Fig. 7.
Fig. 7. Comparison of ploidy distribution of MKs and the expression of CD41b in different ploidy classes in the MKs obtained in the presence of PEG-rHuMGDF or the combination of IL-3, SCF, and IL-6 from CD34+ CD41+ cells. Marrow CD34+ CD41+ cells were grown from 6 days in serum-free conditions, in the presence of PEG-rHuMGDF (10 ng/mL) or IL-3 (100 U/mL) plus SCF (50 ng/mL) plus IL-6 (100 U/mL). Ploidy of the CD41+ cells obtained in the presence of PEG-rHuMGDF (A) and IL-3 plus SCF plus IL-6 (B). Comparison of the expression of CD41b in MK cultivated in the presence of PEG-rHuMGDF (solid line) and the combination of IL-3, SCF and IL-6 (broken lines) in the 2N (C), 4N (D), 8N (E), 16N (F), and 32N MKs (G). MKs were considered as CD41b+ cells and analysis was performed in each ploidy class.

Comparison of ploidy distribution of MKs and the expression of CD41b in different ploidy classes in the MKs obtained in the presence of PEG-rHuMGDF or the combination of IL-3, SCF, and IL-6 from CD34+ CD41+ cells. Marrow CD34+ CD41+ cells were grown from 6 days in serum-free conditions, in the presence of PEG-rHuMGDF (10 ng/mL) or IL-3 (100 U/mL) plus SCF (50 ng/mL) plus IL-6 (100 U/mL). Ploidy of the CD41+ cells obtained in the presence of PEG-rHuMGDF (A) and IL-3 plus SCF plus IL-6 (B). Comparison of the expression of CD41b in MK cultivated in the presence of PEG-rHuMGDF (solid line) and the combination of IL-3, SCF and IL-6 (broken lines) in the 2N (C), 4N (D), 8N (E), 16N (F), and 32N MKs (G). MKs were considered as CD41b+ cells and analysis was performed in each ploidy class.

Close Modal

or Create an Account

Close Modal
Close Modal