Fig. 2.
Fig. 2. 0.8% to 1.7% of Lin−/34+/DRdim cells are myeloid-lymphoid initiating cells. Progeny from single Lin−/34+/DRdim cells cultured on AFT024 in expansion medium with Flt3-L, SCF, and IL-7 were replated after 4 weeks in 8 secondary plates. Four secondary plates were maintained in expansion medium with Flt3-L, SCF, and IL-7 to enumerate LTC-IC. The remaining 4 secondary plates were maintained in lymphoid differentiation medium to detect NK-IC. Lin−/34+/DRdim cells that generated ≥1 LTC-IC (black circles) and ≥1 NK-IC (gray circles) were identified as ML-IC.

0.8% to 1.7% of Lin/34+/DRdim cells are myeloid-lymphoid initiating cells. Progeny from single Lin/34+/DRdim cells cultured on AFT024 in expansion medium with Flt3-L, SCF, and IL-7 were replated after 4 weeks in 8 secondary plates. Four secondary plates were maintained in expansion medium with Flt3-L, SCF, and IL-7 to enumerate LTC-IC. The remaining 4 secondary plates were maintained in lymphoid differentiation medium to detect NK-IC. Lin/34+/DRdim cells that generated ≥1 LTC-IC (black circles) and ≥1 NK-IC (gray circles) were identified as ML-IC.

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