Table 4.

SDF-1 increases the percentage of PB Inc+CD34+ cells in the S + G2/M phases

Source of Cells Incubation Time (h)SDF-1 Treatment % of Cells in Cell Cycle Phases4-150 (Mean ± SD)
G0/G1S + G2/M
PB IncCD34+ 0   98.6 ± 0.8  1.4 ± 0.8 
 48  −  92.4 ± 0.6  7.6 ± 0.6  
  90.9 ± 1.3  8.6 ± 0.8  
 72  − 89.2 ± 2.6  9.4 ± 0.8  
  +  88.5 ± 4.1 9.2 ± 0.4  
PB Inc+ CD34+  98.3 ± 0.4  1.7 ± 0.4  
 48  − 87.8 ± 0.6  12.1 ± 0.6  
  +  66.8 ± 1.6 33.1 ± 1.64-151, 
 72  −  82.2 ± 1.2 16.8 ± 1.7  
  +  69.7 ± 1.8 30.1 ± 2.24-151, 
Source of Cells Incubation Time (h)SDF-1 Treatment % of Cells in Cell Cycle Phases4-150 (Mean ± SD)
G0/G1S + G2/M
PB IncCD34+ 0   98.6 ± 0.8  1.4 ± 0.8 
 48  −  92.4 ± 0.6  7.6 ± 0.6  
  90.9 ± 1.3  8.6 ± 0.8  
 72  − 89.2 ± 2.6  9.4 ± 0.8  
  +  88.5 ± 4.1 9.2 ± 0.4  
PB Inc+ CD34+  98.3 ± 0.4  1.7 ± 0.4  
 48  − 87.8 ± 0.6  12.1 ± 0.6  
  +  66.8 ± 1.6 33.1 ± 1.64-151, 
 72  −  82.2 ± 1.2 16.8 ± 1.7  
  +  69.7 ± 1.8 30.1 ± 2.24-151, 

PB CD34+ cells purified immediately after density gradient separation (Inc) or after incubation on a plastic support (Inc+) were cultured (1 × 105 cells/mL) in a serum- and cytokine-free medium with or without (control) SDF-1 (0.05 ng/mL). At various time points, cells were harvested by centrifugation, counted, stained with propidium iodide, and analyzed by flow cytometry.

F4-150

Based on three independent experiments.

F4-151

P = .004 versus SDF-1 untreated control cells.

P < .0001 versus Inc cells.

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