Figure 2.
Figure 2. Differences in CXCR4 expression, SDF-1–induced migration, and irradiation requirement between precursor-B ALL and CD34+ cells. (A) Precursor-B ALL cell line cells (5-20 × 106) were injected into NOD/SCID mice, either untreated (▪) or 48 hours after total body irradiation (375 cGy; ▦). The total number (average ± SE of at least 3 experiments) of human cells that homed to the murine BM 16 hours after transplantation is shown. This was calculated according to the number of human cells per 106 MNCs acquired by flow cytometry multiplied by the total number of MNCs in the BM. *P < .05 compared with homing into nonirradiated mice. (B) Fold increase (compared with migration to 125 ng/mL SDF-1) of spontaneous or SDF-1–induced migration (at the indicated concentrations) of precursor-B ALL (□; G2, Nalm-6, BRE cells; average ± SE of at least 3 experiments performed in duplicates for each cell line) and normal CB (▪) or MPB (▦) CD34+ cells. *P < .05 relative to migration toward 125 ng/mL SDF-1. (C) Immunofluorescence detection of intracellular (gray line), cell surface (black line), or isotype control (dotted line) expression of CXCR4 levels of normal CD34+ cells, G2 cells, or precursor-B ALL cells from patients with newly diagnosed disease (patient nos. 1, 3, 4, and 5). Representative experiments of at least 3 independent experiments for each group are shown.

Differences in CXCR4 expression, SDF-1–induced migration, and irradiation requirement between precursor-B ALL and CD34+ cells. (A) Precursor-B ALL cell line cells (5-20 × 106) were injected into NOD/SCID mice, either untreated (▪) or 48 hours after total body irradiation (375 cGy; ▦). The total number (average ± SE of at least 3 experiments) of human cells that homed to the murine BM 16 hours after transplantation is shown. This was calculated according to the number of human cells per 106 MNCs acquired by flow cytometry multiplied by the total number of MNCs in the BM. *P < .05 compared with homing into nonirradiated mice. (B) Fold increase (compared with migration to 125 ng/mL SDF-1) of spontaneous or SDF-1–induced migration (at the indicated concentrations) of precursor-B ALL (□; G2, Nalm-6, BRE cells; average ± SE of at least 3 experiments performed in duplicates for each cell line) and normal CB (▪) or MPB (▦) CD34+ cells. *P < .05 relative to migration toward 125 ng/mL SDF-1. (C) Immunofluorescence detection of intracellular (gray line), cell surface (black line), or isotype control (dotted line) expression of CXCR4 levels of normal CD34+ cells, G2 cells, or precursor-B ALL cells from patients with newly diagnosed disease (patient nos. 1, 3, 4, and 5). Representative experiments of at least 3 independent experiments for each group are shown.

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