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. 2010 Mar 8;107(12):5540–5544. doi: 10.1073/pnas.0912675107

Fig. 5.

Fig. 5.

CD4 T cells from ApcMin/+ mice are functionally altered. (A) CD4 T cells from ApcMin/+ mice were isolated and activated with given amount of anti-CD3 and T cell–depleted irradiated splenocytes for 72 h. (B) Foxp3+ regulatory T cells were isolated from ApcMin/+ Foxp3-IRES-RFP mice and cocultured with Foxp3- CD4 effector T cells from either ApcMin/+ mice or their littermate control for 72 h for given ratios. (C) CD4 T cells from ApcMin/+ mice were isolated and activated for 96 h, and cytokines were measured by cytokine bead array. Data indicate means ± SD of three separate experiments as triplicates.