Figure 4
Figure 4. Foxp1-deficient Treg cells develop normally and are functional. (A) Staining of cell-surface CD4 and CD25 and intracellular Foxp3 in the thymuses, lymph nodes, and spleens of 10-week-old Foxp1f/+Cd4Cre and Foxp1f/fCd4Cre mice. The percentages of CD25+Foxp3+ cells in CD4+ T cells were shown. Data are representative of 2 independent experiments. (B) Total cell numbers of Treg cells in the thymuses, lymph nodes, and spleens of Foxp1f/+Cd4Cre and Foxp1f/fCd4Cre mice at different ages. Bars represent average ± SD, weeks 4-5: n = 5, weeks 8-10: n = 7, and weeks 21-22: n = 5. (C) In Treg cell suppression cocultures, CFSE-labeled control CD4+ T cells were incubated with various ratios of Treg cells from Foxp1f/+Cd4Cre or Foxp1f/fCd4Cre mice. The IFN-γ production by control CD4+ T cells was analyzed by intracellular staining. Data are representative of 2 independent experiments.

Foxp1-deficient Treg cells develop normally and are functional. (A) Staining of cell-surface CD4 and CD25 and intracellular Foxp3 in the thymuses, lymph nodes, and spleens of 10-week-old Foxp1f/+Cd4Cre and Foxp1f/fCd4Cre mice. The percentages of CD25+Foxp3+ cells in CD4+ T cells were shown. Data are representative of 2 independent experiments. (B) Total cell numbers of Treg cells in the thymuses, lymph nodes, and spleens of Foxp1f/+Cd4Cre and Foxp1f/fCd4Cre mice at different ages. Bars represent average ± SD, weeks 4-5: n = 5, weeks 8-10: n = 7, and weeks 21-22: n = 5. (C) In Treg cell suppression cocultures, CFSE-labeled control CD4+ T cells were incubated with various ratios of Treg cells from Foxp1f/+Cd4Cre or Foxp1f/fCd4Cre mice. The IFN-γ production by control CD4+ T cells was analyzed by intracellular staining. Data are representative of 2 independent experiments.

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