Table 2.

Prolonged Exposure to KL + IL-3 + IL-6, But Not KL + FL + MGDF, Deplete ELTC-CFC

Experiment No. Cytokines12-wk LTC-CFC, % of Control
d7 d12
K36  9 (16)  3 (5)  
 KF3  171 (28)  291 (267) 
 KFM  529 (193)  1,568 (268)  
2  K36  16 (15) 33 (19)  
 KF3  202 (147)  68 (84)  
 KFM 44 (38)  269 (88)  
3  K36  17 (30)  53 (91) 
 KF3  156 (136)  158 (80)  
 KFM  64 (50) 777 (874)  
4  K36  0   0   
 KF3 1,217 (507)  2,136 (1,176)  
 KFM  1,589 (404) 3,002 (1,331) 
Experiment No. Cytokines12-wk LTC-CFC, % of Control
d7 d12
K36  9 (16)  3 (5)  
 KF3  171 (28)  291 (267) 
 KFM  529 (193)  1,568 (268)  
2  K36  16 (15) 33 (19)  
 KF3  202 (147)  68 (84)  
 KFM 44 (38)  269 (88)  
3  K36  17 (30)  53 (91) 
 KF3  156 (136)  158 (80)  
 KFM  64 (50) 777 (874)  
4  K36  0   0   
 KF3 1,217 (507)  2,136 (1,176)  
 KFM  1,589 (404) 3,002 (1,331) 

One thousand to 1,500 human CD34+CD38cells were cultured in SF-medium in the presence of the indicated cytokines. As a control for the content of ELTC-IC in freshly isolated CD34+CD38 cells, the same number of cells was transferred directly to pre-established irradiated stroma. After 12 weeks of stroma cocultivation, the number of CFC produced was evaluated in methylcellulose cultures. Results are presented as the mean (SD) of triplicate wells per group and time point. Controls (fresh, nonexpanded CD34+CD38 cells) were set to represent 100% and reflected 55 ± 7 colonies in experiment no. 1, 40 ± 15 colonies in experiment no. 2, 11 ± 10 colonies in experiment no. 3, and 9 ± 5 colonies in experiment no. 4.

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