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. 2020 Sep 28;218(1):e20181853. doi: 10.1084/jem.20181853

Figure S1.

Figure S1.

Lymphoid compartments appear unaltered in Nfatc1deltaSUMO mice in steady state. (A) Total cell number in thymus, spleen, and LNs of WT versus Nfatc1deltaSUMO mice (mean + SD, n > 3). (B) Determination of the number of B and T cells in spleen and LN of WT and Nfatc1deltaSUMO mice by surface staining to B220 and CD3ɛ and flow cytometry. (C and D) Distribution of CD4+ and CD8+ T cells (C) as well as frequency of CD25+ Foxp3+ T reg cells within the CD4+ T cell compartment (D) in thymus, spleen, and LNs of WT versus Nfatc1deltaSUMO mice analyzed by flow cytometry. (E) Detection of the activation status of CD4+ T cells in untreated WT versus Nfatc1deltaSUMO mice, given by representative flow cytometry for resting (CD62L+) and activated (CD69+) CD4+ T cells in spleen or LN. (F) Capacity of CD4+CD25+ T regs, isolated from WT and Nfatc1deltaSUMO mice, to suppress WT CD4+ T cells, stimulated on irradiated splenic cells with anti-CD3. The ratio of T conv over T regs are indicated. Bars show mean + SD of three experiments.