Fig. 5.
Fig. 5. Loss of cell viability in primary AML blasts after overnight culture. / Apoptotic cell death was determined by flow cytometry using 7-AAD. (A) Dose-response curve for mClCCP. The data plotted represent the mean (SD) value from 5 different cases analyzed in separate experiments. (B) Dot plots for an individual case. Two gated regions are shown. R3 encompasses cells with high forward scatter that exclude 7-AAD (viable cells). Apoptotic cells, which take up 7-AAD and have a reduced forward scatter, indicative of shrinking, are shown in R4. (i) Control cells (21% in R4). (ii) Cells cultured overnight with 30 μM mClCCP (59% in R4). (C) The mClCCP IC50 for 12 AML cases plotted against the percentage of cells that did not survive 21 to 23 hours of suspension culture without added growth factors.

Loss of cell viability in primary AML blasts after overnight culture.

Apoptotic cell death was determined by flow cytometry using 7-AAD. (A) Dose-response curve for mClCCP. The data plotted represent the mean (SD) value from 5 different cases analyzed in separate experiments. (B) Dot plots for an individual case. Two gated regions are shown. R3 encompasses cells with high forward scatter that exclude 7-AAD (viable cells). Apoptotic cells, which take up 7-AAD and have a reduced forward scatter, indicative of shrinking, are shown in R4. (i) Control cells (21% in R4). (ii) Cells cultured overnight with 30 μM mClCCP (59% in R4). (C) The mClCCP IC50 for 12 AML cases plotted against the percentage of cells that did not survive 21 to 23 hours of suspension culture without added growth factors.

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