Fig. 1.
Fig. 1. Differentiation of peripheral blood B cells into polyclonal plasmablastic cells. / (A) Percentages of CD20−/CD38++ cells were evaluated on purified PB B cells, on unseparated cells obtained after the 2-step culture, and on sorted cells. Viable cells were gated by size and granulometry. (B) Giemsa staining of sorted CD20−/CD38++ cells showing their plasma cell morphology and a mitosis figure (arrow). Original magnification, × 1000. (C) Unseparated cells were stained with anti-κ (brown) and anti-λ (red) light chain. Original magnification, × 400. (D) Percentages of CD20−/CD38++ cells in the S-phase were determined using PI staining. They ranged from 24% to 36% in 5 separate experiments.

Differentiation of peripheral blood B cells into polyclonal plasmablastic cells.

(A) Percentages of CD20/CD38++ cells were evaluated on purified PB B cells, on unseparated cells obtained after the 2-step culture, and on sorted cells. Viable cells were gated by size and granulometry. (B) Giemsa staining of sorted CD20/CD38++ cells showing their plasma cell morphology and a mitosis figure (arrow). Original magnification, × 1000. (C) Unseparated cells were stained with anti-κ (brown) and anti-λ (red) light chain. Original magnification, × 400. (D) Percentages of CD20/CD38++ cells in the S-phase were determined using PI staining. They ranged from 24% to 36% in 5 separate experiments.

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