Abstract
The specialized junction between a T lymphocyte and an antigen-presenting cell, the immunological synapse, consists of a central cluster of T cell receptors surrounded by a ring of adhesion molecules. Immunological synapse formation is now shown to be an active and dynamic mechanism that allows T cells to distinguish potential antigenic ligands. Initially, T cell receptor ligands were engaged in an outermost ring of the nascent synapse. Transport of these complexes into the central cluster was dependent on T cell receptor-ligand interaction kinetics. Finally, formation of a stable central cluster at the heart of the synapse was a determinative event for T cell proliferation.
Publication types
-
Research Support, Non-U.S. Gov't
-
Research Support, U.S. Gov't, P.H.S.
MeSH terms
-
Animals
-
Antigen-Presenting Cells / immunology
-
Antigen-Presenting Cells / metabolism
-
CD4 Antigens / immunology
-
CD4 Antigens / metabolism
-
CHO Cells
-
Cell Movement
-
Cricetinae
-
Cytochrome c Group / immunology
-
Cytochrome c Group / metabolism
-
Fluorescence
-
Histocompatibility Antigens / immunology
-
Histocompatibility Antigens / metabolism*
-
Intercellular Adhesion Molecule-1 / immunology
-
Intercellular Adhesion Molecule-1 / metabolism
-
Ligands
-
Lipid Bilayers
-
Lymphocyte Activation*
-
Mice
-
Mice, Transgenic
-
Microscopy, Interference
-
Models, Immunological
-
Peptides / immunology
-
Peptides / metabolism
-
Receptors, Antigen, T-Cell / immunology
-
Receptors, Antigen, T-Cell / metabolism*
-
Signal Transduction
-
T-Lymphocytes / immunology*
-
T-Lymphocytes / metabolism
-
Time Factors
Substances
-
CD4 Antigens
-
Cytochrome c Group
-
Histocompatibility Antigens
-
Ligands
-
Lipid Bilayers
-
Peptides
-
Receptors, Antigen, T-Cell
-
Intercellular Adhesion Molecule-1