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L-2 and IL-15 dependent thymic development of Foxp3-expressing regulatory T lymphocytes 被引量:6
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作者 Cecile Apert Paola Romagnoli Joost P, M. van Meerwijk 《Protein & Cell》 SCIE CAS CSCD 2018年第4期322-332,共11页
Immunosuppressive regulatory T lymphocytes (Treg) expressing the transcription factor Foxp3 play a vital role in the maintenance of tolerance of the immune-system to self and innocuous non-self. Most Treg that are c... Immunosuppressive regulatory T lymphocytes (Treg) expressing the transcription factor Foxp3 play a vital role in the maintenance of tolerance of the immune-system to self and innocuous non-self. Most Treg that are critical for the maintenance of tolerance to self, develop as an independent T-cell lineage from common T cell precursors in the thymus. In this organ, their differentiation requires signals from the T cell receptor for antigen, from co-stimulatory molecules, as well as from cytokine-receptors. Here we focus on the cytokines implicated in thymic development of Treg, with a particular emphasis on the roles of interleukin-2 (IL-2) and IL-15. The more recently appreciated involvement of TGF-β in thymic Treg development is also briefly discussed. Finally, we discuss how cytokine-dependence of Treg development allows for temporal, quantitative, and potentially qualitative modulation of this process. 展开更多
关键词 regulatory t cells tHYMUS differentiation il-2 il-15
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晚期氧化蛋白产物抑制CD4+CD25-T细胞向CD4+CD25+调节性T细胞转化 被引量:3
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作者 李凯 白晓峰 +4 位作者 冯梅 石华 王元林 孙兆林 徐述雄 《中华实验外科杂志》 CAS CSCD 北大核心 2018年第10期1902-1904,共3页
目的探讨晚期氧化蛋白产物(AOPP)对CD4+CD25-T细胞向CD4+CD25-T调节性T细胞(Tregs)转化的影响及机制。方法将CD4+CD25-T细胞按1×10^6/孔培养于平底96孔板,依据是否加入AOPP分为3组:对照组(加入人血清白蛋白200μg/m1)... 目的探讨晚期氧化蛋白产物(AOPP)对CD4+CD25-T细胞向CD4+CD25-T调节性T细胞(Tregs)转化的影响及机制。方法将CD4+CD25-T细胞按1×10^6/孔培养于平底96孔板,依据是否加入AOPP分为3组:对照组(加入人血清白蛋白200μg/m1);AOPP组(加入AOPP200μg/m1);抗氧化组(DPI100μmol/L预处理1h后再加入AOPP200μg/m1)。流式细胞仪检测各组细胞表型变化和DHE荧光强度,3H-TdR掺入法检测Tregs对效应T细胞(Teff)的免疫抑制功能,West-ernblot法检测细胞内磷酸化信号转导与转录激活因子5(p-STAT5)的变化。结果AOPP组中CD4+CD25+T细胞占(28.6±4.5)%、胞内因子Foxp3在CD4+CD25+T细胞中的表达率为(10.7±1.7)%,显著低于对照组细胞的相应值(73.8±10.7)%、(64.3±9.4)%(P=0.003,0.001);抗氧化组细胞表型分别为(41.3±4.6.4)%、(22.3±3.0)%,转化较AOPP组多(P=0.049,0.004),低于对照组(P=0.011,0.002)。在Tregs:Teff为1:1的情况下,AOPP组Teff的每分钟脉冲数值(CPM)为17521.0±1703.8,显著高于对照组的9932.3±1142.9(P=0.003);抗氧化组的Teff的CPM为15709.7±1272.9,高于对照组(P=0.004),但与AOPP组比较差异无统计学意义(P=0.214)。AOPP组DHE荧光强度为(163.0±11.5)%,较对照组(51.1±4.0)%高(P=0.000);而抗氧化组DHE荧光强度(113.4±7.8)%较AOPP组低(P=0.003),高于对照组(P=0.000)。AOPP组p-STAT5表达较对照组低(P=0.006);而抗氧化组p-STAT5表达较AOPP组显著性上调(P=0.008),但仍低于对照组(P=0.043)。结论AOPP抑制CD4+CD25-T细胞向Tregs转化,其机制可能是通过氧化应激下调p-STAT5的表达。 展开更多
关键词 晚期氧化蛋白产物 白细胞介素.15 调节性t细胞 t细胞 磷酸化信号转 导与转录激活因子5
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