Figure 6
Figure 6. Restoration of c-Myb expression rescues colony formation of c-Mybf/d p210BCR/ABL-transduced marrow progenitors. c-Mybf/d and c-Mybf/f Lin−Sca-1+Kit+ cells were transduced with the MigRI/p210BCR/ABL retrovirus and 24 hours after retroviral transduction sorted for GFP positivity. p210BCR/ABL-expressing c-Mybf/d Lin−Sca-1+Kit+ cells were subsequently transduced with a c-Myb/MSCV/puro retrovirus or the empty MSCV/puro vector as a negative control. p210BCR/ABL-expressing c-Mybf/f Lin−Sca-1+Kit+ cells were transduced with empty vector MSCV/puro as a positive control. After 24 hours, cells (8 × 104/plate) were plated in methylcellulose in the presence of puromycin (1 μg/mL). Colony formation was assessed 9 days later. Representative of 3 different experiments. P ≤ .001.

Restoration of c-Myb expression rescues colony formation of c-Mybf/d p210BCR/ABL-transduced marrow progenitors. c-Mybf/d and c-Mybf/f LinSca-1+Kit+ cells were transduced with the MigRI/p210BCR/ABL retrovirus and 24 hours after retroviral transduction sorted for GFP positivity. p210BCR/ABL-expressing c-Mybf/d LinSca-1+Kit+ cells were subsequently transduced with a c-Myb/MSCV/puro retrovirus or the empty MSCV/puro vector as a negative control. p210BCR/ABL-expressing c-Mybf/f LinSca-1+Kit+ cells were transduced with empty vector MSCV/puro as a positive control. After 24 hours, cells (8 × 104/plate) were plated in methylcellulose in the presence of puromycin (1 μg/mL). Colony formation was assessed 9 days later. Representative of 3 different experiments. P ≤ .001.

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