Fig. 5.
Fig. 5. Sorting of p14+ and p14−cells present after long-term culture with FLT3-L plus TPO. Ex vivo–sorted CD34+ cord blood cells were grown for 21 days in FLT3-L plus TPO, with an increase in total cell number of 110-fold and were frozen. Cells were thawed 3 months later and grown for 26 extra days in the same conditions, with an increase in total cell number of 12-fold, giving an overall proliferation of 1,320-fold. Cells were then sorted in either CD1a−CD14+CD34−(p14+) or CD1a−CD14−CD34−(p14−) with a cocktail of anti–CD1a-PE, anti–CD34-PE, and anti–CD14-FITC MoAbs and cultured for 3 days with GM-CSF and IL-4, GM-CSF, IL-4, and TNF or for 3 and 9 days with GM-CSF and TNF. These data are from one experiment representative of seven. Sorting cells from primary cultures at different time points produced similar results.

Sorting of p14+ and p14cells present after long-term culture with FLT3-L plus TPO. Ex vivo–sorted CD34+ cord blood cells were grown for 21 days in FLT3-L plus TPO, with an increase in total cell number of 110-fold and were frozen. Cells were thawed 3 months later and grown for 26 extra days in the same conditions, with an increase in total cell number of 12-fold, giving an overall proliferation of 1,320-fold. Cells were then sorted in either CD1aCD14+CD34(p14+) or CD1aCD14CD34(p14) with a cocktail of anti–CD1a-PE, anti–CD34-PE, and anti–CD14-FITC MoAbs and cultured for 3 days with GM-CSF and IL-4, GM-CSF, IL-4, and TNF or for 3 and 9 days with GM-CSF and TNF. These data are from one experiment representative of seven. Sorting cells from primary cultures at different time points produced similar results.

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