Proliferation Rate of G0CD34+ Cells Isolated Before and After Ex Vivo Expansion
Cell Phenotype . | % Cells in S/G2 + M at Indicated . | ||
---|---|---|---|
. | Time (h) After Isolation . | ||
. | 0 . | 24 . | 48 . |
G0CD34+ | 1.45 ± 0.523-150 | 2.61 ± 1.41† | 12.73 ± 3.383-150 |
G0CD34+PKH2dim | 2.55 ± 0.873-150 | 14.24 ± 5.36† | 11.31 ± 2.373-150 |
Cell Phenotype . | % Cells in S/G2 + M at Indicated . | ||
---|---|---|---|
. | Time (h) After Isolation . | ||
. | 0 . | 24 . | 48 . |
G0CD34+ | 1.45 ± 0.523-150 | 2.61 ± 1.41† | 12.73 ± 3.383-150 |
G0CD34+PKH2dim | 2.55 ± 0.873-150 | 14.24 ± 5.36† | 11.31 ± 2.373-150 |
Cultures were initiated with freshly isolated BM G0CD34+ cells and G0CD34+PKH2dim cells at day 7 isolated from paired samples as illustrated in Fig 7. Both cultures were supported with 100 ng/mL each of IL-3, IL-6, and SCF in complete medium. At initiation and at 24-hour intervals, samples were assayed for cell-cycle analysis by the propidium iodide method. Results are expressed as the mean ± SEM, n = 3.
P > .05, † P < .05: paired t-tests.