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. Author manuscript; available in PMC: 2019 May 23.
Published in final edited form as: Immunity. 2018 Dec 18;49(6):1049–1061.e6. doi: 10.1016/j.immuni.2018.10.008

Figure 1. Nlrc3 Is Down-regulated upon TCR Stimulation, Suppressing CD4+ T Cell Activation.

Figure 1

(A) Nlrc3 expression in splenic CD4+ T cells and CD8+ T cells from WT mice after activation by anti-CD3 (5 μg/mL) and anti-CD28 (2 μg/mL) antibodies.

(B) Nlrc3 expression in splenic CD4+ T cells from WT mice upon activation by anti-CD3 (5 μg/mL) and anti-CD28 (2 μg/mL) antibodies under Th0, Th1, and Th17 cell conditions.

(C) CD4+ T cells isolated from WT and Nlrc3−/− mice were stimulated with PMA (50 ng/mL) and ionomycin (1 μg/mL). Graphs show the percentage of CD4+CD25+ and CD4+CD69+ cells, MFI of CD25 among CD4+CD25+ cells, and MFI of CD69 among CD4+CD69+ cells after stimulation.

(D) Cells isolated from WT and Nlrc3−/− mice were stimulated with anti-CD3 (5 μg/mL) and anti-CD28 (2 μg/mL) antibodies. Graphs show the percentage of CD4+CD25+ and CD4+CD69+ cells, MFI of CD25 among CD4+CD25+ cells, and MFI of CD69 among CD4+CD69+ cells.

Data are from one experiment representative of two or three experiments and are shown as mean ± SEM of triplicate samples. Statistical significance was determined by unpaired t test. *p < 0.05, **p < 0.01, ***p < 0.001. See also Figures S1 and S2.