Fig. 5.
Fig. 5. Exit from G0/G1 phases of cell cycle. / Exit from G0/G1 phases of cell cycle of total Sca-1+lin− cells (▴), or engrafting phenotypes (dotted lines) and nonengrafting phenotypes (solid lines) of Sca-1+lin− AM+ (▪) and AM− (○) cells. Up to 4 × 103 cells/mL were supplemented with 20% FBS, 2 × 10−5 mol/L 2-mercaptoethanol, 100 ng/mL mSCF and hIL6, 500 U/mL mIL1α, 100 U/mL mIL3, and 50 ng/mL hFlt3-L. Fresh cells and aliquots of cultured cells removed on days 1 and 2 were stained with propidium iodide and analyzed for cell cycle status as previously described.23 Data are expressed as the mean ± SEM; n = 2 to 3 for each time point. Slopes of linear regression lines generated from these data are indicated next to the appropriate lines to illustrate relative rates of exit from G0/G1 of the different populations of cells. *The presence of statistical significance in slope of regression line of engrafting phenotype when compared with the slope generated from its nonengrafting counterpart; P < .05.

Exit from G0/G1 phases of cell cycle.

Exit from G0/G1 phases of cell cycle of total Sca-1+lin cells (▴), or engrafting phenotypes (dotted lines) and nonengrafting phenotypes (solid lines) of Sca-1+lin AM+ (▪) and AM (○) cells. Up to 4 × 103 cells/mL were supplemented with 20% FBS, 2 × 10−5 mol/L 2-mercaptoethanol, 100 ng/mL mSCF and hIL6, 500 U/mL mIL1α, 100 U/mL mIL3, and 50 ng/mL hFlt3-L. Fresh cells and aliquots of cultured cells removed on days 1 and 2 were stained with propidium iodide and analyzed for cell cycle status as previously described.23 Data are expressed as the mean ± SEM; n = 2 to 3 for each time point. Slopes of linear regression lines generated from these data are indicated next to the appropriate lines to illustrate relative rates of exit from G0/G1 of the different populations of cells. *The presence of statistical significance in slope of regression line of engrafting phenotype when compared with the slope generated from its nonengrafting counterpart; P < .05.

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