Table 2.

Expression of Ras or Bcr/Abl permits in ECoM cell lines does not prevent differentiation

SampleTreatmentProgenitors (%)Granulocytes (%)Monocytes (%)
ECoM-G Parental + E2 99 0  
 Parental − E2 98 0  
 RAS + E2 98 2  
 RAS − E2 99  
 BCR/ABL + E2 98 2  
 BCR/ABL − E2 18 17 65 
ECoM-M Parental + E2 100 0  
 Parental − E2 98  
 RAS + E2 89 11  
 RAS − E2 95  
 BCR/ABL + E2 97 3  
 BCR/ABL − E2 96 
SampleTreatmentProgenitors (%)Granulocytes (%)Monocytes (%)
ECoM-G Parental + E2 99 0  
 Parental − E2 98 0  
 RAS + E2 98 2  
 RAS − E2 99  
 BCR/ABL + E2 98 2  
 BCR/ABL − E2 18 17 65 
ECoM-M Parental + E2 100 0  
 Parental − E2 98  
 RAS + E2 89 11  
 RAS − E2 95  
 BCR/ABL + E2 97 3  
 BCR/ABL − E2 96 

Derivatives of ECoM-G and ECoM-M cells were established by retroviral infection with constructs encoding H-RasL61 or Bcr/Ablp190 followed by culture in the absence of GM-CSF. Granulocytic or monocytic differentiation, 7 days following the removal of estrogen, was assessed on the basis of morphology from Wright-Giemsa–stained cytocentrifuge preparations (minimum of 200 cells/sample).