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. Author manuscript; available in PMC: 2017 Apr 19.
Published in final edited form as: Immunity. 2016 Mar 2;44(4):769–781. doi: 10.1016/j.immuni.2016.01.011

Figure 2. Antigen-specific B lineage cells and positive selection for the bone marrow plasma cell fate.

Figure 2

(A) PE-binding among Dump-B220+ cells in naïve and immunized Aicdacre/− Igh96K/+ R26LSL-YFP mice following column-based cell enrichment. (B) GC and memory cells among antigen-specific B cells gated in (A) and identified based on surface expression of CD38 and GL7. (C) Expression history of Aicda among antigen-specific naïve B cells and GC and memory B cells, gated as in (A–B). (D) IgM and IgG1 surface expression in indicated antigen-specific populations, gated as shown in (A–C). (E) Plasma cells were enriched in immunized mice from the bone marrow based on CD138 surface expression and assessed for intracellular antigen-binding and isotype expression. BMPCs were further gated as DumpYFP+. (F) Fraction of IgG1+ cells among YFP+ cells in the antigen-specific memory, GC, and BMPC compartments of Aicdacre/− Igh96K/+ R26LSL-YFP mice 40–59 days after immunization with PE. Results are combined from 3 independent experiments; each line connects the indicated cell populations from the same animal. **** p <0.0001, ** p = 0.009. Two-tailed Mann-Whitney test was used to assess significance. See also Figure S1.