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Early T Cell Activation in Elderly Humans

机译:老年人的早期T细胞活化

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This study characterizes the early steps of T lymphocyte activation in healthy elderly subjects. The expression of CD69, the earliest inducible antigen which appears with T lymphocyte activation, was assessed in T cells cultured with medium, anti-CD3 or PMA. The proliferative responses of T cells stimulated through CD69 and CD3 pathways were also studied. Donors included 31 healthy elderly [age mean (SD) 80(8) years] and 33 healthy young [age 30(5) years] subjects. In elderly people, the expression of CD69 was lower in T cells cultured with medium [3.4% (1.65-5.9; 25-75 percentiles) vs. 10% (6-18), p < 0.0003] and anti-CD3 activated [28.1% (16.5-53.8) vs. 79.5% (73-89), p < 0.0002] T cells. With PMA at 10 ng/ml, CD69 expression was higher in both groups of T cells, though still lower in the aged [84.5% (70.9-94.9) vs. 99% (65.7-100), p = 0.051]. CD69 T cell expression was equal in both groups with 2 ng/ml of PMA, but the co-stimulatory responses to CD69 under these conditions and in the presence of anti-CD3 were lower in the aged (16914 vs. 28904 cpm, p < 0.02) and (6944 vs. 14370 cpm, p < 0.02) respectively. Aged T cells failed to express CD25 at the same levels of young T cells when stimulated with CD69. These results suggest an age-associated defect in the very early steps of T lymphocyte activation that might influence later stages of lymphocyte function. An alteration in the transmission of the activation signal from the cell surface to protein kinase C may play a primary role in this defect.
机译:这项研究表征了健康老年受试者中T淋巴细胞活化的早期步骤。在用培养基,抗CD3或PMA培养的T细胞中评估了CD69的表达,CD69是最早出现的T淋巴细胞活化的可诱导抗原。还研究了通过CD69和CD3途径刺激的T细胞的增殖反应。捐赠者包括31名健康的老年人[平均年龄(SD)80(8)岁]和33名健康的年轻[年龄30(5)岁]受试者。在老年人中,用培养基培养的T细胞中CD69的表达较低[3.4%(1.65-5.9; 25-75%),而10%(6-18),p <0.0003],并且抗CD3被激活[28.1 %(16.5-53.8)对79.5%(73-89),p <0.0002] T细胞。当PMA为10 ng / ml时,两组T细胞中CD69的表达均较高,但在老年人中仍较低[84.5%(70.9-94.9)对99%(65.7-100),p = 0.051]。两组中,使用2 ng / ml PMA的两组中CD69 T细胞表达均相等,但在这些条件下以及存在抗CD3的情况下,老年人中对CD69的共刺激反应较低(16914 vs. 28904 cpm,p < 0.02)和(6944 vs. 14370 cpm,p <0.02)。当用CD69刺激时,老化的T细胞无法以相同水平的年轻T细胞表达CD25。这些结果表明,T淋巴细胞活化的早期阶段存在与年龄相关的缺陷,这可能会影响淋巴细胞功能的后期阶段。激活信号从细胞表面到蛋白激酶C的传递改变可能在此缺陷中起主要作用。

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