CD28 OF T-LYMPHOCYTES ASSOCIATES WITH PHOSPHATIDYLINOSITOL 3-KINASE

T lymphocyte activation requires recognition of antigen by the antigen specific TCR as well as second co-stimulatory signals. This recogniti on event results in the activation of non-TCR linked protein tyrosine kinases (PTKs). The mechanism of co-stimulation of T cells is unknown except for the involvement of PTKs. The T cell surface molecule CD28 i s effective in delivering co-stimulatory signals and prevents T cell a nergy by inducing T cell proliferation in TCR stimulated T cells, prim arily due to an increase in IL-2 production. The mechanism by which CD 28 mediates this effect is currently unknown. Some conventional recept or molecules possess intrinsic tyrosine kinase and as a consequence of cross-linking or ligand binding, phosphorylate numerous tyrosines wit hin their cytoplasmic tall, leading these tyrosines to become 'activat ed' and bind cytoplasmic effector molecules possessing Src homology 2 domains which specifically recognize phosphorylated tyrosines. One suc h cytoplasmic effector molecule is the phosphatidylinositol-3-phosphat e kinase (PI3 kinase) which recognizes the motif phosphotyrosine - met hione/valine - X - methionine (X being any amino acid) within the cyto plasmic tails of numerous receptor tyrosine kinases. As CD28 contains a copy of the Pl3 kinase binding motif within its cytoplasmic tall, we investigated CD28 signaling and Pl3 kinase activation. Here we demons trate using the Jurkat cell line that CD28 becomes tyrosine phosphoryl ated following CD28 cross-linking and associates with Pl3 kinase. Furt hermore, a synthetic peptide representing the YM/VXM motif within the cytoplasmic tail of CD28 also interacts with Pl3 kinase only when the tyrosine is phosphorylated. CD28 co-stimulation, therefore, similar to that of CD19 and 'co-stimulation' of B cells travel in part via the a ctivation of the Pl3 kinase pathway.