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幼稚 T 细胞成熟依赖性许可快速产生 TNF。

Maturation-dependent licensing of naive T cells for rapid TNF production.

机构信息

Department of Pathology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

出版信息

PLoS One. 2010 Nov 24;5(11):e15038. doi: 10.1371/journal.pone.0015038.

Abstract

The peripheral naïve T cell pool is comprised of a heterogeneous population of cells at various stages of development, which is a process that begins in the thymus and is completed after a post-thymic maturation phase in the periphery. One hallmark of naïve T cells in secondary lymphoid organs is their unique ability to produce TNF rapidly after activation and prior to acquiring other effector functions. To determine how maturation influences the licensing of naïve T cells to produce TNF, we compared cytokine profiles of CD4(+) and CD8(+) single positive (SP) thymocytes, recent thymic emigrants (RTEs) and mature-naïve (MN) T cells during TCR activation. SP thymocytes exhibited a poor ability to produce TNF when compared to splenic T cells despite expressing similar TCR levels and possessing comparable activation kinetics (upregulation of CD25 and CD69). Provision of optimal antigen presenting cells from the spleen did not fully enable SP thymocytes to produce TNF, suggesting an intrinsic defect in their ability to produce TNF efficiently. Using a thymocyte adoptive transfer model, we demonstrate that the ability of T cells to produce TNF increases progressively with time in the periphery as a function of their maturation state. RTEs that were identified in NG-BAC transgenic mice by the expression of GFP showed a significantly enhanced ability to express TNF relative to SP thymocytes but not to the extent of fully MN T cells. Together, these findings suggest that TNF expression by naïve T cells is regulated via a gradual licensing process that requires functional maturation in peripheral lymphoid organs.

摘要

外周初始 T 细胞池由处于不同发育阶段的异质性细胞群组成,这个过程始于胸腺,并在胸腺后成熟阶段在外周完成。次级淋巴器官中初始 T 细胞的一个标志特征是,它们在获得其他效应功能之前,在激活后能够迅速产生 TNF。为了确定成熟如何影响初始 T 细胞产生 TNF 的许可,我们比较了 TCR 激活过程中 CD4(+)和 CD8(+)单阳性 (SP) 胸腺细胞、近期胸腺迁出细胞 (RTE) 和成熟-初始 (MN) T 细胞的细胞因子谱。尽管 SP 胸腺细胞表达相似的 TCR 水平并具有相似的激活动力学(CD25 和 CD69 的上调),但与脾 T 细胞相比,它们产生 TNF 的能力很差。从脾提供最佳的抗原呈递细胞并不能使 SP 胸腺细胞完全产生 TNF,这表明它们有效产生 TNF 的能力存在内在缺陷。通过胸腺细胞过继转移模型,我们证明 T 细胞在周围环境中产生 TNF 的能力随着时间的推移而逐渐增加,这是其成熟状态的函数。通过 NG-BAC 转基因小鼠中 GFP 的表达鉴定的 RTE 与 SP 胸腺细胞相比,表达 TNF 的能力显著增强,但不如完全 MN T 细胞。这些发现表明,初始 T 细胞中 TNF 的表达受一个逐渐许可过程的调节,该过程需要外周淋巴器官中的功能成熟。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1734/2991336/26e61e3f4003/pone.0015038.g001.jpg

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