Abstract
The T cell, Ig domain, and mucin domain-1 (TIM-1) gene is associated with Th2 T cell responses and human atopic diseases. The mechanism by which TIM-1 influences T cell responses remains unknown. We demonstrate that TIM-1 is recruited to the TCR-signaling complex via association with CD3. TIM-1 up-regulates TCR-associated signaling events, including phosphorylation of Zap70 and IL-2-inducible T cell kinase. This activity requires TIM-1 tyrosine phosphorylation. TIM-1 expression induces formation of a novel complex that includes PI3K and ITK. Finally, the consequences of TIM-1 activation include increased expression of effector cytokines. These results demonstrate that TIM-1 is a critical component of the human T cell response and provide a mechanistic hypothesis for the role of TIM-1 in disease.
MeSH terms
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CD3 Complex / analysis
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CD3 Complex / metabolism*
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Cells, Cultured
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Cytokines / metabolism
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Hepatitis A Virus Cellular Receptor 1
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Humans
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Lymphocyte Activation*
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Membrane Glycoproteins / analysis
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Membrane Glycoproteins / genetics
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Membrane Glycoproteins / metabolism*
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Phosphatidylinositol 3-Kinases / metabolism
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Phosphorylation
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Protein-Tyrosine Kinases / metabolism
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Receptors, Antigen, T-Cell / metabolism*
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Receptors, Virus / analysis
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Receptors, Virus / genetics
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Receptors, Virus / metabolism*
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T-Lymphocytes / chemistry
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T-Lymphocytes / immunology*
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Tyrosine / genetics
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Tyrosine / metabolism
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Up-Regulation
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ZAP-70 Protein-Tyrosine Kinase / metabolism
Substances
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CD3 Complex
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Cytokines
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HAVCR1 protein, human
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Hepatitis A Virus Cellular Receptor 1
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Membrane Glycoproteins
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Receptors, Antigen, T-Cell
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Receptors, Virus
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Tyrosine
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Phosphatidylinositol 3-Kinases
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Protein-Tyrosine Kinases
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ZAP-70 Protein-Tyrosine Kinase
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ZAP70 protein, human
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emt protein-tyrosine kinase