Table 1.

Expansion of bone marrow pro–B cells in 4 independently derived mouse lines bearing an Eμ-A1 transgene

LineNIgM+BPre-BPro-BPre-B/Pro-B
%Cells (× 10−6)%Cells (× 10−6)%Cells (× 10−6)
Wild-type 47 ± 2.0 2.0 ± 0.93 46 ± 13 2.5 ± 0.15 6.7 ± 2.4 0.41 ± 0.21 7.4 
41 ± 8 1.5 ± 0.61 34 ± 10 1.3 ± 0.57 25 ± 3.4 0.94 ± 0.44 1.4 
39 ND 42 ND 19 ND 2.3 
14 58 ND 28  ND 10 ND 2.8 
95 40 ± 5.3 ND 47  ± 7.2 ND 9.8 ± 3.1 ND 5.5 
LineNIgM+BPre-BPro-BPre-B/Pro-B
%Cells (× 10−6)%Cells (× 10−6)%Cells (× 10−6)
Wild-type 47 ± 2.0 2.0 ± 0.93 46 ± 13 2.5 ± 0.15 6.7 ± 2.4 0.41 ± 0.21 7.4 
41 ± 8 1.5 ± 0.61 34 ± 10 1.3 ± 0.57 25 ± 3.4 0.94 ± 0.44 1.4 
39 ND 42 ND 19 ND 2.3 
14 58 ND 28  ND 10 ND 2.8 
95 40 ± 5.3 ND 47  ± 7.2 ND 9.8 ± 3.1 ND 5.5 

Bone marrow cells from mice 4 to 8 weeks of age were analyzed using 3-color flow cytometry for the expression of B220, IgM, and CD43. Populations were expressed as a percentage of B220+ cells, including IgM+ B cells, IgMCD43pre–B cells, and IgM-CD43+ pro–B cells. In WT and line 8 mice, absolute cell numbers contained in 2 femurs are also given. Ratios of pre– to pro–B cells are also given. Mean ± SD are given for the indicated number of mice analyzed, except for lines 6 and 14, in which only 2 mice were studied. ND indicates not done.

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