Table 6.

Percentage of JAK2V617F mutation in the cDNA of CD34+ progenitor cells and their differentiated cellular progenies generated by SCF, IL-6, IL-3, and various dose of Epo




Following 12 days of culture with SCF ± IL-6 ± IL-3 plus different concentrations of Epo
Donors*
CD34+ cells before culture, %
0 U/mL, %
0.025 U/mL, %
0.1 U/mL, %
0.5 U/mL, %
4 U/mL, %
PV2   34.6   32.4   29.5   17.0   4.9   5.1  
PV4   71.0   49.3   35.6   19.1   9.8   12.1  
PV7   71.0   65.9   40.1   18.9   10.7   9.8  
PV8
 
76.6
 
71.4
 
70.1
 
57.9
 
46.4
 
53.1
 



Following 12 days of culture with SCF ± IL-6 ± IL-3 plus different concentrations of Epo
Donors*
CD34+ cells before culture, %
0 U/mL, %
0.025 U/mL, %
0.1 U/mL, %
0.5 U/mL, %
4 U/mL, %
PV2   34.6   32.4   29.5   17.0   4.9   5.1  
PV4   71.0   49.3   35.6   19.1   9.8   12.1  
PV7   71.0   65.9   40.1   18.9   10.7   9.8  
PV8
 
76.6
 
71.4
 
70.1
 
57.9
 
46.4
 
53.1
 

The purity of the CD34+ cells was ≥95%. The CD34+ cells were cultured in the presence of SCF, IL-3, IL-6 and different concentrations of Epo for 12 days. Each value represents the JAK2V617F mutant allele/JAK2 total allele × 100 in the cDNA. JAK2V617F/JAK2total was calculated according to the mean ΔCt and the standard curve by real time quantitative PCR.

*

The G-CSF—mobilized healthy subject had 0% JAK2V617F mutation.

Close Modal

or Create an Account

Close Modal
Close Modal