Figure 6
Figure 6. Blimp1 expression in NK cells is independent of IRF4 and Bcl6. (A) DX5+ NK cells were expanded in IL-15 for 5 days and then transferred into cytokines for 2 days as indicated. Protein extracts were subjected to Western blotting with antibodies to the indicated proteins. (B) Blimp1gfp/+ mice were bred on Irf4−/− or Bcl6−/− backgrounds and TCRβ−NK1.1+CD49b+ NK cells were analyzed for Blimp1/GFP expression (empty histogram, wild-type control; filled black histogram, Blimp1gfp/+; filled gray histogram, Blimp1gfp/+ and deficient for the indicated transcription factor). (C) Flow cytometric analysis of splenocytes isolated from Irf4−/−, Bcl6−/−, or control mice (top panel). Gated TCRβ−NK1.1+CD49b+ NK cells are shown in the lower panel. Numbers indicate the proportion of cells of the indicated phenotype. The results shown are representative of 3-6 independent experiments.

Blimp1 expression in NK cells is independent of IRF4 and Bcl6. (A) DX5+ NK cells were expanded in IL-15 for 5 days and then transferred into cytokines for 2 days as indicated. Protein extracts were subjected to Western blotting with antibodies to the indicated proteins. (B) Blimp1gfp/+ mice were bred on Irf4−/− or Bcl6−/− backgrounds and TCRβNK1.1+CD49b+ NK cells were analyzed for Blimp1/GFP expression (empty histogram, wild-type control; filled black histogram, Blimp1gfp/+; filled gray histogram, Blimp1gfp/+ and deficient for the indicated transcription factor). (C) Flow cytometric analysis of splenocytes isolated from Irf4−/−, Bcl6−/−, or control mice (top panel). Gated TCRβNK1.1+CD49b+ NK cells are shown in the lower panel. Numbers indicate the proportion of cells of the indicated phenotype. The results shown are representative of 3-6 independent experiments.

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