Figure 5
Figure 5. Pre-neoplastic Eμ-myc/Suz12Plt8/+ mice have an expanded B-lymphoid compartment. (A) Automated enumeration of peripheral blood leukocytes from preneoplastic Eμ-myc (n = 17), Eμ-myc/Bmi1+/− (n = 8), and Eμ-myc/Suz12Plt8/+ (n = 12) mice. Immunophenotypic characterization of B-lymphocyte subsets from the (B) peripheral blood, (C) bone marrow, and (D) spleen of preneoplastic Eμ-myc, Eμ-myc/Bmi1+/−, and Eμ-myc/Suz12Plt8/+ mice. Data represent mean ± standard deviation. One-way analysis of variance followed by Tukey’s post hoc test was used for pairwise comparisons (*P < .05; **P < .01; ***P < .001). Cell surface markers used to define B-cell subsets are as follows: BM pro-B, B220+CD19+c-Kit+IgM−IgD−; BM pre-B-II, B220+CD19+c-Kit−CD25+IgM−IgD−; BM pro + pre-B, blood sIg− B, or spleen pre-B, B220+CD19+cKit−IgM−IgD−; spleen immature B, B220+CD19+c-Kit−IgM+IgD−, BM sIg+; spleen mature B, B220+CD19+c-Kit−IgM+IgD+.

Pre-neoplastic Eμ-myc/Suz12Plt8/+ mice have an expanded B-lymphoid compartment. (A) Automated enumeration of peripheral blood leukocytes from preneoplastic Eμ-myc (n = 17), Eμ-myc/Bmi1+/− (n = 8), and Eμ-myc/Suz12Plt8/+ (n = 12) mice. Immunophenotypic characterization of B-lymphocyte subsets from the (B) peripheral blood, (C) bone marrow, and (D) spleen of preneoplastic Eμ-myc, Eμ-myc/Bmi1+/−, and Eμ-myc/Suz12Plt8/+ mice. Data represent mean ± standard deviation. One-way analysis of variance followed by Tukey’s post hoc test was used for pairwise comparisons (*P < .05; **P < .01; ***P < .001). Cell surface markers used to define B-cell subsets are as follows: BM pro-B, B220+CD19+c-Kit+IgMIgD; BM pre-B-II, B220+CD19+c-KitCD25+IgMIgD; BM pro + pre-B, blood sIg B, or spleen pre-B, B220+CD19+cKitIgMIgD; spleen immature B, B220+CD19+c-KitIgM+IgD, BM sIg+; spleen mature B, B220+CD19+c-KitIgM+IgD+.

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