The Journal of Experimental Medicine · 1991 · 69 citations · 21 references
Life SciencesCell BiologyImmunologyCell SignalingCellular ImmunologySignal TransductionAntigen RecognitionHuman Leukocyte Antigen SystemT Cell ActivationT Cell BiologyT Cell DevelopmentT Cell Receptor SignalingAntigen Recognition DomainsCalcium Flux AnalysisCd3 Complex DefectsIndirect Immunofluorescence AssayT Cell Epitope RecognitionT Cell Receptor StructureT Cell ReceptorsT-cell Epitopes
A T cell line termed DIL2 has been derived from an infant with a polyclonal T cell receptor (TCR)/CD3 cell surface expression defect. Indirect immunofluorescence showed that the expression of certain TCR/CD3 epitopes (like those detected by WT31 and BMA031 monoclonals) was strongly reduced (around five-fold) on DIL2, whereas other epitopes (like those detected by SP34 and Leu4) were only around two-fold lower than in normal T cell lines. Specific immunoprecipitates of surface-radioiodinated DIL2 cells contained TCR-alpha, TCR-beta, CD3-delta, CD3-epsilon and TCR-zeta chains, but lacked CD3-gamma. This structural TCR/CD3 variant was, however, capable of transducing certain activation signals, since normal proliferation and a low but significant calcium flux was observed in DIL2 cells after engagement with specific antibodies. Our data suggest that a functional TCR/CD3 complex can be expressed on the surface of T cells in the absence of CD3-gamma.
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T Cell Growth Factor: Parameters of Production and a Quantitative Microassay for Activity
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