CD4-INDEPENDENT SIGNAL-TRANSDUCTION THROUGH THE T-CELL RECEPTOR (TCR/CD3)

The membrane-bound CD4 glycoprotein has been proposed to act like a co-receptor along with the T-cell antigen receptor (TCR/CD3) during ligand recognition and cell activation. Due to its association with the protein tyrosine kinase (PTK) p56(lck), CD4 is believed to transduce a signal and support CD3 activation of T cells. In this study we have shown that CD3 ligation on murine T-cell hybridomas induces tyrosine phosphorylation of proteins, including phospholipase C-yl (PLC gamma 1), both in the presence as well as in the absence of CD4-linked p56(lck). Furthermore, using HPB clones deficient in CD3/PTK association, it has been found that the presence of CD4/p56(lck) does not overcome the defect in signalling. Not even co-aggregation of CD4 with CD3 triggers tyrosine phosphorylation of proteins in these cells. Together, the present results indicate that CD3-linked PTK(s) plays a primary role in the induction of signalling through TCR/CD3, and the presence of CD4/p56(lck) is neither necessary nor sufficient to elicit these events. In the light of these results a possible role for CD4 in antigen presentation has been proposed.