Figure 1
Figure 1. IKDCs differ from otherwise similar Ly6C+ pDCs with respect to RAG-1 and patterns of gene expression. (A) The B220+RAG-1/GFP+ population freshly isolated from BM did not include IKDCs. (B) Conversely, BM IKDCs do not express RAG-1 detectable in RAG-1/GFP reporter mice or by RT-PCR. (C) Transcripts for a series of genes were measured in highly purified cells by RT-PCR. (D) Wild-type mice were compared with Id2 gene–targeted animals (Id2−/−) by flow cytometry. Mean ± SEM values are shown for NK1.1+ CD11c− NK cells, B220+CD11c+CD19−Ly-6C− NK1.1+ IKDCs, and B220+CD11c+CD19−Ly-6C+NK1.1− pDCs in BM. (E) Rigorously sorted DC subsets were placed in overnight cultures with CpG ODN, and supernatants were tested for the 3 indicated cytokines. The results are representative of 3 independent experiments.

IKDCs differ from otherwise similar Ly6C+ pDCs with respect to RAG-1 and patterns of gene expression. (A) The B220+RAG-1/GFP+ population freshly isolated from BM did not include IKDCs. (B) Conversely, BM IKDCs do not express RAG-1 detectable in RAG-1/GFP reporter mice or by RT-PCR. (C) Transcripts for a series of genes were measured in highly purified cells by RT-PCR. (D) Wild-type mice were compared with Id2 gene–targeted animals (Id2−/−) by flow cytometry. Mean ± SEM values are shown for NK1.1+ CD11c NK cells, B220+CD11c+CD19Ly-6C NK1.1+ IKDCs, and B220+CD11c+CD19Ly-6C+NK1.1 pDCs in BM. (E) Rigorously sorted DC subsets were placed in overnight cultures with CpG ODN, and supernatants were tested for the 3 indicated cytokines. The results are representative of 3 independent experiments.

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