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机构地区:[1]青岛大学医学院免疫学教研室,山东青岛266071
出 处:《细胞与分子免疫学杂志》2011年第2期128-130,134,共4页Chinese Journal of Cellular and Molecular Immunology
基 金:国家自然科学基金资助项目(3170893)
摘 要:目的:研究糖基磷脂酰肌醇(GPI)锚定蛋白CD59对CD55介导T细胞信号转导的增强效应。方法:实验分为未转染的Jurkat细胞组(Ⅰ组)、转染空质粒的Jurkat细胞组(Ⅱ组)及转染CD59干扰质粒的Jurkat细胞组(Ⅲ组)。用RT-PCR检测3组细胞中的CD59基因表达水平。用噻唑蓝(MTT)比色法、免疫印迹技术和激光共聚焦扫描显微镜分别检测CD55与CD59联合作用对3组Jurkat细胞的增殖效应,Src家族酪氨酸激酶(SrcPTK)磷酸化的水平及细胞内钙离子的变化。结果:稳定转染后,Ⅲ组细胞CD59分子的表达被成功抑制。Ⅰ组和Ⅱ组细胞CD55与CD59联合作用后增殖能力,SrcPTK磷酸化水平及钙离子浓度均明显高于Ⅲ组(P<0.05);但Ⅰ组和Ⅱ组之间无差异。结论:CD59可增强CD55对T细胞信号转导的效应。aim:To study the enhancement effect of glycosylphosphatidyl inositol (GPI)-anchored protein CD59 on CD55-mediated T ceil signal transduction. METHODS: Human Jurkat cells were divided into 3 groups: Jurkat cells ( Ⅰgroup), Jurkat cells transfected with blank plasmid ( Ⅱ group) and Jurkat cells transfected with siRNA plasmid ( Ⅲ group). CD59 mRNA level was detected by RT-PCR. The cell proliferation activity of the three groups was measured by MTTcolorimetry after crosslinking anti-CD55 mAb and anti-CD59 mAb. The phosphorylation levels of Src family of protein tyrosine kinase (PTK) were investigated by immunoblot analysis, and the kinetic changes of [ Ca^2+] in T cell endochylema were determined by Laser scanning confocal microscope imaging. RESULTS: CD59 expression was successfullyinhibited in Ⅲgroup cells after transfecting. The cell proliferation, phosphorylation levels of Src family of PTK and degree of [ Ca^2+] in Ⅰ and Ⅱ groups were increased compared with Ill group ( P 〈 0.05 ), after crosslinking of CD55 and CD59 antibodies, but there was no difference between Ⅰ group and Ⅱ group. CONCLUSION: CD59 can enhance the effect of CD55-mediated T cell signal transduction.
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