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. Author manuscript; available in PMC: 2018 Aug 24.
Published in final edited form as: J Immunol. 2006 Nov 1;177(9):5852–5860. doi: 10.4049/jimmunol.177.9.5852

Figure 5. Accumulation of the IL-10-producing progeny of CD4+CD25+ T cells within the colon.

Figure 5

Rag-1−/− mice were injected with 4 × 105 wild-type CD45.2+CD4+CD45RBhigh T cells. After development of colitis, mice received a second transfer of 1 × 106 congenic CD45.1+ CD4+CD25+ T cells. After 4 wk, the ability of CD4+CD45RBhigh (n = 6) and CD4+CD25+ (n = 6) progeny to produce IL-10 and IFN-γ was analysed. Lymphocytes were prepared from spleen, MLN, and the colonic LP and stimulated with PMA/ionomycin and brefeldin A. The results of two independent experiments are pooled. (a) Representative FACS plot showing preferential IL-10 production by LP CD4+CD25+ T cell progeny (CD45.1+) and preferential IFN-γ production by the CD4+CD45RBhigh T cell progeny (CD45.1). (b) Production of IL-10 and IFN-γ by CD4+CD25+ T cell progeny and comparison of IL-10 and IFN-γ production by CD4+CD45RBhigh T cell progeny in the presence or absence of CD4+CD25+ T cells. Data are shown for spleen, MLN, and LP. Significance was tested using the Mann-Whitney U test; n.s., not significant.