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-α, TCR-β, CD3-δ, CD3-ε and TCR-ζ chains, but lacked CD3-γ. 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-γ.
CITATION STYLE
Pérez-Aciego, P., Alarcón, B., Arnaiz-Villena, A., Terhorst, C., Timón, M., Segurado, O. G., & Regueiro, J. R. (1991). Expression and function of a variant T Cell receptor complex lacking CD3-γ. Journal of Experimental Medicine, 174(2), 319–326. https://doi.org/10.1084/jem.174.2.319
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