Figure 2
Figure 2. Preleukemic Eμ-myc/bcl-2−/− reconstituted mice have abnormally low numbers of mature B cells. Spleen and LNs were harvested from lethally irradiated wt mice 8 to 12 weeks after reconstitution with fetal liver cells from wt, bcl-2−/−, Eμ-myc, and Eμ-myc/bcl-2−/− (E14.5) embryos. Single-cell suspensions were prepared, stained with fluorochrome-conjugated monoclonal antibodies to B220, IgM, IgD, and Ly5.2, and analyzed by FACS. (A) Representative FACS profiles illustrating the abundance of immature (R1: B220+ sIgMhi sIgDlo) and mature (R2: B220+ sIgMlo sIgDhi) splenic B cells, and total numbers in spleens from wt, bcl-2−/−, Eμ-myc/bcl-2+/+, and Eμ-myc/bcl-2−/− fetal liver reconstituted mice. Profiles are gated on Ly5.2+ B220+ cells. (B) Total numbers of donor-derived mature B cells (B220+ sIgMlo sIgDhi) in LNs from wt, bcl-2−/−, Eμ-myc, and Eμ-myc/bcl-2−/− reconstituted mice. Graphs represent means ± SEM from 5 to 8 mice of each genotype. Statistically significant differences: *P < .05; **P < .001.

Preleukemic Eμ-myc/bcl-2−/− reconstituted mice have abnormally low numbers of mature B cells. Spleen and LNs were harvested from lethally irradiated wt mice 8 to 12 weeks after reconstitution with fetal liver cells from wt, bcl-2−/−, Eμ-myc, and Eμ-myc/bcl-2−/− (E14.5) embryos. Single-cell suspensions were prepared, stained with fluorochrome-conjugated monoclonal antibodies to B220, IgM, IgD, and Ly5.2, and analyzed by FACS. (A) Representative FACS profiles illustrating the abundance of immature (R1: B220+ sIgMhi sIgDlo) and mature (R2: B220+ sIgMlo sIgDhi) splenic B cells, and total numbers in spleens from wt, bcl-2−/−, Eμ-myc/bcl-2+/+, and Eμ-myc/bcl-2−/− fetal liver reconstituted mice. Profiles are gated on Ly5.2+ B220+ cells. (B) Total numbers of donor-derived mature B cells (B220+ sIgMlo sIgDhi) in LNs from wt, bcl-2−/−, Eμ-myc, and Eμ-myc/bcl-2−/− reconstituted mice. Graphs represent means ± SEM from 5 to 8 mice of each genotype. Statistically significant differences: *P < .05; **P < .001.

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