THEMIS enhances TCR signaling and enables positive selection by selective inhibition of the phosphatase SHP-1

被引:65
作者
Choi, Seeyoung [1 ]
Warzecha, Claude [1 ]
Zvezdova, Ekaterina [1 ]
Lee, Jan [1 ]
Argenty, Jeremy [2 ,3 ,4 ]
Lesourne, Renaud [2 ,3 ,4 ]
Aravind, L. [5 ]
Love, Paul E. [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Hematopoiesis & Lymphocyte Biol, NIH, Bethesda, MD 20892 USA
[2] Ctr Physiopathol Toulouse Purpan, Toulouse, France
[3] CNRS, INSERM, U1043, U5282, Toulouse, France
[4] Univ Paul Sabatier, Univ Toulouse, Toulouse, France
[5] NIH, Natl Lib Med, Bldg 10, Bethesda, MD 20892 USA
关键词
PROTEIN-TYROSINE PHOSPHATASES; T-CELL DEVELOPMENT; THYMOCYTE DEVELOPMENT; RECEPTOR STIMULATION; NEGATIVE SELECTION; REDOX REGULATION; ACTIVATION; GENERATION; DELETION; STRENGTH;
D O I
10.1038/ni.3692
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
THEMIS, a T cell-specific protein with high expression in CD4(+)CD8(+) thymocytes, has a crucial role in positive selection and T cell development. THEMIS lacks defined catalytic domains but contains two tandem repeats of a distinctive module of unknown function (CABIT). Here we found that THEMIS directly regulated the catalytic activity of the tyrosine phosphatase SHP-1. This action was mediated by the CABIT modules, which bound to the phosphatase domain of SHP-1 and promoted or stabilized oxidation of SHP-1's catalytic cysteine residue, which inhibited the tyrosine-phosphatase activity of SHP-1. Deletion of SHP-1 alleviated the developmental block in Themis(-/-) thymocytes. Thus, THEMIS facilitates thymocyte positive selection by enhancing the T cell antigen receptor signaling response to low-affinity ligands.
引用
收藏
页码:433 / +
页数:10
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