Immunological Synapse Formation Licenses CD40-CD40L Accumulations at T-APC Contact Sites
Author(s) -
Judie Boisvert,
Samuel Edmondson,
Matthew F. Krummel
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.173.6.3647
Subject(s) - immunological synapse , t cell receptor , cd154 , microbiology and biotechnology , t cell , receptor , cd3 , cd40 , ligand (biochemistry) , synapse , integrin , chemistry , biology , cd8 , cytotoxic t cell , immunology , antigen , neuroscience , immune system , biochemistry , in vitro
The maintenance of tolerance is likely to rely on the ability of a T cell to polarize surface molecules providing "help" to only specific APCs. The formation of a mature immunological synapse leads to concentration of the TCR at the APC interface. In this study, we show that the CD40-CD154 receptor-ligand pair is also highly concentrated into a central region of the synapse on mouse lymphocytes only after the formation of the TCR/CD3 c-SMAC. Concentration of this ligand was strictly dependent on TCR recognition, the binding of ICAM-1 to T cell integrins and the presence of an intact cytoskeleton in the T cells. This may provide a novel explanation for the specificity of T cell help directing the help signal to the site of Ag receptor signal. It may also serve as a site for these molecular aggregates to coassociate and/or internalize alongside other signaling receptors.
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