Table 1.

Erythroid progenitors are reduced in Cul4A+/- mice but not total bone marrow and erythroid precursors



No. of cells per femur ± SEM

Wild-type
Cul4A+/-
Total cells/femur, × 106  32.25 ± 2.23   28.67 ± 2.50  
CFU-Es/femur, × 104  1.85 ± 0.41   0.78 ± 0.15* 
Erythroid precursors/femur, × 106   
    Proerythroblasts   0.67 ± 0.11   0.33 ± 0.07  
    Basophilic erythroblasts   8.11 ± 0.87   7.32 ± 0.47  
    Late basophilic erythroblasts and polychromatophilic erythroblasts   1.93 ± 0.26   1.57 ± 0.10  
    Orthochromatophilic erythroblasts
 
3.59 ± 1.13
 
2.66 ± 0.29
 


No. of cells per femur ± SEM

Wild-type
Cul4A+/-
Total cells/femur, × 106  32.25 ± 2.23   28.67 ± 2.50  
CFU-Es/femur, × 104  1.85 ± 0.41   0.78 ± 0.15* 
Erythroid precursors/femur, × 106   
    Proerythroblasts   0.67 ± 0.11   0.33 ± 0.07  
    Basophilic erythroblasts   8.11 ± 0.87   7.32 ± 0.47  
    Late basophilic erythroblasts and polychromatophilic erythroblasts   1.93 ± 0.26   1.57 ± 0.10  
    Orthochromatophilic erythroblasts
 
3.59 ± 1.13
 
2.66 ± 0.29
 

Cells were isolated from the bone marrow of wild-type and Cul4A+/- mice. Total bone marrow cells were determined with a Beckman Coulter particle counter. CFU-E colonies were counted 3 days after initiation of the progenitor cell methylcellulose colony assay. Bone marrow cells were incubated with PE-conjugated anti-Ter119 and FITC-conjugated anti-CD71 antibodies. Using flow cytometry, 4 cell populations of erythroid precursors were defined with specific staining characteristics: proerythroblasts as Ter119med CD71high; basophilic erythroblasts as Ter119high CD71high; late basophilic erythroblasts and polychromatophilic erythroblasts as Ter119highCD71med; and orthochromatophilic erythroblasts as Ter119highCD71low. The data presented are from one representative experiment with 3 wild-type and 3 Cul4A+/- mice of 4 independent experiments. The data are the mean ± SEM.

*

P < .05.

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