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脂多糖刺激树突状细胞前后TLR2、3、4基因表达的检测
引用本文:董薇,张兵,蔡美英,魏大鹏.脂多糖刺激树突状细胞前后TLR2、3、4基因表达的检测[J].航天医学与医学工程,2005,18(3):216-218.
作者姓名:董薇  张兵  蔡美英  魏大鹏
作者单位:四川大学华西基础医学与法医学院免疫学教研室,四川成都,610041
基金项目:高等学校博士学科点专项科研基金资助(0040105102006)
摘    要:目的 检测脂多糖作用于树突状细胞前后TLR2、3、4基因的表达情况。方法 从外周血分离单核细胞,加入rhGM-CSF及rhIL-4,培养的第6天,实验组加入脂多糖刺激24h,对照组不加。分别提取细胞总RNA,行半定量RT-PCR,产物进行琼脂糖凝胶电泳分析。结果 单核细胞经GM-CSF及IL-4诱导7d后的DC表达较高水平TLR2、3、4。脂多糖刺激24h后,TLR2、3、4表达下降,TLR4几乎测不到。结论 树突状细胞在受脂多糖刺激前后TLRs的表达有显著变化,推测和它的功能成熟有关。

关 键 词:基因表达  脂多糖  树突状细胞  TLRs  半定量RT-PCR
文章编号:1002-0837(2005)03-0216-03

Detection of Gene Expression for TLR2,3,4 on Dendritic Cells before and after Stimulation by Lipopolysaccharide
DONG Wei,ZHANG Bing,CAI Mei-ying,Wei Da-peng.Detection of Gene Expression for TLR2,3,4 on Dendritic Cells before and after Stimulation by Lipopolysaccharide[J].Space Medicine & Medical Engineering,2005,18(3):216-218.
Authors:DONG Wei  ZHANG Bing  CAI Mei-ying  Wei Da-peng
Institution:DONG Wei,ZHANG Bing,CAI Mei-ying,WEI Da-peng.Address reprint requests to:CAI Mei-ying.Department of Immunology,School of West China Basic Medicine and Forensic,Sichuan University,Chengdu Sichuan 610041,China
Abstract:Objective To detect the gene expression for TLR2,3,4 on dendritic cells before and after stimulation by lipopolysaccharide. Method Monocytes were isolated from heparinized whole blood. 7 d later the monocytes were induced into dendritic cells by adding rhGM-CSF and rhIL-4. Total cellular RNA of unstimulated and stimulated DC were extracted by LPS 24 h later. Semi-quantitative RT-PCR,agarose gel electrophoresis were conducted to analyse the PCR products. Result Expression of TLR2,3,4 were significantly higher in monocytes-derived DC induced to 7 d.After being stimulated by LPS for 24 h ,the expression of TLR2,3,4 decreased, and that of TLR4 was almost undetectable. Conclusion The expression of TLR2,3,4 on DC changes significantly after being stimulated by LPS.This may be related to functional maturation of DC.
Keywords:gene expression  lipopolysaccharide  dendritic cells  TLRs  semi-quantitative RT-PCR
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