Table 2

Number of myeloid progenitors derived from PMF-purified CD34+ in methylcellulose medium

EECsTotal BFU-EsTotal CFU-GMs
PMF1 MPL W515L 82 
PMF2 MPL W515L 14 
PMF3 MPL W515K 55 185 
Mean PMF MPL W515 21 71 
PMF4 JAK2 V617F 84 136 
PMF5 JAK2 V617F 28 144 198 
PMF6 JAK2 V617F 21 17 
PMF7 JAK2 V617F 17 17 37 
PMF8 JAK2 V617F 11 10 
PMF9 JAK2 V617F 10 40 150 
Mean PMF JAK2 V617F 12 53 91 
P .015 .141 .387 
EECsTotal BFU-EsTotal CFU-GMs
PMF1 MPL W515L 82 
PMF2 MPL W515L 14 
PMF3 MPL W515K 55 185 
Mean PMF MPL W515 21 71 
PMF4 JAK2 V617F 84 136 
PMF5 JAK2 V617F 28 144 198 
PMF6 JAK2 V617F 21 17 
PMF7 JAK2 V617F 17 17 37 
PMF8 JAK2 V617F 11 10 
PMF9 JAK2 V617F 10 40 150 
Mean PMF JAK2 V617F 12 53 91 
P .015 .141 .387 

Peripheral blood CD34+ cells from PMF patients was seeded in methylcellulose in the presence or absence of Epo or G-CSF. Erythroid and granulocytic colonies were picked on day 14 and genotyped by SNP analysis.

EECs indicates endogenous erythroid colonies; BFU-Es, burst-forming units–erythroid; and CFU-GMs, colony-forming units–granulocyte-macrophage.

Close Modal

or Create an Account

Close Modal
Close Modal