Binding of phosphatidyl-inositol-3-OH kinase to CD28 is required for T-cell signalling View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1994-05

AUTHORS

Françoise Pagès, Marguerite Ragueneau, Robert Rottapel, Alemseged Truneh, Jacques Nunes, Jean Imbert, Daniel Olive

ABSTRACT

THE engagement of CD28 with its ligand B7.1/CD80 results in potent costimulation of T-cell activation initiated through the CD3/T-cell receptor complex1,2. The biochemical basis of CD28 costimulatory function is poorly understood. The signalling pathways used by CD28 are unlike those used by the CD3/T-cell receptor in that they are resistant to cyclosporin A and independent of changes in cyclic AMP concentrations3. These differences suggest that each pathway provides unique biochemical informa-tion which is required for T-cell activation. We report here that CD28 becomes tyrosine-phosphorylated following interaction with B7.1/CD80, which induces formation of a complex with phospha-tidylinositol-3-OH kinase, mediated by the SH2 domains of the p85 subunit of the kinase. Phosphatidylinositol-3-OH kinase is a heterodimer of this 85K regulatory subunit and a 11 OK catalytic subunit, and is a common substrate for most receptor tyrosine kinases and some cytokine receptors4,5, binding through its SH2 domain to phosphotyrosine in the motif Tyr-X-X-Met in the CD28 sequence, which is highly conserved between human, mouse and rat6–8 and lies in the intracellular domain. We show that CD28 mutants that have their kinase-binding site deleted or the tyrosine at position 173 substituted by phenylalanine do not associate with the kinase after CD28 stimulation and cannot stimulate production of interleukin-2. Our results suggest that phosphatidylinositol-3-OH kinase is critical for signalling by CD28. More... »

PAGES

327-329

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/369327a0

DOI

http://dx.doi.org/10.1038/369327a0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1014137295

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/8183372


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