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. Author manuscript; available in PMC: 2018 Dec 13.
Published in final edited form as: Nature. 2018 May 30;558(7708):141–145. doi: 10.1038/s41586-018-0177-0

Figure 2. Mst1/2 are selectively required in CD8α+ DCs to orchestrate CD8+ T-cell homeostasis and function.

Figure 2.

a, b, Frequencies of CD44highCD62Llow (a) and CD44+IFN-γ+ cells (b) in splenic T cells from WT (n = 5), Mst1/2ΔDC (n = 3), Batf3−/− (n = 4) and Mst1/2ΔDCBatf3−/− (n = 4) mice. c, CFSE dilution of donor OT-I T cells in WT, Mst1/2ΔDC, Batf3−/−:WT or Batf3−/−:Mst1/2ΔDC mixed chimeras immunized with OVA. d, Frequency and number of IFN-γ+ cells among H-2Kb-OVA+ CD8+ T cells after immunization with OVA-loaded irradiated B2m−/− splenocytes (n = 4 per genotype). e, Thymidine incorporation of OT-I T cells cultured with OVA protein- or OVA(257-264) peptide-pulsed CD8α+ or CD8α DCs (n = 8 per genotype). f, IL-2 from co-cultures in e (n = 6 per genotype for CD8α+ DCs, and n = 8 per genotype for CD8α DCs). Error bar indicates SEM. NS, not significant; *P < 0.05; **P < 0.01; one-way ANOVA in a, b; two-tailed unpaired Student’s t-test in df. Data summarize two (f, c), three (d, e) or four (a, b) independent experiments.