Figure 2
Figure 2. Suppressive function of CD200R3 expressed on DCs in the Ag-specific CD4+ T-cell response. (A) The expression of cell surface molecules on retroviral transfected BM-iDCs was analyzed by flow cytometry, and data are represented by a dot plot. Data are representative of 4 replicate experiments. (B) Rag2−/−KJ1-26+ T cells (5 × 104) were cultured with OVAp/CD200R3−GFP−BM-iDCs, OVAp/CD200R3−GFP+BM-iDCs, or OVAp/CD200R3+GFP+BM-iDCs (6.25 × 102-5 × 103) for 3 days, and the proliferative response was measured. * P < .01 compared with OVAp/CD200R3−GFP−BM-iDCs. Data are mean ± SEM, and the results are combined from 4 replicate experiments.

Suppressive function of CD200R3 expressed on DCs in the Ag-specific CD4+ T-cell response. (A) The expression of cell surface molecules on retroviral transfected BM-iDCs was analyzed by flow cytometry, and data are represented by a dot plot. Data are representative of 4 replicate experiments. (B) Rag2−/−KJ1-26+ T cells (5 × 104) were cultured with OVAp/CD200R3GFPBM-iDCs, OVAp/CD200R3GFP+BM-iDCs, or OVAp/CD200R3+GFP+BM-iDCs (6.25 × 102-5 × 103) for 3 days, and the proliferative response was measured. * P < .01 compared with OVAp/CD200R3GFPBM-iDCs. Data are mean ± SEM, and the results are combined from 4 replicate experiments.

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