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

被引:49
作者
Lu, Yan [1 ]
Zhong, Ming-Chao [1 ]
Qian, Jin [1 ]
Calderon, Virginie [2 ]
Tleugabulova, Mayra Cruz [3 ]
Mallevaey, Thierry [3 ,4 ]
Veillette, Andre [1 ,5 ,6 ]
机构
[1] Inst Rech Clin Montreal, Lab Mol Oncol, Montreal, PQ, Canada
[2] Inst Rech Clin Montreal, Bioinformat Core Facil, Montreal, PQ, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON, Canada
[4] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON, Canada
[5] Univ Montreal, Dept Med, Montreal, PQ, Canada
[6] McGill Univ, Dept Med, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
KILLER T-CELLS; FAMILY RECEPTORS; SAP ADAPTERS; LY108; ACTIVATION; MICE; EXPRESSION; INDUCTION; DELETION; IMMUNITY;
D O I
10.1038/s41590-019-0334-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Invariant natural killer T cells (iNKT cells) develop through an incompletely understood process that requires positive selection by CD4(+) CD8(+) 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.
引用
收藏
页码:447 / +
页数:13
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