Figure 3
Figure 3. Ablation of A20 in the B-lineage has B cell-extrinsic effects on immune homeostasis. (A) Dot-plots showing percentages of CD4+Foxp3+ regulatory T cells and CD4+CD25− T cells (naïve indicates CD44intCD62Lhi; memory, CD44hiCD62Lhi; and effector, CD44hiCD62Llo) in the spleen. Numbers indicate the mean of 4 to 6 mice for each genotype. (B-D) Absolute cell numbers of CD4 T (B), CD8 T (C), and myeloid cell (D) subsets in BA20−/−, BA20+/−, and CD19cre mice (n = 6 per group; 8-12 weeks old). Data are mean ± SD. Treg indicates Foxp3+; naive, CD44intCD62Lhi; memory, CD44hiCD62Lhi; effector/memory, CD44hiCD62Llo; DC, dendritic cell (CD11c+); Eos, eosinophils (Gr1intSiglecF+); Mac, macrophages (Mac1+Gr1lo); and Neu, neutrophils (Gr1hiLy6G+). (E) Intracellular cytokine staining of ex vivo isolated splenocytes (gated on T cells). Numbers represent mean plus or minus SD of 3 mice per genotype. *P < .05 (1-way analysis of variance). **P < .001 (1-way analysis of variance).

Ablation of A20 in the B-lineage has B cell-extrinsic effects on immune homeostasis. (A) Dot-plots showing percentages of CD4+Foxp3+ regulatory T cells and CD4+CD25 T cells (naïve indicates CD44intCD62Lhi; memory, CD44hiCD62Lhi; and effector, CD44hiCD62Llo) in the spleen. Numbers indicate the mean of 4 to 6 mice for each genotype. (B-D) Absolute cell numbers of CD4 T (B), CD8 T (C), and myeloid cell (D) subsets in BA20−/−, BA20+/−, and CD19cre mice (n = 6 per group; 8-12 weeks old). Data are mean ± SD. Treg indicates Foxp3+; naive, CD44intCD62Lhi; memory, CD44hiCD62Lhi; effector/memory, CD44hiCD62Llo; DC, dendritic cell (CD11c+); Eos, eosinophils (Gr1intSiglecF+); Mac, macrophages (Mac1+Gr1lo); and Neu, neutrophils (Gr1hiLy6G+). (E) Intracellular cytokine staining of ex vivo isolated splenocytes (gated on T cells). Numbers represent mean plus or minus SD of 3 mice per genotype. *P < .05 (1-way analysis of variance). **P < .001 (1-way analysis of variance).

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