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. Author manuscript; available in PMC: 2013 Sep 4.
Published in final edited form as: Sci Transl Med. 2012 Dec 12;4(164):164ra159. doi: 10.1126/scitranslmed.3004566

Fig. 7.

Fig. 7

Loss of RORγt, but not IL-17, restores Treg anti-inflammatory function. (A) Frequency of MC progenitors (MCp) among total mononuclear cells (MNCs) isolated from the intestine of Rag−/− mice and cultured without (n = 5) or with Tregs at 1:1 ratio from wild-type B6 (n = 6), APCΔ468 (n = 5), or IL-17−/− BM in APCΔ468 (n = 6), or with RORγt−/−xAPCΔ468 (n = 5) mice. (B) Compiled values of percent MC degranulation sensitized (IgE) and cross-linked with anti-IgE (IgE + Ag) and incubated without (n = 10) or with Tregs from wild-type B6 (n = 16), APCΔ468 (n = 15), IL-17−/− BM in APCΔ468 (n = 8), or RORγt−/−xAPCΔ468 (n = 10) mice. (C) Frequency of polyps after retro-orbital adoptive transfer of 5 × 105 Tregs into 2.5-month-old APCΔ468 mice. Polyp number was determined 3 weeks later. B6 (n = 5), APCΔ468 (n = 4), RORγt−/−xAPCΔ468 (n = 3). (D) Representative dot plot of intracellular cytokines in Tregs derived from the spleen of wild-type B6 or RORγt−/− mice. Purified Tregs were cultured without or with MCs for 5 days in the presence of IL-2 and stem cell factor (SCF). Cells were gated on live CD4+CD25+Foxp3+ cells (n = 3). Statistics are found in table S7.