Figure 4
Figure 4. IKDCs develop efficiently from CD62L+ lymphocyte progenitors. (A) LSPs, ELPs, CMPs, and CLPs were sorted from Thy1.1 congenic RAG-1/GFP reporter mice, and 5 × 103 cells of each were transferred to sublethally irradiated recipients. Flow cytometry analyses were then performed 16 days after transplantation. Absolute numbers of donor-derived pDC (B220+ CD19−CD11c+ Ly6C+), IKDC (B220+ CD19−CD11c+ Ly6C− NK1.1+), and NK (NK1.1+ CD11c−) BM cells per femur are given (* denotes significant differences [P < .05]). (B) LSPs (103/well) were placed in OP9 cocultures with Flk-2/Flt-3 ligand and IL-15. They were subcultured to fresh stromal cell monolayers after one week, and gated B220+CD19−CD11c+ Ly6C− cells were assessed for NK1.1 expression by flow cytometry at the indicated intervals.

IKDCs develop efficiently from CD62L+ lymphocyte progenitors. (A) LSPs, ELPs, CMPs, and CLPs were sorted from Thy1.1 congenic RAG-1/GFP reporter mice, and 5 × 103 cells of each were transferred to sublethally irradiated recipients. Flow cytometry analyses were then performed 16 days after transplantation. Absolute numbers of donor-derived pDC (B220+ CD19CD11c+ Ly6C+), IKDC (B220+ CD19CD11c+ Ly6C NK1.1+), and NK (NK1.1+ CD11c) BM cells per femur are given (* denotes significant differences [P < .05]). (B) LSPs (103/well) were placed in OP9 cocultures with Flk-2/Flt-3 ligand and IL-15. They were subcultured to fresh stromal cell monolayers after one week, and gated B220+CD19CD11c+ Ly6C cells were assessed for NK1.1 expression by flow cytometry at the indicated intervals.

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