Fig. 4.
Fig. 4. Flow cytometry analysis of the shedding of membrane microparticles from PNH (P) and control (T) RBC after calcium ionophore treatment. Dot plot representations of AVFITC-labeled cell and particle suspensions. Cells have the highest forward scatter signal (FSC), whereas derived microparticles have a lower one. The proportion of events in each gate is indicated. Stimulation was achieved by 5 μmol/L calcium ionophore A23187 in the presence of 2 mmol/L external CaCl2 for 90 minutes at 37°C. Fluorescence intensity reflects the extent of AVFITC labeling of the population of interest, testifying to the degree of phosphatidylserine externalization. Each dot plot corresponds to 10,000 events and is representative of three experiments performed likewise.

Flow cytometry analysis of the shedding of membrane microparticles from PNH (P) and control (T) RBC after calcium ionophore treatment. Dot plot representations of AVFITC-labeled cell and particle suspensions. Cells have the highest forward scatter signal (FSC), whereas derived microparticles have a lower one. The proportion of events in each gate is indicated. Stimulation was achieved by 5 μmol/L calcium ionophore A23187 in the presence of 2 mmol/L external CaCl2 for 90 minutes at 37°C. Fluorescence intensity reflects the extent of AVFITC labeling of the population of interest, testifying to the degree of phosphatidylserine externalization. Each dot plot corresponds to 10,000 events and is representative of three experiments performed likewise.

Close Modal

or Create an Account

Close Modal
Close Modal