Figure 6
Figure 6. Pre-B cells from Arf−/− but not Ink4a−/− mice can initiate B-ALL. (A) Pro-B and pre-B cells from wild-type (4), Arf−/− (n = 2), and Ink4a−/− (n = 2) mice were purified, transduced with retroviral vectors containing GFP only or BCR-ABL/GFP and 2.0 × 104 cells were seeded in a single well in culture. The number of cells harvested 7 days later is indicated. (B) Pre-B cells were isolated from the bone marrow of wild-type (n = 2), Ink4a−/− (n = 2), or Arf−/− (n = 2) mice, transduced with BCR-AB/GFPL, and 80 000 cells were transplanted into 3 Rag1−/− recipients per group. All recipients of the Arf−/− pre-B cells developed B-lineage leukemia by day 22 posttransplantation, whereas wild-type or Ink4a−/− pre-B cells showed no signs of disease.

Pre-B cells from Arf−/− but not Ink4a−/− mice can initiate B-ALL. (A) Pro-B and pre-B cells from wild-type (4), Arf−/− (n = 2), and Ink4a−/− (n = 2) mice were purified, transduced with retroviral vectors containing GFP only or BCR-ABL/GFP and 2.0 × 104 cells were seeded in a single well in culture. The number of cells harvested 7 days later is indicated. (B) Pre-B cells were isolated from the bone marrow of wild-type (n = 2), Ink4a−/− (n = 2), or Arf−/− (n = 2) mice, transduced with BCR-AB/GFPL, and 80 000 cells were transplanted into 3 Rag1−/− recipients per group. All recipients of the Arf−/− pre-B cells developed B-lineage leukemia by day 22 posttransplantation, whereas wild-type or Ink4a−/− pre-B cells showed no signs of disease.

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