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体内CD4+ T细胞分泌白细胞介素-2迅速、短暂,并受TCR特异性竞争的影响。

IL-2 secretion by CD4+ T cells in vivo is rapid, transient, and influenced by TCR-specific competition.

作者信息

Sojka Dorothy K, Bruniquel Denis, Schwartz Ronald H, Singh Nevil J

机构信息

Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

J Immunol. 2004 May 15;172(10):6136-43. doi: 10.4049/jimmunol.172.10.6136.

Abstract

The secretion of IL-2 is a critical and early landmark in the activation program of CD4(+) T cells in vitro, but the lack of sensitive assays has limited its application for studying T cell activation in vivo. Using a mouse cytokine capture assay we were able to detect the rapid secretion of IL-2 after an in vivo stimulus by 1-2 h in naive T cells and as early as 30 min in memory T cells. Maximal secretion was achieved within 1-2 h for memory cells or 6-8 h for naive T cells. Surprisingly IL-2 production terminated quickly in vivo and secretion was undetectable by 20-24 h in either cell type. We further demonstrated that this short duration of secretion can be influenced by cellular competition between Ag-specific CD4(+) T cells. The consequences of competition were mimicked by reducing the strength of the antigenic stimulus. These data argue that early competition between T cells influences both the eventual frequency of IL-2 producers in the population and also the duration of their secretion, potentially by altering the strength or duration of the stimulus available to each T cell.

摘要

白细胞介素-2(IL-2)的分泌是体外CD4(+) T细胞激活程序中的一个关键且早期的标志,但由于缺乏灵敏的检测方法,限制了其在体内研究T细胞激活的应用。使用小鼠细胞因子捕获检测法,我们能够在体内刺激后1-2小时检测到初始T细胞中IL-2的快速分泌,而记忆T细胞中最早在30分钟就能检测到。记忆细胞在1-2小时内达到最大分泌量,初始T细胞则在6-8小时达到最大分泌量。令人惊讶的是,IL-2在体内的产生迅速终止,在20-24小时后,两种细胞类型中均检测不到其分泌。我们进一步证明,这种短暂的分泌持续时间会受到抗原特异性CD4(+) T细胞之间细胞竞争的影响。通过降低抗原刺激的强度可以模拟竞争的后果。这些数据表明,T细胞之间的早期竞争会影响群体中IL-2产生细胞的最终频率及其分泌持续时间,可能是通过改变每个T细胞可获得的刺激强度或持续时间来实现的。

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