TAOK3, a Regulator of LCK-SHP-1 Crosstalk during TCR Signaling

被引:5
|
作者
Ormonde, Joao V. S. [1 ,2 ,3 ]
Nie, Yan [4 ]
Madrenas, Joaquin [1 ,2 ,3 ]
机构
[1] Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Torrance, CA 90509 USA
[2] McGill Univ, Microbiome & Dis Tolerance Ctr, Montreal, PQ, Canada
[3] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
[4] McGill Univ, Dept Biochem, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
T cell activation; signal transduction; TCR signaling regulation; LCK; SHP-1; TAOK3; T-CELL-RECEPTOR; 20-LIKE KINASES PSKS/TAOKS; GENOME-WIDE ASSOCIATION; PROTEIN-KINASE; TYROSINE-PHOSPHATASE; NEGATIVE REGULATION; POSITIVE SELECTION; ACTIVATION; LCK; SHP-1;
D O I
10.1615/CritRevImmunol.2019030480
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Signaling from the T cell receptor for antigen turns on the physiological response of a T cell. The canonical TCR signaling pathway relies on early activation of the Src kinase LCK. This step initiates a cascade of events that lead not only to the phenotypic changes that characterize effector T cells but also to the activation of negative regulatory mechanisms that stop early TCR signaling. These mechanisms ensure qualitative and quantitative fine-tuning of T cell activation. The tyrosine phosphatase SHP-1 is a key player in the downregulation of LCK activation. In this review, we focus on the crosstalk between LCK and SHP-1 and, based on recent data, we introduce the putative kinase TAOK3 as an important regulator of this crosstalk. Given the widespread expression of TAOK3 and SHP-1, we propose that the function of TAOK3 extends beyond T cells and may be fundamental in the regulation of early signaling from receptors that utilize Src kinases.
引用
收藏
页码:59 / 81
页数:23
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