Figure 6
Figure 6. DC-induced Foxp3+ T cells are suppressive in vitro. (A) Foxp3−CD25−CD4+ T cells from DO11.10 RAG−/− mice were cultured for 7 days with CD11c+ spleen DCs (2 × 104), peptide (0.03 μg/mL), and TGF-β (2 ng/mL). Cells were stained with anti-CD4, CD25, and Foxp3 Abs. (B) As in panel A, but live cells were stained with anti-CD4 and CD25 Abs for sorting. The square indicates the gate for sorting. (C) Sorted cells from (B) were fixed and further stained with anti-Foxp3 Ab. The purity of sorted natural CD25+CD4+ T regs was also shown. (D) CD25−CD4+ responder T cells (2 × 104) from DO11.10 mice were CFSE-labeled and stimulated with spleen APCs (105) and anti-CD3 mAb. To these, the induced Foxp3+ T regs purified as in panel C were added in graded numbers. After 3 days, CFSE dilution was analyzed with flow cytometry. Dead cells were gated out by TOPRO-3 iodide. Data are representative of 2 independent experiments.

DC-induced Foxp3+ T cells are suppressive in vitro. (A) Foxp3CD25CD4+ T cells from DO11.10 RAG−/− mice were cultured for 7 days with CD11c+ spleen DCs (2 × 104), peptide (0.03 μg/mL), and TGF-β (2 ng/mL). Cells were stained with anti-CD4, CD25, and Foxp3 Abs. (B) As in panel A, but live cells were stained with anti-CD4 and CD25 Abs for sorting. The square indicates the gate for sorting. (C) Sorted cells from (B) were fixed and further stained with anti-Foxp3 Ab. The purity of sorted natural CD25+CD4+ T regs was also shown. (D) CD25CD4+ responder T cells (2 × 104) from DO11.10 mice were CFSE-labeled and stimulated with spleen APCs (105) and anti-CD3 mAb. To these, the induced Foxp3+ T regs purified as in panel C were added in graded numbers. After 3 days, CFSE dilution was analyzed with flow cytometry. Dead cells were gated out by TOPRO-3 iodide. Data are representative of 2 independent experiments.

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