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作 者:史伟[1] 梁馨苓[1] 刘双信[1] 梁永正[1] 郝文科[1] 杨周灼[1] 余细勇[2]
机构地区:[1]广东省人民医院肾内科,广州510080 [2]心脏病研究所药理研究室
出 处:《中华肾脏病杂志》2002年第2期103-106,共4页Chinese Journal of Nephrology
基 金:广东省科学委员会科技攻关重点项目(199710);广东省医药科学技术研究基金(1997045)
摘 要:目的 观察转化生长因子beta1(TGF-β1)反义RNA对系膜细胞基质合成的影响。方法 构建含TGF-β1反义RNA的重组腺病毒,将重组腺病毒转染系膜细胞,用Northern blot检测转染系膜细胞TGF-β1及ColⅣmRNA的含量,用免疫组化半定量分析转染的系膜细胞中TGF-β1、纤连蛋白(FN)及胶原(Col)Ⅳ蛋白水平,并与无转染的系膜细胞对照组比较其表达的变化。结果 构建了含TGF-β1反义RNA的重组腺病毒。重组反义TGF-β1腺病毒转染系膜细胞后,与对照组相比,在第24hTGF-β1及ColⅣ的mRNA无明显抑制,在48h TGF-β1及ColⅣmRNA抑制率分别为22.5%,18.2%;72h TGF-β1及ColⅣmRNA抑制率分别为29.5%,27.3%。免疫组织化学半定量结果显示:与对照组相比,在48h始转染系膜细胞TGF-β1、FN及ColⅣ蛋白含量开始下降,48hTGF-β1、FN及ColⅣ蛋白抑制率分别为16.5%,18.2%及14.6%;72hTGF-β1、FN及ColⅣ蛋白抑制率分别为23.5%,27.3%及26.8%。结论 重组反义TGF-β1可抑制系膜细胞合成细胞外基质,在肾小球肾炎及肾小球硬化的研究及治疗中有潜在的应用价值。Objective To study the effect of transforming growth factor beta 1(TGF-B1) antisense RNA on synthesis and secretion of extracellular matrix in mesangial cell. Methods The recombinant anlisense TGF-Bl RNA adenovirus was generated. The cultured mesangial cells were transfected by recombinant adenovirus as therapy group, and the mesangial cells were not transfected as control group. The mRNA of TGF-B1 and a1(IV) collagen was analysed by Northern blot, and immunohistochemislry straining was employed for the protein of TGF-Bl, fibronectin and a1 (IV)collagen in both groups of mesangial cells. Results Recombinant antisense TGF-Bl adenovirus was constructed. The mRNA of TGF-B1 and a1(IV) collagen in mesangial cells was repressed by recombinant antisense TGF-Bl adenovirus at 48 hours after transfection in comparison with the control group. The repressed ratio of mRNA in TGF-Bl and a1(IV) collagen was 22. 5% , 18. 2% respectively in mesangial cells at 48 hours after transfection, and 29. 5% , 27. 3% respectively at 72 hours after transfection in comparison with the control group. The protein of TGF-B1, fibronectin and a1(IV) collagen was inhibited, and repressed ratio was 16.5%, 18. 2% and 14. 6% respectively at 48 hours after transfection, and was 23. 5% , 27. 3% and 26. 8% respectively at 72 hours after transfection in comparison with the control group. Conclusion Recombinant antisense TGF-B1 adenovirus inhibits synthesis and secretion of extracellular matrix in mesangial cells which may be effective in gene therapy for proliferative glomerulonephritis and sclerosing glomerulonephritis.
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