Figure 6
Figure 6. Induction of IgG-producing plasma cells from CD27+ B cells and IgM-producing plasma cells from CD27− B cells. (A,C) Intracytoplasmic immunoglobulin staining was used to assess immunoglobulin production with each phase. Intracellular IgM increased in both (A) CD27+ and (C) CD27− B cells by the end of phase II, and then declined after phase III. In contrast, CD27+ cells had a steady increase in intracellular IgG staining through terminal differentiation into CD138+ plasma cells. Figures are representative of 4 independent experiments with cells from 4 different blood donors. (B,D) IgG, IgM, and IgA were measured by ELISA from supernatants taken at the end of each culture phase for (B) CD27+ and (D) CD27− B cells. Error bars are mean ± standard error for all plots. Experimental data are from 5 separate experiments each with different blood donors.

Induction of IgG-producing plasma cells from CD27+ B cells and IgM-producing plasma cells from CD27 B cells. (A,C) Intracytoplasmic immunoglobulin staining was used to assess immunoglobulin production with each phase. Intracellular IgM increased in both (A) CD27+ and (C) CD27 B cells by the end of phase II, and then declined after phase III. In contrast, CD27+ cells had a steady increase in intracellular IgG staining through terminal differentiation into CD138+ plasma cells. Figures are representative of 4 independent experiments with cells from 4 different blood donors. (B,D) IgG, IgM, and IgA were measured by ELISA from supernatants taken at the end of each culture phase for (B) CD27+ and (D) CD27 B cells. Error bars are mean ± standard error for all plots. Experimental data are from 5 separate experiments each with different blood donors.

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