Table 1

Hematopoietic progenitors in SCL+/D and SCL−/D mice

Tissue/genotypeNo. of colonies*
BFU-EGGMMMegBlastMast
Bone marrow        
    +/Δ 10 ± 3 14 ± 4 31 ± 12 18 ± 6 8 ± 4 3 ± 1 4 ± 2 
    −/Δ 0 17 ± 7 19 ± 5 12 ± 3 1 ± 1 3 ± 1 50 ± 13 
Spleen        
    +/Δ 2 ± 1 4 ± 1 4 ± 3 4 ± 3 2 ± 1 2 ± 1 
    −/Δ 7 ± 2 6 ± 3 3 ± 2 4 ± 1 66 ± 25 
Tissue/genotypeNo. of colonies*
BFU-EGGMMMegBlastMast
Bone marrow        
    +/Δ 10 ± 3 14 ± 4 31 ± 12 18 ± 6 8 ± 4 3 ± 1 4 ± 2 
    −/Δ 0 17 ± 7 19 ± 5 12 ± 3 1 ± 1 3 ± 1 50 ± 13 
Spleen        
    +/Δ 2 ± 1 4 ± 1 4 ± 3 4 ± 3 2 ± 1 2 ± 1 
    −/Δ 7 ± 2 6 ± 3 3 ± 2 4 ± 1 66 ± 25 

Twenty-five-thousand cells cultured for 7 days in 0.3% agar with IL-3, SCF, and MGDF or methylcellulose with IL-3, SCF, and Epo.

BFU-E indicates blast-forming unit-erythroid; G, granulocyte colonies; GM, granulocyte-macrophage colonies; M, macrophage colonies; and Meg, megakaryocyte colonies.

*

The numbers of colonies are the mean plus or minus SD from 4 mice of each genotype: SCL heterozygous (+/Δ,) and SCL deleted (−/Δ).

BFU-Es were grown in methylcellulose, while all other colonies were grown in agar.

Statistical comparison with SCL-heterozygous cells using Student t test; P < .05.

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