胶原合成的影响。结果 干扰

关 键 词:干扰素α  肝纤维化  溶胶原  mRNA

Effects of interferon-alpha on the mRNA expression of procollagen type I and III of hepatic stellate cells and on the deposition of collagen type I and III in fibrotic liver of rats]
Q Zhang,J Wang,M Hu.Effects of interferon-alpha on the mRNA expression of procollagen type I and III of hepatic stellate cells and on the deposition of collagen type I and III in fibrotic liver of rats][J].National Medical Journal of China,1999,79(9):695-698.
Authors:Q Zhang  J Wang  M Hu
Institution:Department of Gastroenterology, Zhongshan Hospital of Shanghai Medical University, Shanghai 200032.
Abstract:OBJECTIVE: To observe the effects of interferon-alpha on the proliferation and mRNA expression of procollagen type I and III and on the deposition of collagen type I and III in fibrotic liver of rats. METHODS: CCl4 was used to induce the liver fibrosis rat model. The stellate cells were isolated from liver and cultured in DMEM medium. The effects of interferon-alpha on the proliferation and collagen synthesis of stellate cells were determined with 3H-TdR, 3H-proline incorporating test. Total RNA of stellate cells was extracted and the cDNA of procollagen type I and III and of interstitial collagenase was labeled using Dig High Primer technique. The level of procollagen type I and III and interstitial collagenase mRNA were measured by Northern blot analysis. Deposition of collagen type I and III in fibrotic liver was evaluated with Dot blot. RESULTS: At the 4th, 24th and 48th hour, interferon-alpha inhibited the intake of 3H-TdR and 3H-proline by stellate cells significantly. The inhibition rates were 16%, 19% and 27%, respectively. The intensity of inhibition was proportional to the concentration of interferon-alpha. The expression level of procollagen type I and III mRNA in the interferon-alpha treated group was significantly lower than that in control group in all stages of fibrosis. At the 2nd and 6th week, the deposition of collagen type I and III in interferon-alpha treated group decreased significantly compared with that in control group. However, no difference was found at the 9th week. The expression of collagenase mRNA between interferon-alpha treated group and control group showed no difference. CONCLUSION: Interferon-alpha can inhibid the proliferation and collagen synthesis of stellate cells, down-regulate the expressions of procollagen type I and III mRNA and reduce the deposition of collagen type I and III in fibrotic liver. It has no effect on collagenase.
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