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NKT Cell-TCR Expression Activates Conventional T Cells in Vivo but Is Largely Dispensable for Mature NKT Cell Biology

机译:NKT细胞-TCR表达激活体内的常规T细胞但对于成熟的NKT细胞生物学却大有可为

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摘要

Natural killer T (NKT) cell development depends on recognition of self-glycolipids via their semi-invariant Vα14i-TCR. However, to what extent TCR-mediated signals determine identity and function of mature NKT cells remains incompletely understood. To address this issue, we developed a mouse strain allowing conditional Vα14i-TCR expression from within the endogenous Tcrα locus. We demonstrate that naïve T cells are activated upon replacement of their endogenous TCR repertoire with Vα14i-restricted TCRs, but they do not differentiate into NKT cells. On the other hand, induced TCR ablation on mature NKT cells did not affect their lineage identity, homeostasis, or innate rapid cytokine secretion abilities. We therefore propose that peripheral NKT cells become unresponsive to and thus are independent of their autoreactive TCR.
机译:天然杀伤性T细胞(NKT)的发育取决于通过半不变的Vα14i-TCR对自身糖脂的识别。但是,TCR介导的信号在多大程度上决定了成熟NKT细胞的身份和功能尚不完全清楚。为了解决这个问题,我们开发了一种小鼠品系,可从内源性Tcrα基因座内条件表达Vα14i-TCR。我们证明,用Vα14i限制性TCR替换其内源性TCR库后,会激活幼稚T细胞,但它们不会分化为NKT细胞。另一方面,在成熟的NKT细胞上诱导的TCR消融并不影响其谱系同一性,体内稳态或先天性快速细胞因子分泌能力。因此,我们提出外周NKT细胞变得无反应,因此独立于其自身反应性TCR。

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