Figure 3
Figure 3. KLF7 overexpression inhibits bone marrow reconstitution. (A) Bone marrow cells transduced with MSCV expressing KLF7 or vector alone were transplanted into lethally irradiated recipients, and peripheral blood was analyzed 6 and 12 weeks after transplantation. Transduction efficiency was determined by measuring the percentage of GFP+ KLS cells just before transplantation (72 hours after viral exposure, time = 0). Data represent 2 individual experiments with 3-5 mice per genotype per experiment. *P < .001. (B) Shown is the percentage of donor B cells (B220+), T cells (CD3e+), and neutrophils (Gr-1 high) that were GFP+ from 1 representative experiment. *P < .01. (C) Bone marrow cells were transduced with HIV-MND–expressing KLF7 or vector alone at a low multiplicity of infection were transplanted into irradiated congenic recipients and the percentage GFP+ leukocytes in the blood measured. Data represent 3 independent experiments. *P < .001. **P < .05. (D) The percentage of donor B cells (B220+), T cells (CD3e+), and neutrophils (Gr-1 high) that were GFP+ at 6 weeks after transplantation. *P < .05. **P < .01. ***P < .0001. (E) GFP+ cells were sorted 72 hours after viral transduction and RNA analyzed by real-time RT-PCR for KLF7 expression. Data are normalized to β-actin and represent 2 independent experiments. *P = .043. (F) To assess homing, GFP+ KLS cells were transplanted into irradiated recipients and the number of GFP+ cells recovered from the bone marrow 20 hours later determined. Shown are the number of GFP+ cells per 106 whole bone marrow cells, corrected for the number of cells injected. Data represent 3 individual experiments, with 3-6 mice per condition.

KLF7 overexpression inhibits bone marrow reconstitution. (A) Bone marrow cells transduced with MSCV expressing KLF7 or vector alone were transplanted into lethally irradiated recipients, and peripheral blood was analyzed 6 and 12 weeks after transplantation. Transduction efficiency was determined by measuring the percentage of GFP+ KLS cells just before transplantation (72 hours after viral exposure, time = 0). Data represent 2 individual experiments with 3-5 mice per genotype per experiment. *P < .001. (B) Shown is the percentage of donor B cells (B220+), T cells (CD3e+), and neutrophils (Gr-1 high) that were GFP+ from 1 representative experiment. *P < .01. (C) Bone marrow cells were transduced with HIV-MND–expressing KLF7 or vector alone at a low multiplicity of infection were transplanted into irradiated congenic recipients and the percentage GFP+ leukocytes in the blood measured. Data represent 3 independent experiments. *P < .001. **P < .05. (D) The percentage of donor B cells (B220+), T cells (CD3e+), and neutrophils (Gr-1 high) that were GFP+ at 6 weeks after transplantation. *P < .05. **P < .01. ***P < .0001. (E) GFP+ cells were sorted 72 hours after viral transduction and RNA analyzed by real-time RT-PCR for KLF7 expression. Data are normalized to β-actin and represent 2 independent experiments. *P = .043. (F) To assess homing, GFP+ KLS cells were transplanted into irradiated recipients and the number of GFP+ cells recovered from the bone marrow 20 hours later determined. Shown are the number of GFP+ cells per 106 whole bone marrow cells, corrected for the number of cells injected. Data represent 3 individual experiments, with 3-6 mice per condition.

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