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. 2019 Jan 24;9:658. doi: 10.1038/s41598-018-37074-9

Figure 5.

Figure 5

(A) Shown are the number of splenic CD4+ T cells, CD8+ T cells, CD11b+ cells and B220+ B cells 14 days after BMT enumerated via FACS analysis. Values are the mean ± SEM of 3–5 mice per group (*p < 0.05). (B) Representative results demonstrate the frequency of splenic CD25+ FoxP3+ T cells in allogeneic BMT mice within indicated gates among total CD4+ spleen live cells. The percentages of splenic CD25+FoxP3+ T cells within splenic CD4+ cells 14 days after BMT are also shown (n = 4–5 mice per group; *p < 0.05). (C) Representative results demonstrate the frequency of skin CD25+ FoxP3+ T cells in allogeneic BMT mice within indicated gates among total CD4+ skin live cells. The percentages of skin CD25+FoxP3+ T cells within skin CD4+ cells 14 days after BMT are also shown (n = 4–5 mice per group; **p < 0.01). (D) Representative results demonstrate the frequency of splenic CD25+ FoxP3+ T cells in BALB/C mice within indicated gates among total CD4+ spleen live cells. The percentages of splenic CD25+FoxP3+ T cells within splenic CD4+ cells at day 14 are also shown (n = 4–5 mice per group; **p < 0.01). All data are representative of two independent experiments.