Fig. 5.
Fig. 5. Lentivirus and MLV vectors transduce HSCs with similar efficiency. / Representative co-transduction assay of Lin− mouse BM cells co-transduced with MLV-GFP-VSV-G (M-GFP) and ecotropic-MLV-LacZ (MLV group) or lentivirus-GFP-VSV-G (L-GFP) and ecotropic-MLV-LacZ (lenti group). Lin− mouse BM cells were transduced for 24 hours without cytokines with medium changed at 0 and 12 hours or for 96 hours in IL-3, IL-6, and SCF with medium changed every 24 hours. After transduction, the cells were injected intoW/Wv recipients. Peripheral blood DNA from the recipients was analyzed 16 weeks after transplant for the presence of the proviruses by PCR, using GFP- and LacZ-specific primers. PCR of the VSV-G-EGFP provirus generates a 586-bp product, and PCR of the ecotropic-lacZ provirus generates a 289-bp product. DNA from the producer cell lines was used as a positive control, and DNA from an untransplanted mouse was used as a negative control. The mouse adult β-globin gene was amplified as an internal control. Phosphor Imager analysis confirmed that each sample had equivalent amounts of DNA.

Lentivirus and MLV vectors transduce HSCs with similar efficiency.

Representative co-transduction assay of Lin mouse BM cells co-transduced with MLV-GFP-VSV-G (M-GFP) and ecotropic-MLV-LacZ (MLV group) or lentivirus-GFP-VSV-G (L-GFP) and ecotropic-MLV-LacZ (lenti group). Lin mouse BM cells were transduced for 24 hours without cytokines with medium changed at 0 and 12 hours or for 96 hours in IL-3, IL-6, and SCF with medium changed every 24 hours. After transduction, the cells were injected intoW/Wv recipients. Peripheral blood DNA from the recipients was analyzed 16 weeks after transplant for the presence of the proviruses by PCR, using GFP- and LacZ-specific primers. PCR of the VSV-G-EGFP provirus generates a 586-bp product, and PCR of the ecotropic-lacZ provirus generates a 289-bp product. DNA from the producer cell lines was used as a positive control, and DNA from an untransplanted mouse was used as a negative control. The mouse adult β-globin gene was amplified as an internal control. Phosphor Imager analysis confirmed that each sample had equivalent amounts of DNA.

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