Table 4.

Morphologic analysis of PB CD34+ cells isolated from patients with PV and healthy G-CSF–mobilized donors cultured in vitro for 6 days and 12 days




Myeloblast, %

Promyeloblast, %

Myelocyte, %

Metamyelocyte, %

Normoblasts, %
PV      
    Day 6   14.6 ± 4.1   61.3 ± 6.2   11.2 ± 8.2   2.3 ± 1.5   4.9 ± 4.1  
    Day 12   2.1 ± 1.7   31.0 ± 6.5   23.2 ± 10.0   18.4 ± 6.3   7.6 ± 4.3  
Mob      
    Day 6   10.9 ± 2.5   49.1 ± 5.1   35.5 ± 7.7   2.0 ± 1.0   2.5 ± 3.0  
    Day 12
 
2.5 ± 1.4
 
26.5 ± 4.9
 
41.3 ± 12.2
 
20.0 ± 6.8
 
9.7 ± 4.6
 



Myeloblast, %

Promyeloblast, %

Myelocyte, %

Metamyelocyte, %

Normoblasts, %
PV      
    Day 6   14.6 ± 4.1   61.3 ± 6.2   11.2 ± 8.2   2.3 ± 1.5   4.9 ± 4.1  
    Day 12   2.1 ± 1.7   31.0 ± 6.5   23.2 ± 10.0   18.4 ± 6.3   7.6 ± 4.3  
Mob      
    Day 6   10.9 ± 2.5   49.1 ± 5.1   35.5 ± 7.7   2.0 ± 1.0   2.5 ± 3.0  
    Day 12
 
2.5 ± 1.4
 
26.5 ± 4.9
 
41.3 ± 12.2
 
20.0 ± 6.8
 
9.7 ± 4.6
 

The purity of the CD34+ cells was 95% or greater. The CD34+ cells were cultured in the presence of SCF, IL-3, IL-6, and Epo at their optimal concentration for 12 days. Cytospin preparations of the cells (day 6 and day 12) were prepared and stained with May-Grünwald-Giemsa. A 100- to 200-cell differential was performed under × 400 magnification using an Olympus BH-2 light microscope. Data are presented as mean ± SD.

Mob indicates G-CSF—mobilized healthy subject.

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