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机构地区:[1]北京医科大学
出 处:《细胞与分子免疫学杂志》1998年第1期8-10,共3页Chinese Journal of Cellular and Molecular Immunology
摘 要:本实验研究了人重组GMCSF对U937人单核细胞样细胞系HLA和CD86分子表达的调节作用。将U937细胞在rGMCSF10μg/L培养1d,HLADR分子的表达率为83%,对照组为91%;培养2d,表达率为51%,对照组为78%;培养5d,表达率为53%,对照组为81%。U937细胞在rGMCSF10μg/L浓度下培养1d,CD86分子表达率为2%,对照组为1.6%;培养3d,表达率为3.91%,对照组为1%;培养5d,表达率为532%,对照组为0.58%。而MHCⅠ类分子表达率在10μg/L浓度下培养5d时,实验组和对照组均为100%。以上结果显示,rGMCSF对U937细胞具有下调MHCⅡ类分子表达和上调CD86分子表达的作用。MHCⅡ类分子和CD86分子是T细胞重要的活化信号分子,因此可以说明,rGMCSF对T细胞参与的免疫应答具有重要的调节意义。We analyzed the effects of human recombinant GM CSF on MHC and CD86 molecule expression on U937 human monocyte like cell line. U937 cells were cultured for one day. The percentages of DR molecule expression were 83% in presence of rGM CSF( 10 μg/L) and medium control was 91%. Cultured for three days, the percentages were 51% and medium control was 78%. Cultured for five days, the percentage was 53% and medium control was 81%. U937 cells were cultured in presence of rGM CSF (10 μg/L) for one day, the percentage of CD86 molecule expression was 2% and medium control was 1.6%. Cultured for three days, the percentages were 3.91% and medium control was 1%. Cultured for five days, the percentage was 5.32% and medium control was 0.58%. The percentage of MHC class Ⅰ molecule wxpression was 100% in presence of rGM CSF (10 μg/L) for five dyas and medium control was also 100%. The data show that rGM CSF dowm regulated DR and up regulated CD86 molecule expression, but did not alter MHC class Ⅰ molecule expression. MHC and CD86 molecules provide a stimulatory signal necessary for T cell activation. These results suggested the role of rGM CSF in immune regulation.
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