Fig. 7.
Fig. 7. LasBD suppresses BCR/ABL mRNA in primary CML cells and renders normal and CML progenitors MTX-resistant. (A) 1 × 104 normal or CML CD34+ HLA-DR+ cells were transduced with LasBD or the control vector, LBD containing PA317 supernatants, protamine sulfate, IL-3, IL-6, and SCF in contact with M2-10B4 stromal feeders for 24 hours. Cells were subsequently cultured in serum-free semisolid methylcellulose culture in the presence or absence of 5 × 10−8 mol/L MTX to determine the percentage of MTX-resistant progenitors. Results are represented as the percentage of CFC surviving 5 × 10−8 mol/L MTX from 2 patients with CML (with known b3a2 breakpoint) and 3 normal individuals. (B) 5 × 104 LasBD and LBD-transduced CML CD34+ HLA-DR+ cells were cultured for 14 days in liquid serum-free culture containing 5 × 10−8 mol/L MTX and cells examined by RT-PCR for the presence of the BCR/ABL mRNA.

LasBD suppresses BCR/ABL mRNA in primary CML cells and renders normal and CML progenitors MTX-resistant. (A) 1 × 104 normal or CML CD34+ HLA-DR+ cells were transduced with LasBD or the control vector, LBD containing PA317 supernatants, protamine sulfate, IL-3, IL-6, and SCF in contact with M2-10B4 stromal feeders for 24 hours. Cells were subsequently cultured in serum-free semisolid methylcellulose culture in the presence or absence of 5 × 10−8 mol/L MTX to determine the percentage of MTX-resistant progenitors. Results are represented as the percentage of CFC surviving 5 × 10−8 mol/L MTX from 2 patients with CML (with known b3a2 breakpoint) and 3 normal individuals. (B) 5 × 104 LasBD and LBD-transduced CML CD34+ HLA-DR+ cells were cultured for 14 days in liquid serum-free culture containing 5 × 10−8 mol/L MTX and cells examined by RT-PCR for the presence of the BCR/ABL mRNA.

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