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SLAM 受体通过降低阳性选择后 TCR 信号强度促进 iNKT 细胞发育。

SLAM receptors foster iNKT cell development by reducing TCR signal strength after positive selection.

机构信息

Laboratory of Molecular Oncology, Institut de recherches cliniques de Montréal, Montréal, Québec, Canada.

Bioinformatics Core Facility, Institut de recherches cliniques de Montréal, Montréal, Québec, Canada.

出版信息

Nat Immunol. 2019 Apr;20(4):447-457. doi: 10.1038/s41590-019-0334-0. Epub 2019 Mar 4.

Abstract

Invariant natural killer T cells (iNKT cells) develop through an incompletely understood process that requires positive selection by CD4CD8 double-positive thymocytes and SLAM family receptors (SFRs). Here we found that SFRs promoted the development of iNKT cells by reducing the strength of the T cell antigen receptor (TCR) signal after positive selection. This effect improved the survival of iNKT cells and their responses to antigen. Loss of SFRs upregulated the expression of inhibitory receptors, including PD-1, on iNKT cells to mitigate the deleterious effect of SFR deficiency. The role of SFRs could be mimicked by expression of SLAMF6 alone in SFR-deficient mice, and this involved the adaptor SAP-kinase Fyn complex and the phosphatase SHP-1. Thus, SFRs foster iNKT cell development by attenuating TCR signal strength after positive selection.

摘要

不变自然杀伤 T 细胞 (iNKT 细胞) 通过一个尚未完全了解的过程发育,该过程需要 CD4CD8 双阳性胸腺细胞和 SLAM 家族受体 (SFRs) 的阳性选择。在这里,我们发现 SFRs 通过降低阳性选择后 T 细胞抗原受体 (TCR) 信号的强度来促进 iNKT 细胞的发育。这种作用改善了 iNKT 细胞的存活及其对抗原的反应。SFR 的缺失上调了抑制性受体的表达,包括 PD-1,以减轻 SFR 缺乏的有害影响。SFR 缺陷小鼠中单独表达 SLAMF6 即可模拟 SFR 的作用,这涉及衔接子 SAP 激酶 Fyn 复合物和磷酸酶 SHP-1。因此,SFRs 通过在阳性选择后减弱 TCR 信号强度来促进 iNKT 细胞的发育。

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