Table 3.

Addition of an anti–SDF-1 antibody or SDF-1 antagonist to previously activated LTCs of normal bone marrow cells prevents the return of the primitive CFCs in the adherent layer to a quiescent state 4 to 5 days later

AdditionKilled by 3H-thymidine (%)
Primitive BFU-EsCFU-GMs
PrimitiveMature
None 0 ± 4 4 ± 5 43 ± 2 
Anti–SDF-1 antibody 36 ± 3 44 ± 4 38 ± 3 
Control antibody 0 ± 8 12 ± 6 44 ± 2  
SDF-1 (G2) 49 ± 3 51 ± 5 38 ± 1 
AdditionKilled by 3H-thymidine (%)
Primitive BFU-EsCFU-GMs
PrimitiveMature
None 0 ± 4 4 ± 5 43 ± 2 
Anti–SDF-1 antibody 36 ± 3 44 ± 4 38 ± 3 
Control antibody 0 ± 8 12 ± 6 44 ± 2  
SDF-1 (G2) 49 ± 3 51 ± 5 38 ± 1 

Anti-SDF-1 (and control antibody) were added at 30 μg/mL, and SDF-1(G2) was added at 10 μg/mL. Results shown are the mean ± SEM of data from 4 independent experiments. Both the anti–SDF-1 antibody and SDF-1(G2) had a significant effect compared with no addition (P < .001) or control antibody (P < .01) on the cycling of the primitive BFU-Es and primitive CFU-GMs, but not on the mature CFU-GMs (P > .05). The total colony counts in the control groups (no3H-thymidine) ranged from 14 to 134.

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