Figure 2
Figure 2. Bad- or Bid-deficiency did not further enhance the abnormal accumulation of antigen-specific B cells in bim−/− mice. Mice (wt, bim−/−, bim−/−bad−/−, or bim−/−bid−/−) were injected intraperitoneally with 100 μg of NP coupled to KLH, and leukocytes were collected from the spleen after 7, 14, and 28 days. Cells were stained with fluorochrome-conjugated surface marker-specific monoclonal antibodies and gated on IgM−IgD−Gr-1−Mac-1− cells by flow cytometry and analyzed for their proportion of antigen-specific B220+IgG1+NP+ B cells as illustrated in Figure 1A. The total numbers of antigen-specific IgG1+NP+ B cells in the spleen of bim−/−bad−/− and bim−/−bid−/− (A) were determined, and their percentages in the peripheral blood are also shown (B). Each data point represents a mouse: n = 2-3 bim−/−bad−/− mice, n = 2 bim−/−bid−/− mice, n = 3 bim−/−, and n = 3 wt mice.

Bad- or Bid-deficiency did not further enhance the abnormal accumulation of antigen-specific B cells in bim−/− mice. Mice (wt, bim−/−, bim−/−bad−/−, or bim−/−bid−/−) were injected intraperitoneally with 100 μg of NP coupled to KLH, and leukocytes were collected from the spleen after 7, 14, and 28 days. Cells were stained with fluorochrome-conjugated surface marker-specific monoclonal antibodies and gated on IgMIgDGr-1Mac-1 cells by flow cytometry and analyzed for their proportion of antigen-specific B220+IgG1+NP+ B cells as illustrated in Figure 1A. The total numbers of antigen-specific IgG1+NP+ B cells in the spleen of bim−/−bad−/− and bim−/−bid−/− (A) were determined, and their percentages in the peripheral blood are also shown (B). Each data point represents a mouse: n = 2-3 bim−/−bad−/− mice, n = 2 bim−/−bid−/− mice, n = 3 bim−/−, and n = 3 wt mice.

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