Figure 5.
Figure 5. Analysis of human genome and the percentage of hCD45 in NOD/SCID–ß2m–/– mice. Analysis of human genome and the percentage of hCD45 in NOD/SCID–ß2m–/– mice. (A) PCR amplification of human ALU sequences was performed to confirm the sequence found in the human genome. Mice (n = 3) with transplants of accessory cells only (lanes 1-3); mice (n = 5) with transplants of fresh CD34+ cells (lanes 4-7). The percentage of hCD45 indicates the percentage of the human CD45+ hematopoietic cells in the BM of mice with transplants. (B) Analyses of hCD45+ cells in the BM of NOD/SCID–ß2m–/– mice with transplants. Irradiated carrier cells, fresh CD34+ cells, or CD34+ cells that had been expanded on control stromal cells or Ihh stromal cells, were transplanted into NOD/SCID–ß2m–/– mice. Mice were killed 8 weeks after transplantation, and the BM cells were analyzed by flow cytometry. Data are shown for carrier cells; fresh CD34+ cells; CD34+ cells that had been expanded ex vivo in the absence of stromal cells for 2 weeks; CD34+ cells that had been expanded on control stromal cells for 2 weeks; CD34+ cells that had been expanded on control stromal cells for 2 weeks in the presence of anti-Ihh blocking Ab; CD34+ cells that had been expanded on Ihh stromal cells for 2 weeks; and CD34+ cells that had been expanded on Ihh stromal cells for 2 weeks in the presence of anti-Ihh blocking Ab. A dotted line indicates the cut-off level (0.1%) for successful engraftment of human hematopoietic cells. *P < .05 versus control stromal cells. **P < .05 versus Ihh stromal cells (Mann-Whitney U test). Data represent a summary of 2 separate experiments. (C) Engraftment of a graded dose of CD34+ cells at the start of culture and their progeny after 2 weeks. Percentage of engraftment of human CD45+ cells that had been expanded with control stromal cells (i), or Ihh stromal cells (ii) is shown. Dotted lines indicate cutoff level (0.1%).

Analysis of human genome and the percentage of hCD45 in NOD/SCID–ß2m–/– mice. Analysis of human genome and the percentage of hCD45 in NOD/SCID–ß2m–/– mice. (A) PCR amplification of human ALU sequences was performed to confirm the sequence found in the human genome. Mice (n = 3) with transplants of accessory cells only (lanes 1-3); mice (n = 5) with transplants of fresh CD34+ cells (lanes 4-7). The percentage of hCD45 indicates the percentage of the human CD45+ hematopoietic cells in the BM of mice with transplants. (B) Analyses of hCD45+ cells in the BM of NOD/SCID–ß2m–/– mice with transplants. Irradiated carrier cells, fresh CD34+ cells, or CD34+ cells that had been expanded on control stromal cells or Ihh stromal cells, were transplanted into NOD/SCID–ß2m–/– mice. Mice were killed 8 weeks after transplantation, and the BM cells were analyzed by flow cytometry. Data are shown for carrier cells; fresh CD34+ cells; CD34+ cells that had been expanded ex vivo in the absence of stromal cells for 2 weeks; CD34+ cells that had been expanded on control stromal cells for 2 weeks; CD34+ cells that had been expanded on control stromal cells for 2 weeks in the presence of anti-Ihh blocking Ab; CD34+ cells that had been expanded on Ihh stromal cells for 2 weeks; and CD34+ cells that had been expanded on Ihh stromal cells for 2 weeks in the presence of anti-Ihh blocking Ab. A dotted line indicates the cut-off level (0.1%) for successful engraftment of human hematopoietic cells. *P < .05 versus control stromal cells. **P < .05 versus Ihh stromal cells (Mann-Whitney U test). Data represent a summary of 2 separate experiments. (C) Engraftment of a graded dose of CD34+ cells at the start of culture and their progeny after 2 weeks. Percentage of engraftment of human CD45+ cells that had been expanded with control stromal cells (i), or Ihh stromal cells (ii) is shown. Dotted lines indicate cutoff level (0.1%).

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