Fig. 7.
Fig. 7. Kinetics of IgG secretion, apoptosis, and IL6-R (CD126) expression. After thawing (RP5), CD20+cells were removed and the population was separated into CD138+ and CD138− cells. (A) CD20− CD138− cells were cultured in RPMI 1640 10% FCS with 3 ng/mL IL-6 for 7 days. At days 0, 1, 2, and 7, supernatant was harvested and the amount of secreted Ig was determined by ELISA. The number of viable cells was determined by trypan-blue exclusion. (B and C) CD20− CD138+cells (B) and CD20− CD138− (C) cells were cultured in RPMI 1640 10% FCS with 3 ng/mL IL-6. Apoptotic cells were determined by Apo2.7-PE staining. CD138-PECY5 and CD126-PE expression was determined in double staining in the viable cell population (R1 dot-plot FSC v SSC).

Kinetics of IgG secretion, apoptosis, and IL6-R (CD126) expression. After thawing (RP5), CD20+cells were removed and the population was separated into CD138+ and CD138 cells. (A) CD20 CD138 cells were cultured in RPMI 1640 10% FCS with 3 ng/mL IL-6 for 7 days. At days 0, 1, 2, and 7, supernatant was harvested and the amount of secreted Ig was determined by ELISA. The number of viable cells was determined by trypan-blue exclusion. (B and C) CD20 CD138+cells (B) and CD20 CD138 (C) cells were cultured in RPMI 1640 10% FCS with 3 ng/mL IL-6. Apoptotic cells were determined by Apo2.7-PE staining. CD138-PECY5 and CD126-PE expression was determined in double staining in the viable cell population (R1 dot-plot FSC v SSC).

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