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. 2013 Jan 2;123(2):580–593. doi: 10.1172/JCI65013

Figure 8. Suppressive function of Cd28-ΔTregs.

Figure 8

(A) In vitro suppression assay. Sorted WT naive cells were stimulated by soluble CD3 and T cell–depleted splenocytes with the addition of different ratios of WT Tregs or Cd28-ΔTregs. Tregs were sorted from 4-week-old mice. Teff, effector T cells. (B) In vivo colitis induction. Weight loss of Rag1–/– mice adoptively transferred with sorted CD4+CD45RBhi effector T cells with or without WT Tregs or Cd28-ΔTregs. A total of 6 mice were analyzed for each group. Data represent mean ± SEM. (C) H&E staining of the colons of mice in B. Original magnification, ×100. (D and E) Representative analysis of donor CD45.1+CD4+ effector cells and regulatory cells in the colons of mice in B. (F) Sorted WT Tregs or Cd28-ΔTregs were labeled with CellTrace Violet and adoptively transferred to Rag1–/– hosts. Lymph node cells were analyzed 7 days after transfer. Data are representative of 3 experiments.