Role of CD3 gamma in T cell receptor assembly

J Dietrich, A Neisig, X Hou, A M Wegener, M Gajhede, C Geisler

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Abstract

The T cell receptor (TCR) consists of the Ti alpha beta heterodimer and the associated CD3 gamma delta epsilon and zeta 2 chains. The structural relationships between the subunits of the TCR complex are still not fully known. In this study we examined the role of the extracellular (EC), transmembrane (TM), and cytoplasmic (CY) domain of CD3 gamma in assembly and cell surface expression of the complete TCR in human T cells. A computer model indicated that the EC domain of CD3 gamma folds as an Ig domain. Based on this model and on alignment studies, two potential interaction sites were predicted in the EC domain of CD3 gamma. Site-directed mutagenesis demonstrated that these sites play a crucial role in TCR assembly probably by binding to CD3 epsilon. Mutagenesis of N-linked glycosylation sites showed that glycosylation of CD3 gamma is not required for TCR assembly and expression. In contrast, treatment of T cells with tunicamycin suggested that N-linked glycosylation of CD3 delta is required for TCR assembly. Site-directed mutagenesis of the acidic amino acid in the TM domain of CD3 gamma demonstrated that this residue is involved in TCR assembly probably by binding to Ti beta. Deletion of the entire CY domain of CD3 gamma did not prevent assembly and expression of the TCR. In conclusion, this study demonstrated that specific TCR interaction sites exist in both the EC and TM domain of CD3 gamma. Furthermore, the study indicated that, in contrast to CD3 gamma, glycosylation of CD3 delta is required for TCR assembly and expression.
Original languageEnglish
JournalJournal of Cell Biology
Volume132
Issue number3
Pages (from-to)299-310
Number of pages11
ISSN0021-9525
Publication statusPublished - 1996

Bibliographical note

Keywords: Amino Acid Sequence; Animals; Antigens, CD3; Birds; Cell Membrane; Computer Simulation; Cytosol; Humans; Macromolecular Substances; Mice; Models, Molecular; Models, Structural; Molecular Sequence Data; Protein Folding; Protein Structure, Secondary; Rats; Receptor-CD3 Complex, Antigen, T-Cell; Receptors, Antigen, T-Cell, alpha-beta; Receptors, Antigen, T-Cell, gamma-delta; Sequence Homology, Amino Acid; Sheep; T-Lymphocytes

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