The CD4/CD8:p56lck complex in T lymphocytes: a potential mechanism to regulate T-cell growth

Abstract

The CD4 and CD8 antigens on the surface of T cells appear to bind to major histocompatibility complex (MHC) class II and I antigens, respectively. These receptors have also been found to regulate T cell growth in a manner independent of MHC recognition. In this report, we describe recent work showing that the CD4 and CD8 receptors are coupled to a protein-tyrosine kinase, p56^lck, from T lymphocytes. The p56^lck protein is a member of the src family, which plays a crucial role in the activation and transformation of various mammalian cells. The CD4/CD8:p56^ck complex is catalytically active as shown by its ability to phosphorylate at 55–60 kDa. Two-dimensional, nonequilibrium gel electrophoresis demonstrated the similarity of p56^lck associated with the CD4 and CD8 antigens. Detergents were found to vary in their ability to solubilize the CD4:p56^lck complex in a catalytically active form. We further demonstrated by in vitro phosphorylation that members of the CD3 complex including the γ, δ, and ε chains, as well as a putative ζ subunit can be phosphorylated at tyrosyl residues by the CD4/CD8:p56^lck complex. Thus, this interaction may play an important role in the activation of T cells, and may mediate the cooperative interaction between the CD4/CD8 antigens and the Ti(TcR)/CD3 complex. This interaction also represents a possible precedent by which other members of the src family (c-src, c-yes, c-fgr, etc.) may be found to interact with mammalian growth receptors.Key words: CD4, CD8, protein-tyrosine kinase p56^lck.