Table 2.

Effect of Cell Cycle Progression Under IL-3-SCF-FL Stimulation on the Repopulating Activity of CD34+ Cells Initially Isolated in G0

Experiment Time in Culture Cell Cycle StatusCell Dose/Mouse (×106) % Chimerism (%CD45+)*
1   0 h  G0 1.0 52.2; 20.8; 68.7  
 36 h  G0 1.0  35.2; 38.1  
  G1 1.0  1.6; 0.2  
2   0 h G0 0.7  12.0; 18.0  
 36 h G0 0.7  5.2; 9.15  
  G1 0.7  <0.1; <0.1  
  Total  0.7  <0.1; 0.4 
3   0 h  G0 0.7  12.9  
 36 h Total  0.7  1.5; 3.4 
Experiment Time in Culture Cell Cycle StatusCell Dose/Mouse (×106) % Chimerism (%CD45+)*
1   0 h  G0 1.0 52.2; 20.8; 68.7  
 36 h  G0 1.0  35.2; 38.1  
  G1 1.0  1.6; 0.2  
2   0 h G0 0.7  12.0; 18.0  
 36 h G0 0.7  5.2; 9.15  
  G1 0.7  <0.1; <0.1  
  Total  0.7  <0.1; 0.4 
3   0 h  G0 0.7  12.9  
 36 h Total  0.7  1.5; 3.4 

NOD/SCID mice were transplanted with indicated cell doses of freshly isolated (0 h) G0CD34+ cells or with CD34+ cells initially isolated in G0 and either remaining in G0 or progressing into G1 after 36 hours of ex vivo culture under IL-3-SCF-FL stimulation, as shown in Fig5. In experiments 2 and 3, the total represents CD34+ cells isolated in G0, cultured for 36 hours, and directly assayed for NOD/SCID repopulating capacity without restaining with Hst/PY and cell cycle fractionation.

*

Percentage of CD45+ cells are indicated for each recipient mouse 6 weeks posttransplantation.

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