Figure 4
Figure 4. RAG1 expression in CMP and CMP-derived pDCs. CMPs were isolated from the BM of RAG1-GFP reporter mice and analyzed by for expression of flt3 and RAG1 (A), Flt3+ RAG1+ (B), or flt3+RAG1+ and flt3+RAG1− CMP were sorted from the BM of RAG1-GFP reporter mice and cultured with GM-CSF (B; 10 ng/mL) or FL (C). (B) Progeny were analyzed after 7 days and macrophages identified as CD11bhighF4/80+. (C) After 5 days, pDCs were identified as CD11c+ BST-2+ and cDCs identified as CD11c+BST-2−. The GFP expression of RAG1+ CMP-derived cDCs (light gray shaded histogram) and pDCs (dark gray shaded histogram) and RAG1− CMP-derived cDCs (dashed line) and pDCs (solid line) was analyzed by flow cytometry. Plots are representative of 5 (A), 2 (B), or 4 (C) independent experiments.

RAG1 expression in CMP and CMP-derived pDCs. CMPs were isolated from the BM of RAG1-GFP reporter mice and analyzed by for expression of flt3 and RAG1 (A), Flt3+ RAG1+ (B), or flt3+RAG1+ and flt3+RAG1 CMP were sorted from the BM of RAG1-GFP reporter mice and cultured with GM-CSF (B; 10 ng/mL) or FL (C). (B) Progeny were analyzed after 7 days and macrophages identified as CD11bhighF4/80+. (C) After 5 days, pDCs were identified as CD11c+ BST-2+ and cDCs identified as CD11c+BST-2. The GFP expression of RAG1+ CMP-derived cDCs (light gray shaded histogram) and pDCs (dark gray shaded histogram) and RAG1 CMP-derived cDCs (dashed line) and pDCs (solid line) was analyzed by flow cytometry. Plots are representative of 5 (A), 2 (B), or 4 (C) independent experiments.

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