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PMID: 16473826 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Deconstructing the form and function of the TCR/CD3 complex.

Immunity ·Vol. 24 ·No. 2 ·2006-02-00 ·Pages 133-9

Kuhns MS, Davis MM, Garcia KC

Abstract

When T cells encounter antigens via the T cell antigen receptor (TCR), information about the quantity and quality of antigen engagement is relayed to the intracellular signal transduction machinery. This process is poorly understood. The TCR itself lacks a significant intracellular domain. Instead, it is associated with CD3 molecules that contain intracellular signaling domains that couple the TCR/CD3 complex to the downstream signaling machinery. The earliest events in TCR signaling must involve the transfer of information from the antigen binding TCR subunit to the CD3 signaling subunits of the TCR/CD3 complex. Elucidating the structural organization of the TCR with the associated CD3 signaling molecules is necessary for understanding the mechanism by which TCR engagement is coupled to activation. Here, we review the current state of our understanding of the structure and organization of the TCR/CD3 complex.

MeSH Terms
Animals Antigens, Differentiation, T-Lymphocyte/chemistry Cell Membrane/immunology Humans Models, Molecular Protein Conformation Receptor Cross-Talk Receptor-CD3 Complex, Antigen, T-Cell/chemistry,physiology Signal Transduction T-Lymphocytes/immunology
Chemicals
Antigens, Differentiation, T-Lymphocyte Receptor-CD3 Complex, Antigen, T-Cell
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kuhns Michael S
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305, USA.
Davis Mark M
Garcia K Christopher
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
2006-02-00
Pages
133-9
Language
English
Region
United States
NLM ID
9432918
Subset
IM
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