Figure 5
Figure 5. MLL-induced leukemia initiation/progression is independent of HIF-1α status, although MLL signals directly toward HIF. (A) GFP expression of a clone derived from doxycycline-inducible MLL-ENL BM cells transduced with a GFP-hypoxic reporter. Cells from this clone were grown in methylcellulose for 1 week under normoxic (20% oxygen) or hypoxic (1% oxygen) conditions in media ± doxycycline (Dox) and GFP expression analyzed by flow cytometry. (B) Kaplan-Meier survival curve of mice transplanted with MLL-AF9–expressing cells (Hif-1αΔ/Δ, n = 6; Hif-1αfl/fl, n = 7). The log-rank (Mantel-Cox) test was used to assess statistical significance. The development of the disease was measured by the percentage of transduced cells (GFP+) (C) and myeloid cells (Gr1+ and/or Mac1+) (D) in PB 3, 7, and 10 weeks after transplantation (n = 10). At 12 weeks after transplantation, a set of mice was sacrificed and the phenotype of the disease analyzed by measuring several parameters: WBC (E), GFP+ cells (F), and myeloid cells (Gr1+ and/or Mac1+) (G) in BM, and spleen and spleen and liver weights (H) (n = 3). Plots and columns represent mean ± SEM. Two-tailed Student t test was used to assess statistical significance.

MLL-induced leukemia initiation/progression is independent of HIF-1α status, although MLL signals directly toward HIF. (A) GFP expression of a clone derived from doxycycline-inducible MLL-ENL BM cells transduced with a GFP-hypoxic reporter. Cells from this clone were grown in methylcellulose for 1 week under normoxic (20% oxygen) or hypoxic (1% oxygen) conditions in media ± doxycycline (Dox) and GFP expression analyzed by flow cytometry. (B) Kaplan-Meier survival curve of mice transplanted with MLL-AF9–expressing cells (Hif-1αΔ/Δ, n = 6; Hif-1αfl/fl, n = 7). The log-rank (Mantel-Cox) test was used to assess statistical significance. The development of the disease was measured by the percentage of transduced cells (GFP+) (C) and myeloid cells (Gr1+ and/or Mac1+) (D) in PB 3, 7, and 10 weeks after transplantation (n = 10). At 12 weeks after transplantation, a set of mice was sacrificed and the phenotype of the disease analyzed by measuring several parameters: WBC (E), GFP+ cells (F), and myeloid cells (Gr1+ and/or Mac1+) (G) in BM, and spleen and spleen and liver weights (H) (n = 3). Plots and columns represent mean ± SEM. Two-tailed Student t test was used to assess statistical significance.

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