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. 2014 Sep 30;111(41):14858–14863. doi: 10.1073/pnas.1404264111

Fig. 1.

Fig. 1.

The absence of Tsc1 diminishes the generation of memory T cells. (A) Flow cytometry of the frequency of Kb-OVA+ CD8+ T cells in the blood from WT and Tsc1−/− mice infected with LM–OVA at the indicated time points (*P < 0.05, **P < 0.01). (B) Number of Kb-OVA+ CD8+ T cells in the spleen from WT and Tsc1−/− mice at days 0, 9, 18, and 41 p.i. (C) Flow cytometry of CD8+ T cells (Left) and the number of Kb-OVA+ CD8+ T cells (Right) in the spleen and liver from WT and Tsc1−/− mice at day 41 p.i. (D) Splenocytes from WT and Tsc1−/− mice at day 41 p.i. were restimulated with the SIINFEKL peptide for intracellular cytokine staining of IFN-γ and TNF-α. Shown are representative flow cytometry plots of CD8+ T cells (Left) and the number (Right) of IFN-γ+ and TNF-α+ CD8+ T cells. Data are representative of three independent experiments and are presented as the mean ± SEM.