Figure 3.
Figure 3. Alterations in the peripheral T cell compartment in CD11cΔMHCII mice. WT and CD11cΔMHCII mice were assessed by flow cytometry for the T cell compartment at 12 weeks (n = 11, 13), 20 weeks (n = 22, 16), 30 weeks (n = 18, 11), and 1 year (n = 22, 25) of age. (A) Percentages of T cell subsets in the thymus at 30 weeks (n = 6, 7). (B) Percentages of total CD4+ T cells among total splenocytes. (C) Percentages of naive CD4+ T cells (CD4+CD62L+CD44−) among CD4+ T splenocytes. (D) Percentages of Treg cells (CD4+Foxp3+) gated on splenic CD4+ T cells. (E) Percentages of CD8+ T cells among total splenocytes. (F) Percentages of effector CD8+ T cells (CD8+CD62L−CD44+) gated on splenic CD8+ T cells. Median and individual data points are shown.

Alterations in the peripheral T cell compartment in CD11cΔMHCIImice. WT and CD11cΔMHCII mice were assessed by flow cytometry for the T cell compartment at 12 weeks (n = 11, 13), 20 weeks (n = 22, 16), 30 weeks (n = 18, 11), and 1 year (n = 22, 25) of age. (A) Percentages of T cell subsets in the thymus at 30 weeks (n = 6, 7). (B) Percentages of total CD4+ T cells among total splenocytes. (C) Percentages of naive CD4+ T cells (CD4+CD62L+CD44) among CD4+ T splenocytes. (D) Percentages of Treg cells (CD4+Foxp3+) gated on splenic CD4+ T cells. (E) Percentages of CD8+ T cells among total splenocytes. (F) Percentages of effector CD8+ T cells (CD8+CD62LCD44+) gated on splenic CD8+ T cells. Median and individual data points are shown.

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