Figure 5
Figure 5. Early CD8α+ DC expansion after transplantation depends on Irf8 and Nfil3 but not Id2. (A) Analysis of CD11c+CD45RA− DCs from spleens of bone marrow chimeric mice in which Id2gfp/gfp, Id2fl/flCD11cCreT/+, Id2gfp/gfpNfil3−/−, or Id2gfp/gfpIrf8−/−-deficient bone marrow was transplanted into lethally irradiated recipients (Ly5.1+) 15 to 20 days earlier. Cells were stained for various surface molecules and analyzed by flow cytometry. Data are representative of 2 to 3 separate experiments with 2 to 4 mice in each experiment with similar results (n = 6-8 mice per group). (B) Analysis of CD8α expression on DCs in the absence of Nfil3 or Id2. DCs were isolated from spleens of intact Id2gfpNfil3−/− or Id2CD11cCreT/+ mice. Data are representative of 2 experiments with similar results (n = 5 mice per genotype). (C) Proportion (top panel) and total number (bottom panel) of splenic CD8α+ DCs recovered from spleens of intact WT and KO mice or bone marrow chimeric (KO→Ly5.1) mice 3 weeks after transplantation. Data are pooled from 2 experiments with 5 mice per genotype; NS indicates not statistically significant.

Early CD8α+ DC expansion after transplantation depends on Irf8 and Nfil3 but not Id2. (A) Analysis of CD11c+CD45RA DCs from spleens of bone marrow chimeric mice in which Id2gfp/gfp, Id2fl/flCD11cCreT/+, Id2gfp/gfpNfil3−/−, or Id2gfp/gfpIrf8−/−-deficient bone marrow was transplanted into lethally irradiated recipients (Ly5.1+) 15 to 20 days earlier. Cells were stained for various surface molecules and analyzed by flow cytometry. Data are representative of 2 to 3 separate experiments with 2 to 4 mice in each experiment with similar results (n = 6-8 mice per group). (B) Analysis of CD8α expression on DCs in the absence of Nfil3 or Id2. DCs were isolated from spleens of intact Id2gfpNfil3−/− or Id2CD11cCreT/+ mice. Data are representative of 2 experiments with similar results (n = 5 mice per genotype). (C) Proportion (top panel) and total number (bottom panel) of splenic CD8α+ DCs recovered from spleens of intact WT and KO mice or bone marrow chimeric (KO→Ly5.1) mice 3 weeks after transplantation. Data are pooled from 2 experiments with 5 mice per genotype; NS indicates not statistically significant.

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