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由Src家族激酶介导的TCR信号对于初始T细胞的存活至关重要。

TCR signals mediated by Src family kinases are essential for the survival of naive T cells.

作者信息

Seddon Benedict, Zamoyska Rose

机构信息

Division of Molecular Immunology, National Institute for Medical Research, The Ridgeway, London, United Kingdom.

出版信息

J Immunol. 2002 Sep 15;169(6):2997-3005. doi: 10.4049/jimmunol.169.6.2997.

Abstract

The role of TCR signals triggered by recognition of self MHCs in maintaining the survival of naive peripheral T cells remains controversial. Here we examine the role of the Src family kinases, p56(lck) (Lck) and p59(fyn) (Fyn), in the survival of naive T cells. We show that long term survival requires a combination of signals transduced by Src family kinases and signals through the IL-7R. In the absence of either one, naive T cells die slowly, but if both signals are removed, cell loss is greatly accelerated. The TCR signal can be mediated by either Fyn or Lck at wild-type levels of expression, but not by Lck alone if expressed suboptimally. The disappearance of T cells in the absence of Fyn and Lck was associated with a complete loss of TCRzeta-chain phosphorylation and down-regulation of CD5, both of which are also MHC contact dependent, indicating that the Src family kinases are critical for transducing a TCR-MHC survival signal.

摘要

由识别自身主要组织相容性复合体(MHC)所触发的T细胞受体(TCR)信号在维持外周幼稚T细胞存活中的作用仍存在争议。在此,我们研究了Src家族激酶p56(lck)(Lck)和p59(fyn)(Fyn)在幼稚T细胞存活中的作用。我们发现长期存活需要Src家族激酶转导的信号与通过白细胞介素-7受体(IL-7R)的信号相结合。若缺少其中任何一种信号,幼稚T细胞会缓慢死亡,但如果两种信号都缺失,细胞损失会大大加速。在野生型表达水平下,TCR信号可由Fyn或Lck介导,但如果Lck表达水平次优,则不能单独介导。在缺少Fyn和Lck的情况下T细胞消失与TCRζ链磷酸化的完全丧失以及CD5的下调有关,这两者也都依赖于MHC接触,表明Src家族激酶对于转导TCR-MHC存活信号至关重要。

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