Table 1.

Differentiation of 32Dcl3 cells is blocked by expression of FLT3/ITD

CellsDay 0Day 9
32D/pBabe32D/FLT332D/FLT3/ITD32D/pBabe32D/FLT332DFLT3/ITD
Myeloblasts, % 81.3 ± 2.5 85.7 ± 3.8 82.3 ± 4.5 14.3 ± 2.5 11.3 ± 3.2 85.3 ± 5.0 
Intermediates, % 18.7 ± 2.5 14.3 ± 3.8 17.7 ± 4.5 64 ± 3.6 66.7 ± 4.5 14.7 ± 5.0 
Granulocytes, % 0  0  21.7 ± 4.0 14.7 ± 5.0 
CellsDay 0Day 9
32D/pBabe32D/FLT332D/FLT3/ITD32D/pBabe32D/FLT332DFLT3/ITD
Myeloblasts, % 81.3 ± 2.5 85.7 ± 3.8 82.3 ± 4.5 14.3 ± 2.5 11.3 ± 3.2 85.3 ± 5.0 
Intermediates, % 18.7 ± 2.5 14.3 ± 3.8 17.7 ± 4.5 64 ± 3.6 66.7 ± 4.5 14.7 ± 5.0 
Granulocytes, % 0  0  21.7 ± 4.0 14.7 ± 5.0 

Differential counts of 32D/pBabe, 32D/FLT3, and 32D/FLT3/ITD cell cultures induced by G-CSF (20 ng/mL) were performed on days 0 and 9.

Values are the mean percentages, ± SD, of cells from 3 independent counts examined by light microscopy after Wright-Giemsa staining of the cytospins. “Intermediates” include promyelocytes, myelocytes, and metamyelocytes.

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