Figure 6.
Figure 6. Endogenous BM B cells from Rag2°IL2Rβ° and Flt3IL7Rα° mice and B cells generated after reconstitution of these recipient mice. (A) CD19 versus NK1.1 profile of the bone marrow cells of the different recipient mice. Shown are CD3-negative bone marrow lymphocytes. Note that the CD19+ in the C57Bl/6 mouse contain Ig– precursor (pro– and pre–B cells) as well as Ig+ immature and mature B cells, while in the Rag2°IL2Rβ° mouse CD19+ cells only comprise pro–B cells, as B-cell development is arrested at the transition of the pro– to pre–B-cell stage (according to Hardy et al17) due to the Rag2-mutation. Absolute cell numbers for CD19+ and NK1.1+CD3– cells are given. (B) CD19 versus CD25 profiles. Phenotype of the bone marrow B cells from reconstituted Rag°IL2Rβ° and Flt3IL7Rα° mice, then weeks after transplantation with 1 × 104 sorted Lin–cKit+Sca1+ cells from wild-type C57Bl/6Ly5.1 mice. Age-matched C57Bl/6Ly5.1 mice were used for control. (C) Profiles of CD19 versus IgM. Shown are CD45.1+PI– cells falling in a lymphocyte gate. One representative analysis of at least 3 experiments is shown. Numbers indicate the absolute cell number in the respective quadrant. The dotted line separates the flow cytometric results from the unmanipulated C57Bl/6Ly5.1 from that of the reconstituted recipient mice.

Endogenous BM B cells from Rag2°IL2Rβ° and Flt3IL7Rα° mice and B cells generated after reconstitution of these recipient mice. (A) CD19 versus NK1.1 profile of the bone marrow cells of the different recipient mice. Shown are CD3-negative bone marrow lymphocytes. Note that the CD19+ in the C57Bl/6 mouse contain Ig precursor (pro– and pre–B cells) as well as Ig+ immature and mature B cells, while in the Rag2°IL2Rβ° mouse CD19+ cells only comprise pro–B cells, as B-cell development is arrested at the transition of the pro– to pre–B-cell stage (according to Hardy et al17 ) due to the Rag2-mutation. Absolute cell numbers for CD19+ and NK1.1+CD3 cells are given. (B) CD19 versus CD25 profiles. Phenotype of the bone marrow B cells from reconstituted Rag°IL2Rβ° and Flt3IL7Rα° mice, then weeks after transplantation with 1 × 104 sorted LincKit+Sca1+ cells from wild-type C57Bl/6Ly5.1 mice. Age-matched C57Bl/6Ly5.1 mice were used for control. (C) Profiles of CD19 versus IgM. Shown are CD45.1+PI cells falling in a lymphocyte gate. One representative analysis of at least 3 experiments is shown. Numbers indicate the absolute cell number in the respective quadrant. The dotted line separates the flow cytometric results from the unmanipulated C57Bl/6Ly5.1 from that of the reconstituted recipient mice.

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