Fig. 7.
Fig. 7. CCR6 is not expressed during in vitro plasmablast differentiation of GC B cells. / (A) Phenotypic changes during the differentiation of GC B cells into plasmablasts in vitro. GC B cells purified by immunomagnetic cell sorting (> 90% cell viability) were cultured in the presence of IL-10, IL-2, IL-4, and anti-CD40 MoAb, as described in “Materials and methods.” At the indicated time points, CD38 and CD20 expression was determined by double staining with anti-CD38-PE and anti-CD20-FITC MoAbs. Note the progressive increase in the CD38highCD20− population corresponding to the plasmacytoid differentiation stage. Percentages of cells within each quadrant are indicated. (B) Analysis of CCR6 expression by double staining with anti-CD20-FITC and anti-CCR6-PE MoAbs during plasmablast differentiation is presented in panel A. One representative experiments of 3 using cells from different donors is shown.

CCR6 is not expressed during in vitro plasmablast differentiation of GC B cells.

(A) Phenotypic changes during the differentiation of GC B cells into plasmablasts in vitro. GC B cells purified by immunomagnetic cell sorting (> 90% cell viability) were cultured in the presence of IL-10, IL-2, IL-4, and anti-CD40 MoAb, as described in “Materials and methods.” At the indicated time points, CD38 and CD20 expression was determined by double staining with anti-CD38-PE and anti-CD20-FITC MoAbs. Note the progressive increase in the CD38highCD20 population corresponding to the plasmacytoid differentiation stage. Percentages of cells within each quadrant are indicated. (B) Analysis of CCR6 expression by double staining with anti-CD20-FITC and anti-CCR6-PE MoAbs during plasmablast differentiation is presented in panel A. One representative experiments of 3 using cells from different donors is shown.

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