Fig. 4.
Fig. 4. Comparison of engraftment capacity of MPB CD34+ cells isolated in G0 or in G1 phase of the cell cycle. Data from four experiments are reported as the mean ± SEM. Each experiment was performed with MPB CD34+ cells isolated from a different donor (n = 2 to 4 animals per experiment). (A) Percentages of chimeric human CD45+ cells in the BM of mice transplanted 6 weeks previously with indicated numbers of G0 or G1CD34+ cells. Average chimerism was statistically higher after transplantation of G0CD34+ cells than after transplantation of G1CD34+ cells (P < .05, pairedt-test). (B) Numbers of human progenitor cells per 50 × 103 BM cells 6 weeks posttransplantation in the same recipient mice. Average human progenitor output was statistically higher in G0- versus G1-transplanted mice (P < .05, paired t-test).

Comparison of engraftment capacity of MPB CD34+ cells isolated in G0 or in G1 phase of the cell cycle. Data from four experiments are reported as the mean ± SEM. Each experiment was performed with MPB CD34+ cells isolated from a different donor (n = 2 to 4 animals per experiment). (A) Percentages of chimeric human CD45+ cells in the BM of mice transplanted 6 weeks previously with indicated numbers of G0 or G1CD34+ cells. Average chimerism was statistically higher after transplantation of G0CD34+ cells than after transplantation of G1CD34+ cells (P < .05, pairedt-test). (B) Numbers of human progenitor cells per 50 × 103 BM cells 6 weeks posttransplantation in the same recipient mice. Average human progenitor output was statistically higher in G0- versus G1-transplanted mice (P < .05, paired t-test).

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