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. 2016 Jul 7;113(30):8490–8495. doi: 10.1073/pnas.1608873113

Fig. S1.

Fig. S1.

Schematic representation of reporter mice and lympho-proliferation of FoxP3-GFPcreKI/Y PD-1 KO mice. (A) Map of the FoxP3-GFPcre locus is shown. Filled boxes, exons; gray box, 3′UTR of Foxp3 gene; I, IRES. (B) Principle of Cre-Lox–mediated tdRFP. (C) The 3- to ∼11-wk-old male FoxP3-GFPcreKI/Y PD-1 WT or PD-1 KO mice were analyzed for serum lipase concentration (excluding the maximum and minimum values). (D) Total number of mononuclear cells in the pancreas, pancreatic LNs, SPL, and LNs of 3- to ∼10-wk-old FoxP3-GFPcreKI/Y PD-1 WT or PD-1 KO mice. (E) The number of CD4+ and CD8+ T cells from the pancreas and pancreatic LNs and the number of CD44+ in CD4+ or CD8+ T cells from the pancreatic LNs of mice are as in D. (F) The number of CD4+, CD8+, CD44+CD4+, CD44+CD8+, and FoxP3+(GFP+) T cells from the SPL of mice as in D. (G) LN cells were analyzed for the frequency and number of CD4+, CD8+, CD44+CD4+, CD44+CD8+, and FoxP3+ (GFP+) T cells and for the ratio of CD44+ (gated on CD4+ or CD8+ T cells) and FoxP3+ (GFP+) T cells of mice as in D. Data are representative of 3 to ∼7 mice per group and shown as the means (±SEM). *P < 0.05, **P < 0.01, ***P < 0.001.