Table 3.

Clonogenic assay for cord blood samples in the presence of BIBR1532




BFU-E

CFU-GM

Total count
Negative control   128 ± 111   13 ± 8   138 ± 117  
DMSO   126 ± 82   24 ± 14   148 ± 90  
10 μM   114 ± 98   12 ± 8   125 ± 105  
30 μM   133 ± 78   24 ± 13   155 ± 86  
50 μM   120 ± 67   25 ± 13   144 ± 75  
80 μM
 
132 ± 82
 
22 ± 11
 
152 ± 89
 



BFU-E

CFU-GM

Total count
Negative control   128 ± 111   13 ± 8   138 ± 117  
DMSO   126 ± 82   24 ± 14   148 ± 90  
10 μM   114 ± 98   12 ± 8   125 ± 105  
30 μM   133 ± 78   24 ± 13   155 ± 86  
50 μM   120 ± 67   25 ± 13   144 ± 75  
80 μM
 
132 ± 82
 
22 ± 11
 
152 ± 89
 

CD34+ cord blood cells (n = 7) were harvested from suspension culture by day 10, and cultured in serum-free methylcellulose medium supplemented with cytokines (SCF, GM-CSF, G-CSF, IL-3, IL-6, and erythropoietin [EPO]) and with increasing concentrations of BIBR1532 for 14 days. Experiments for each individual specimen were performed in triplicate.

Note: There is no significant difference observed in number or type of colonies at day 14 for those cultured with up to 80 μM BIBR1532 compared with the controls.

BFU-E indicates burst-forming unit erythroid; CFU-GM, colony-forming unit granulocyte/monocyte.

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