Figure 4.
rhIGFBP7 and ATRA combination treatment does not affect healthy NBM cells. NBM cells derived from healthy donors were incubated with PBS (Ctrl), 100 µg/mL rhIGFBP7, 0.5 µM ATRA, or the combination (Combi) for 5 to 7 days. The effects of the treatments were normalized against untreated control cells and plotted as mean ± SEM. NBM samples were analyzed for the percentage of viable cells (A), CD45dim cells (B), myeloid CD45dimCD33+ cells (C), CD45dimCD34+ cells (D), CD3+ T cells (E), and CD19+ B cells (F) using flow cytometry and quantified relative to flow count beads. (G) CFU progenitor assays of NBM samples (in duplicate) after 7 days of treatment.

rhIGFBP7 and ATRA combination treatment does not affect healthy NBM cells. NBM cells derived from healthy donors were incubated with PBS (Ctrl), 100 µg/mL rhIGFBP7, 0.5 µM ATRA, or the combination (Combi) for 5 to 7 days. The effects of the treatments were normalized against untreated control cells and plotted as mean ± SEM. NBM samples were analyzed for the percentage of viable cells (A), CD45dim cells (B), myeloid CD45dimCD33+ cells (C), CD45dimCD34+ cells (D), CD3+ T cells (E), and CD19+ B cells (F) using flow cytometry and quantified relative to flow count beads. (G) CFU progenitor assays of NBM samples (in duplicate) after 7 days of treatment.

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