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CTGF shRNA对肝星状细胞细胞因子及细胞外基质表达的影响

主余华1,李肖红2,张春清1,任万华1,赵幼安3,马艳丽1   

  1. 山东大学 1.山东省立医院消化内科, 山东 济南 250021;2. 西校区校医院, 山东 济南 250012; 3.齐鲁医院消化内科, 山东 济南 250012
  • 收稿日期:2005-11-16 修回日期:1900-01-01 出版日期:2007-06-24 发布日期:2007-06-24
  • 通讯作者: 任万华

Effect of CTGF shRNA on expressions of TGFβ1, CTGF mRNA and extracellular matrix secretion in rat hepatic stellate cells

ZHU Yu-hua1,LI Xiao-hong2,ZHANG Chun-qing1,REN Wan-hua1,ZHAO You-an3,MA Yan-li1   

  1. 1. Department of Gastroenterology, Shandong Provincial Hospital;2. Western Campus Hospital of Shandong University;3. Department of Gastroenterology, Qilu Hospital of Shandong University
  • Received:2005-11-16 Revised:1900-01-01 Online:2007-06-24 Published:2007-06-24
  • Contact: REN Wan-hua

摘要: 目的:研究结缔组织生长因子(CTGF)短发夹RNA(short hairpin RNA,shRNA)对肝星状细胞(HSC-T6)中TGF-β1、CTGF、Ⅰ型胶原、Ⅲ型胶原基因表达及细胞外基质分泌的影响。方法:将已构建并筛选有效含绿色荧光蛋白(EGFP)的CTGFshRNA质粒以转染试剂Metafectene转染HSC-T6,另设空质粒组、只加Metafectene组及空白对照组,24h及48h后,用RT-PCR法检测各组细胞中TGF-β1、CTGF、Ⅰ型胶原、Ⅲ型胶原mRNA的表达;放免法分析细胞上清液中Ⅲ型前胶原、Ⅳ型胶原、透明质酸和层粘连蛋白的含量;流式细胞仪分析转染效率。结果:CTGFshRNA质粒在肝星状细胞的转染效率24h、48h分别为(60±5)%、(42±3)%;与空白对照组相比,空质粒组、脂质体组对基因表达及细胞外基质的分泌均无影响,而CTGFshRNA能明显抑制CTGF、Ⅰ型胶原、Ⅲ型胶原mRNA的表达,降低上清液中Ⅲ型前胶原、Ⅳ型胶原、透明质酸和层粘连蛋白的含量(P<0.01或P<0.05),而对TGF-β1的基因表达则无影响。结论:CTGFshRNA可明显抑制肝星状细胞CTGF、Ⅰ型胶原、Ⅲ型胶原基因表达及细胞外基质的分泌。

关键词: 肝纤维化 , 结缔组织生长因子, 短发夹RNA, 转化生长因子β, RNA干扰

Abstract: Objective:To investigate the effect of CTGF short hairpin RNA(shRNA) on the expression of TGF-β1, CTGF, type Ⅰ procollagen, type Ⅲ procollagen mRNA and extracellular matrix secretion in HSC-T6. Methods: The CTGFshRNA plasmids containing EGFP successfully constructed and screened, were transfected to HSC-T6 with the transfection reagent Metafectene. There were another three HSC-T6 groups: one with plasmids and without CTGFshRNA, one with only Metafectene, and one untreated. The expression of TGF-β1, CTGF, type Ⅰ procollagen and type Ⅲ procollagen mRNA levels were determined by reverse transcriptionpolymerase chain reaction (RTPCR) after 24 and 48 hours. The content of precollagen type Ⅲ, Ⅳtype collagen, and hyaluronate (HA), laminin (LN) in the supernatants were determined by radioimmunoassay. Cell transfection efficiency was analyzed by flow cytometry. Results: The transfection efficiency of CTGFshRNA plasmids in HSC were (60±5)%, (42±3)% at 24 and 48 hours respectively.Compared with those of the blank control, there was no difference in the expression of genes and extracellular matrix secretion in HSC-T6 in the other groups, the group with plasmids and without CTGF shRNA and the group with only Metafectene. Expression of CTGF, type Ⅰ collagen and type Ⅲ collagen mRNA were markedly downregulated in CTGFshRNA transfected HSC-T6(P<0.01 or P<0.05). But there was no difference in the expression of TGF-β1 mRNA. The contents of precollagen type Ⅲ, Ⅳtype collagen, hyaluronate (HA) , and laminin (LN) in the supernatants decreased significantly in CTGFshRNA transfected HSCT6(P<0.01 or P<0.05). Conclusion: CTGFshRNA can regulate the gene expression of the growth factor and the extracellular matrix molecule and inhibits the extracellular matrix secretion in HSCT6.

Key words: RNA interference, Short hairpin RNA, Transforming growth factor β, Connective tissue growth factor, Liver fibrosis

中图分类号: 

  • R503
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