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. 2008 Jun 17;84(3):842–851. doi: 10.1189/jlb.0208087

Fig. 6.

Fig. 6.

Enhanced B cell proliferation and expansion of MZ B cells. (A) B and T cells purified from spleens of WT and GAPT−/− mice were incubated with medium (–), anti-IgM F(ab′)2, anti-CD40, and LPS or anti-CD3 and PMA plus ionomycin (P+I), respectively, for 48 h. Proliferating cells were then examined by measuring [3H] thymidine incorporation. Experiments were performed in triplicate, and figures represent three independent experiments with similar results. Left panel, B cells were stimulated by anti-IgM at 10 μg/ml; right panel, B cells were stimulated by anti-IgM at different concentrations shown in the figure. (B) The absolute numbers of total T cells, B cells, and B cell subsets per mouse spleen. (C) Percentages of MZ B cells in WT and GAPT−/− mice. MZ B cells were characterized as CD23CD21+B220+ cells. Figure also shows the increased percentage of MZ and T2 B cells as a result of increased MZ B cell percentage. (D) Concentrations of circulating serum Ig isotypes in aged GAPT−/− mice. *, P < 0.05; **, P < 0.01.