Abstract
T cell activation in vivo occurs in a lymphoid milieu that presents chemotactic and T cell receptor signals concurrently. Here we demonstrate that T cell zone chemokines such as CCL21 are bound to the surface of lymph node dendritic cells. Contact with antigen-presenting cells bearing chemokines costimulated T cells by a previously unknown two-step contact mechanism. T cells initially formed an antigen-independent 'tethered' adhesion on chemokine-bearing antigen-presenting cells. The formation of those tethers superseded T cell receptor signaling and immunological synapse formation. However, chemokine-tethered T cells were hyper-responsive to subsequent contacts with antigen-presenting cells. Thus, T cells are costimulated 'in trans' and sequentially after initial engagement with their chemokine-rich environment.
MeSH terms
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Animals
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Antigen-Presenting Cells / immunology*
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Antigens, CD / metabolism
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Cell Adhesion
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Cell Adhesion Molecules / metabolism
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Cell Communication / immunology*
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Chemokine CCL21
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Chemokines / immunology*
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Chemokines / pharmacology
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Chemokines, CC / analysis
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Chemokines, CC / pharmacology
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Dendritic Cells / immunology*
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Intercellular Adhesion Molecule-1 / metabolism
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Ligands
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Lymph Nodes / cytology
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Lymph Nodes / immunology
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Lymphocyte Activation
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Lymphocyte Function-Associated Antigen-1 / metabolism
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Mice
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Mice, Inbred Strains
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Mice, Mutant Strains
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Receptors, CCR7
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Receptors, Chemokine / genetics
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Receptors, Chemokine / metabolism
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T-Lymphocytes / drug effects
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T-Lymphocytes / immunology*
Substances
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Antigens, CD
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Ccl21c protein, mouse
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Ccr7 protein, mouse
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Cell Adhesion Molecules
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Chemokine CCL21
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Chemokines
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Chemokines, CC
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ICAM-2 protein, mouse
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Icam1 protein, mouse
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Ligands
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Lymphocyte Function-Associated Antigen-1
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Receptors, CCR7
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Receptors, Chemokine
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Intercellular Adhesion Molecule-1