Binding of phosphatidyl-inositol-3-OH kinase to CD28 is required for T-cell signalling
Hybridomas
Recombinant Fusion Proteins
T-Lymphocytes
Immunoblotting
Transfection
Precipitin Tests
Mice
Phosphatidylinositol 3-Kinases
Phosphotransferases (Alcohol Group Acceptor)
03 medical and health sciences
L Cells
0302 clinical medicine
CD28 Antigens
Mutation
Animals
Humans
Phosphorylation
Protein Binding
Signal Transduction
DOI:
10.1038/369327a0
Publication Date:
2003-06-12T23:53:12Z
AUTHORS (7)
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 complex. 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 concentrations. These differences suggest that each pathway provides unique biochemical information 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 phosphatidylinositol-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 110K catalytic subunit, and is a common substrate for most receptor tyrosine kinases and some cytokine receptors, 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 rat 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.
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