Table 7.

Bone Marrow Progenitor Cell Analysis ofmpl−/− IL-3−/− Mutant Mice

Genotype Progenitor Cells per 2.5 × 104 Bone Marrow Cells
Total GranulocyteGM Macrophage Eosinophil Megakaryocyte Meg/EErythroid Blast
Wild-type  90 ± 40  26 ± 2 16 ± 11  21 ± 14  1 ± 1  8 ± 5 3 ± 2  4 ± 6  11 ± 4 
mpl+/+ IL-3−/− 79 ± 20  23 ± 5  13 ± 1  13 ± 4 1 ± 2  6 ± 2  5 ± 2  7 ± 8  11 ± 5 
mpl−/− IL-3+/+ 35 ± 13  8 ± 3  8 ± 8  9 ± 1  2 ± 2 3 ± 2  3 ± 2  1 ± 1  1 ± 1 
mpl−/− IL-3−/− 27 ± 8  8 ± 5  7 ± 4  6 ± 4  1 ± 1 2 ± 2  2 ± 1  1 ± 1  
Genotype Progenitor Cells per 2.5 × 104 Bone Marrow Cells
Total GranulocyteGM Macrophage Eosinophil Megakaryocyte Meg/EErythroid Blast
Wild-type  90 ± 40  26 ± 2 16 ± 11  21 ± 14  1 ± 1  8 ± 5 3 ± 2  4 ± 6  11 ± 4 
mpl+/+ IL-3−/− 79 ± 20  23 ± 5  13 ± 1  13 ± 4 1 ± 2  6 ± 2  5 ± 2  7 ± 8  11 ± 5 
mpl−/− IL-3+/+ 35 ± 13  8 ± 3  8 ± 8  9 ± 1  2 ± 2 3 ± 2  3 ± 2  1 ± 1  1 ± 1 
mpl−/− IL-3−/− 27 ± 8  8 ± 5  7 ± 4  6 ± 4  1 ± 1 2 ± 2  2 ± 1  1 ± 1  

Mean ± standard deviations of colony numbers in replicate cultures stimulated with the combination of SCF, IL-3, and EPO from 3 mice per genotype. Cultures were incubated in 5% CO2 in air for 7 days. Colony numbers and composition were determined by examination of stained cultures at 200× magnification. There were no significant differences for comparison of data frommpl+/+ IL-3−/− mice with wild-type mice, or for comparison of data frommpl−/− IL-3−/− mice withmpl−/− IL-3+/+ mice (P > .1).

Abbreviations: GM, mixed granulocyte/macrophage; Meg/E, mixed megakaryocyte/erythroid.

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