Figure 3
Figure 3. Bim-deficient mice accumulated abnormally increased numbers of memory B cells. Wild-type and bim−/− mice were immunized with NP. Spleen cells were harvested after 7, 14, and 28 days and analyzed for their content of IgM−IgD−Gr-1−Mac-1−B220+IgG1+NP+ B cells by flow cytometry (as in Figure 1A). Within this cell population, cells with a memory phenotype (CD38high) and GC phenotype (CD38low) were quantified by FACS analysis (as in Figure 1A). The total numbers of memory B cells in the spleen (A; *P < .05), percentages of memory B cells in the blood (B), total numbers of GC B cells in the spleen (C; *P ≤ .05) and the percentages of GC B cells in the blood (D) are indicated. Data represent the mean (± SD) of n = 4 to 8 mice.

Bim-deficient mice accumulated abnormally increased numbers of memory B cells. Wild-type and bim−/− mice were immunized with NP. Spleen cells were harvested after 7, 14, and 28 days and analyzed for their content of IgMIgDGr-1Mac-1B220+IgG1+NP+ B cells by flow cytometry (as in Figure 1A). Within this cell population, cells with a memory phenotype (CD38high) and GC phenotype (CD38low) were quantified by FACS analysis (as in Figure 1A). The total numbers of memory B cells in the spleen (A; *P < .05), percentages of memory B cells in the blood (B), total numbers of GC B cells in the spleen (C; *P ≤ .05) and the percentages of GC B cells in the blood (D) are indicated. Data represent the mean (± SD) of n = 4 to 8 mice.

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