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机构地区:[1]蚌埠医学院免疫学教研室,安徽省感染与免疫重点实验室,安徽蚌埠233030
出 处:《蚌埠医学院学报》2008年第6期652-655,共4页Journal of Bengbu Medical College
基 金:安徽省自然科学基金资助项目(050430603)
摘 要:目的:探讨转录因子维A酸相关孤独受体γt(RORγt)对T细胞亚群产生IFN-γ的调控作用。方法:健康成人外周血单个核细胞用CD3单克隆抗体和IL-2激活和扩增T细胞,活化T细胞用脂质体法转染人工合成的RORγt基因特异性短干扰RNA(siRNA)序列3个片段(RORγt-siRNA-982,-1026,-1197),RT-PCR半定量法检测活化T细胞转染siRNA后RORγt基因表达,流式细胞仪检测不同T细胞亚群产生IFN-γ细胞的比例。结果:活化T细胞转染RORγt-siRNA后,对RORγt基因表达的检测显示,RORγt-siRNA-982序列无抑制作用,而RORγt-siRNA-1026和-1197序列均有明显抑制作用。活化T细胞转染RORγt-siRNA-1026后,产生IFN-γ细胞百分数在CD4+T细胞(32.78±3.41)中,明显低于未转染组(44.54±1.75)(P<0.01)。结论:转录因子RORγt对T细胞,特别是对CD4+T细胞产生IFN-γ有正调控作用。Objective:To investigate the regulation of transcription factor RORγt on the IFN-γ production in different T cell subpopulations.Methods:Peripheral blood mononuclear cells were isolated from peripheral blood of healthy donors by density gradient centrifugation,and were stimulated with CD3 monoclonal antibody and cultured in IL-2 containing medium for 12 days.The activated T cells were transfected with chemical synthesized small interfering RNA(siRNA)sequences for RORγt gene using liposomes.The expression of RORγt gene was detected in RORγt-siRNA transfected T cells by RT-PCR assay.The percentages of IFN-γ producing cells in total T cells,CD4^+ and CD8^+ T cells were measured in the transfected T cells by flowcytometry.Results:By using semi-quantity RT-PCR assay,the RORγt gene expression was inhibited in activated T cells that transfected with RORγt-siRNA-1026 and-1197,but not inhibited in that with RORγt-siRNA-982.Among the RORγt-siRNA-1026 transfected activated T cells,the percentage of IFN-γ producing cells in CD4^+ T cells(32.78±3.41)significantly decreased,compared to untransfected group(44.54±1.75)(P〈0.01).Conclusions:Transcription factor RORγt is involved in the positive regulation for IFN-γ production in CD4^+ T cells.
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