Figure 2
Figure 2. Notch signaling is important for human CD8+ T cell priming. Primary naive CD8+ T cells were cocultured with autologous Mart-1 peptide–loaded moDCs (3 µg/mL peptide), both isolated from an HLA-A2–typed healthy donor, as described in the Methods. Inhibition of Notch during CD8+ T-cell priming, either via (A) GSI (10 μM) or (B) soluble DLL4-Fc (5 μg/mL) resulted in diminished expansion of Mart-1–specific CD8+ T cells, as reflected by A2/Mart-1-tetramer staining using flow cytometry. The results shown are from 2 different donors. Similar results were obtained in 5 independent experiments.

Notch signaling is important for human CD8+ T cell priming. Primary naive CD8+ T cells were cocultured with autologous Mart-1 peptide–loaded moDCs (3 µg/mL peptide), both isolated from an HLA-A2–typed healthy donor, as described in the Methods. Inhibition of Notch during CD8+ T-cell priming, either via (A) GSI (10 μM) or (B) soluble DLL4-Fc (5 μg/mL) resulted in diminished expansion of Mart-1–specific CD8+ T cells, as reflected by A2/Mart-1-tetramer staining using flow cytometry. The results shown are from 2 different donors. Similar results were obtained in 5 independent experiments.

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