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作 者:魏明[1] 甘露[2] 侯进[1] 陈丽宏[2] 刘彦彤[3] 任立刚[3]
机构地区:[1]西安医学院药理学教研室,陕西西安710021 [2]陕西省人民医院妇科,陕西西安710068 [3]西安医学院生物化学与分子生物学教研室,陕西西安710021
出 处:《细胞与分子免疫学杂志》2016年第12期1641-1645,共5页Chinese Journal of Cellular and Molecular Immunology
基 金:陕西省自然科学基础研究(2016JM8046;2014JQ2-8055;2016JM8047);西安医学院校级重点建设学科资助项目(2015097);陕西省卫计委重点项目(2014A)
摘 要:目的探讨(Pyr^1)apelin-13对Jurkat T淋巴细胞增殖和活化的影响。方法用(0、10、50)nmol/L(Pyr^1)apelin-13处理Jurkat T淋巴细胞24 h后,用CCK-8法检测细胞增殖能力的变化;用抗CD3抗体和抗CD28抗体包被并活化Jurkat T淋巴细胞,观察(Pyr^1)apelin-13对Jurkat T淋巴细胞活化的影响;实时定量PCR检测CD69、CD25、细胞毒性T淋巴细胞相关蛋白4(CTLA-4)及程序性死亡蛋白1(PD-1)的mRNA水平。结果 (Pyr^1)apelin-13对Jurkat T淋巴细胞增殖无影响,但通过增加CD69和CD25的表达促进Jurkat T淋巴细胞活化,但对CTLA-4和PD-1表达影响不明显。结论 (Pyr^1)apelin-13促进Jurkat T淋巴细胞活化。Objective To investigate the effect of (Pyr1 ) apelin-13 on the proliferation and activation of Jurkat T lymphocytes. Methods Jurkat T cells were treated by 0, 10, 50 nmol/L (Pyr1) apelin-13 for 24 hours and cell proliferation ability was detected by CCK-8 assay. The effect of ( PyrI ) apelin-13 on the activation of Jurkat T lymphocytes with anti-CD3 and anti-CD28 antibodies was observed and the molecular mechanism was investigated. Quantitative real-time PCR was applied to detect the expressions of CD69, CD25, cytotoxic T lymphocyte antigen-4 (CTLA-4) and programmed death-t ( PD-1 ) mRNAs. Results The proliferation of Jurkat T cells was not affected by (Pyr1) apelin-13. However, (Pyr1) apelin-13 increased the expressions of CD69 and CD25 and then activated Jurkat T lymphocytes. Furthermore, the expressions of CTLA-4 and PD-] had no difference between activation group and ( Pyrt ) apelin-13 group. Conclusion ( Pyr1 ) apelin-13 promotes Jurkat T lymphocyte activation by increasing the expressions of CD69 and CD25.
关 键 词:(Pyr1)apelin-13 T淋巴细胞活化 CD69 CD25
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