Figure 2
Figure 2. CD38 expression in Ki-67+ and Ki-67− CLL cells and 2H enrichment in CLL clonal fractions sorted based on CD38 and Ki-67. (A) PBMCs from CLL 822 were incubated with fluorochrome-labeled mAbs reactive with CD19, CD5, and CD38, and, after cell permeabilization, with Ki-67. Cells were first gated for CD19 and then analyzed as reported in the figure. (Top plot) CLL clone contains ∼ 5% Ki-67+ cells. (Bottom plots) Percentage of CD38+ cells in the CD19+CD5+Ki-67+ fraction (83%; bottom right) is much higher compared with that observed in the CD19+CD5+Ki-67− fraction (18%; bottom left). CLL cells from CLL 452 (B) and CLL 625 (C) were flow-sorted based on CD38 and Ki-67 expression, and 2H-labeled DNA was measured in the sorted fractions. Curves represent the fraction (f) of labeled cells reported in the tables. Ki-67+ cells, both CD38− and CD38+, incorporated more 2H than their Ki-67− counterparts.

CD38 expression in Ki-67+ and Ki-67 CLL cells and 2H enrichment in CLL clonal fractions sorted based on CD38 and Ki-67. (A) PBMCs from CLL 822 were incubated with fluorochrome-labeled mAbs reactive with CD19, CD5, and CD38, and, after cell permeabilization, with Ki-67. Cells were first gated for CD19 and then analyzed as reported in the figure. (Top plot) CLL clone contains ∼ 5% Ki-67+ cells. (Bottom plots) Percentage of CD38+ cells in the CD19+CD5+Ki-67+ fraction (83%; bottom right) is much higher compared with that observed in the CD19+CD5+Ki-67 fraction (18%; bottom left). CLL cells from CLL 452 (B) and CLL 625 (C) were flow-sorted based on CD38 and Ki-67 expression, and 2H-labeled DNA was measured in the sorted fractions. Curves represent the fraction (f) of labeled cells reported in the tables. Ki-67+ cells, both CD38 and CD38+, incorporated more 2H than their Ki-67 counterparts.

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