Fig. 5.
Fig. 5. CD40L culture enhances the proliferation of HB-LTC–derived CD19+ progenitors. A representative experiment in which CD19+ progenitors from an 8-week-old HB-LTC were seeded in microwells (105 cells/well) containing S17 stromal cells or CD40L fibroblasts in medium containing no added cytokines, IL-4, IL-10, or both cytokines. (A) Cell recovery was determined by trypan blue dye exclusion and expressed as the mean number of viable cells. (B) Cell cycle analysis of CD19+cells removed from the CD40L system. (Left) Dot plot of IgM versus DNA content analyzed by propidium iodide staining. (Right) Histogram illustrating DNA content in the IgM+ (R1) versus the IgM− (R2) populations. Numbers indicate the percentage of cells in S/G2/M.

CD40L culture enhances the proliferation of HB-LTC–derived CD19+ progenitors. A representative experiment in which CD19+ progenitors from an 8-week-old HB-LTC were seeded in microwells (105 cells/well) containing S17 stromal cells or CD40L fibroblasts in medium containing no added cytokines, IL-4, IL-10, or both cytokines. (A) Cell recovery was determined by trypan blue dye exclusion and expressed as the mean number of viable cells. (B) Cell cycle analysis of CD19+cells removed from the CD40L system. (Left) Dot plot of IgM versus DNA content analyzed by propidium iodide staining. (Right) Histogram illustrating DNA content in the IgM+ (R1) versus the IgM (R2) populations. Numbers indicate the percentage of cells in S/G2/M.

Close Modal

or Create an Account

Close Modal
Close Modal