Figure 2.
Figure 2. The signaling cascade mediated by Dd-ζ is intact in transfected Jurkat cells. (A) Flow cytometric analysis of Dd and Dd-ζ expression in transfected Jurkat cells. Open histograms represent isotype matched, fluorochrome-labeled control Ab. Closed histograms show staining with anti-CD3 (top panels) or anti-Dd (bottom panels). (B) Dd-ζ–transfected EL4 cells are killed by Dd-specific CTLs. EL4 cells that were untransfected (▪) or transfected with either the MHC-Dd (▴)or Dd-ζ (♦) constructs were used as targets for Dd-specific CTLs in a 51Cr release cytotoxicity assay. • indicates P815 cells. (C) IL-2 production by Dd-ζ–transfected Jurkat cells following cross-linking with anti-Dd mAb. Following incubation with anti-Dd (34-2-12) or anti-CD3 (OKT3) mAbs, the cells were treated with PMA and cross-linked with plate-bound anti-IgG. Supernatant fluid was tested in a proliferation assay for IL-2 content measuring 3H-thymidine uptake by CTLL-2 cells.

The signaling cascade mediated by Dd-ζ is intact in transfected Jurkat cells. (A) Flow cytometric analysis of Dd and Dd-ζ expression in transfected Jurkat cells. Open histograms represent isotype matched, fluorochrome-labeled control Ab. Closed histograms show staining with anti-CD3 (top panels) or anti-Dd (bottom panels). (B) Dd-ζ–transfected EL4 cells are killed by Dd-specific CTLs. EL4 cells that were untransfected (▪) or transfected with either the MHC-Dd (▴)or Dd-ζ (♦) constructs were used as targets for Dd-specific CTLs in a 51Cr release cytotoxicity assay. • indicates P815 cells. (C) IL-2 production by Dd-ζ–transfected Jurkat cells following cross-linking with anti-Dd mAb. Following incubation with anti-Dd (34-2-12) or anti-CD3 (OKT3) mAbs, the cells were treated with PMA and cross-linked with plate-bound anti-IgG. Supernatant fluid was tested in a proliferation assay for IL-2 content measuring 3H-thymidine uptake by CTLL-2 cells.

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