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. Author manuscript; available in PMC: 2013 Dec 26.
Published in final edited form as: J Immunol. 2010 Jun 14;185(2):10.4049/jimmunol.0903144. doi: 10.4049/jimmunol.0903144

Figure 5. Characteristics of CCR4/FoxP3 chimeras.

Figure 5

(A) Splenocytes were stained for FoxP3, CD4 and CD25 and analyzed via flow cytometry eleven weeks after BM reconstitution. Representative dot plots are shown. Numbers indicate the average percentage of FoxP3+ and CD4+ double positive splenocytes ± SEM (n = 3). The average percentages of FoxP3+ CD4+ of total CD4+ cells constituted 19.5% ± 2.2 for WT and 32.5% ± 0.1 for CCR4/FoxP3 chimeras. (B) Serum IgE levels in WT, FoxP3KO mice and CCR4/FoxP3 and CCR4/WT chimeras four weeks (hatched column, n = 31 per group) and eleven weeks (black column, n = 3 per group) after BM reconstitution. (C) IL-4 mRNA measured by quantitative real-time PCR in skin of WT, FoxP3KO, CCR4/FoxP3 and CCR4/WT chimeras four weeks (hatched column, n = 12 per group) and eleven weeks (black column, n = 6 per group) after BM reconstitution. Relative expression of IL-4 is represented in relation to GAPDH. *p < 0.05, ***p < 0.0001