RIBP, a novel R1k/Txk- and Itk-binding adaptor protein that regulates T cell activation

被引:77
作者
Rajagopal, K
Sommers, CL
Decker, DC
Mitchell, EO
Korthauer, U
Sperling, AI
Kozak, CA
Love, PE
Bluestone, JA
机构
[1] Univ Chicago, Ben May Inst Canc Res, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Med, Pulm & Crit Care Med Sect, Chicago, IL 60637 USA
[3] NIAID, Mol Microbiol Lab, NIH, Bethesda, MD 20892 USA
[4] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[5] NICHHD, Lab Mammalian Genes & Dev, NIH, Bethesda, MD 20892 USA
关键词
T cell activation; signal transduction; adaptor protein; Tec tyrosine kinases; T helper type 1/T helper type 2 cells;
D O I
10.1084/jem.190.11.1657
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A novel T cell-specific adaptor protein, RIBP, was identified based on its ability to bind Rlk/Txk in a yeast two-hybrid screen of a mouse T cell lymphoma library. RIBP was also found to interact with a related member of the Tec family of tyrosine kinases, Itk. Expression of RIBP is restricted to T and natural killer cells and is upregulated substantially after T cell activation. RIBP-disrupted knockout mice displayed apparently normal T cell development. However, proliferation of RIBP-deficient T cells in response to T cell receptor (TCR)-mediated activation was significantly impaired. Furthermore, these activated T cells were defective in the production of interleukin (IL)-2 and interferon gamma, but not IL-4. These data suggest that RIBP plays an important role in TCR-mediated signal transduction pathways and that its binding to Itk and Rlk/Txk may regulate T cell differentiation.
引用
收藏
页码:1657 / 1668
页数:12
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