Figure 7.
Figure 7. The in vivo phenotype conferred by Smad7 is dependent on Smad4. (A) GFP contribution in PB of primary recipients as assessed by FACS analysis at 13 weeks after BM transplantation: WT cells transduced with the MIG vector, 16.5% ± 5.0%; WT cells transduced with Smad7 vector, 31.6% ± 8.26%; Smad4–/– cells transduced with MIG vector, 6.19% ± 0.96%; Smad4–/– cells transduced with Smad7 vector, 7.97% ± 0.6%. (B) The percentage of GFP+ cells in PB of secondary recipients at 12 weeks after BM transplantation: WT cells transduced with MIG vector, 2.3% ± 0.51%; WT cells transduced with Smad7 vector, 62.2% ± 2.7%; Smad4–/– cells transduced with MIG vector, 0.2% ± 0.06%; Smad4–/– cells transduced with Smad7 vector, 0.2% ± 0.05%. Data are from 1 representative experiment and calculated as mean values ± SEM (P < .05 between WT/Smad7 and Smad4–/–/Smad7). A total of 20 primary and 16 secondary recipients were used.

The in vivo phenotype conferred by Smad7 is dependent on Smad4. (A) GFP contribution in PB of primary recipients as assessed by FACS analysis at 13 weeks after BM transplantation: WT cells transduced with the MIG vector, 16.5% ± 5.0%; WT cells transduced with Smad7 vector, 31.6% ± 8.26%; Smad4–/– cells transduced with MIG vector, 6.19% ± 0.96%; Smad4–/– cells transduced with Smad7 vector, 7.97% ± 0.6%. (B) The percentage of GFP+ cells in PB of secondary recipients at 12 weeks after BM transplantation: WT cells transduced with MIG vector, 2.3% ± 0.51%; WT cells transduced with Smad7 vector, 62.2% ± 2.7%; Smad4–/– cells transduced with MIG vector, 0.2% ± 0.06%; Smad4–/– cells transduced with Smad7 vector, 0.2% ± 0.05%. Data are from 1 representative experiment and calculated as mean values ± SEM (P < .05 between WT/Smad7 and Smad4–/–/Smad7). A total of 20 primary and 16 secondary recipients were used.

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