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Foxp3 在人类和小鼠胸腺中的诱导发生在 CD4+ CD8+ 阶段之前,但需要早期 T 细胞受体表达。

Foxp3 induction in human and murine thymus precedes the CD4+ CD8+ stage but requires early T-cell receptor expression.

机构信息

Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.

出版信息

Immunol Cell Biol. 2010 Jul;88(5):523-8. doi: 10.1038/icb.2010.4. Epub 2010 Feb 9.

Abstract

The thymus generates a T-cell lineage dedicated to immune regulation, 'naturally occurring' regulatory T cells, best specified by the forkhead family transcription factor Foxp3. Here, we have conducted a parallel study in humans and mice where we have dissected the earliest stages of Foxp3 induction during thymocyte development. By analyzing a large collection of 21 human thymuses we show that Foxp3 can be consistently detected in CD4 immature single positive thymocytes that precede the CD4(+)CD8(+) (double positive, DP) stage. The reduced levels of CD3 expression found at this stage of human thymocyte development raise the question of TCR (T-cell receptor) requirement for Foxp3 induction. We further show that, in mice, Foxp3 expression was also detected in pre-DP thymocytes of TCRalpha-sufficient but not in TCRalpha-deficient animals, genetically showing the TCR dependence of Foxp3 expression at pre-DP stages of T-cell development.

摘要

胸腺产生了一种专门用于免疫调节的 T 细胞谱系,即“天然存在”的调节性 T 细胞,其特征最好由叉头框家族转录因子 Foxp3 来指定。在这里,我们在人类和小鼠中进行了平行研究,剖析了胸腺细胞发育过程中 Foxp3 诱导的最早阶段。通过分析 21 个人类胸腺的大量样本,我们表明 Foxp3 可以在 CD4 不成熟的单阳性胸腺细胞中持续检测到,这些细胞发生在 CD4(+)CD8(+)(双阳性,DP)阶段之前。在人类胸腺细胞发育的这一阶段发现 CD3 表达水平降低,这提出了 TCR(T 细胞受体)对 Foxp3 诱导的需求问题。我们进一步表明,在小鼠中,Foxp3 的表达也在 TCRalpha 充足的但不是在 TCRalpha 缺乏的动物的前 DP 胸腺细胞中检测到,从遗传学上显示了在 T 细胞发育的前 DP 阶段 TCR 对 Foxp3 表达的依赖性。

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