Fig. 6: Normal germinal center (GC) B, memory B, and plasma cell formation in iB-μMT mice. | Cellular & Molecular Immunology

Fig. 6: Normal germinal center (GC) B, memory B, and plasma cell formation in iB-μMT mice.

From: Regeneration of immunocompetent B lymphopoiesis from pluripotent stem cells guided by transcription factors

Fig. 6

A Plasma cells and antigen-specific GC B cells in the spleens of iB-μMT mice. Spleen cells were isolated from B6 and iB-μMT mice 14 days after primary intraperitoneal immunization with 100 μg NP-CGG in alum. Plasma cells (LinB220low/−CD138+) and antigen-specific GC B cells (LinB220+CD138NP+GL7+CD38) were analyzed by flow cytometry. Data from one representative B6 mouse and two representative iB-μMT mice are shown. Lin was defined as Ter119Mac1Gr1NK1.1CD3CD4CD8. B Antigen-specific class-switched IgG1+ memory B cells in the spleens of iB-μMT mice. Spleen cells were isolated from B6 and iB-μMT mice 21 days after primary intraperitoneal immunization with 100 μg NP-CGG in alum. Representative flow cytometry plots of antigen-specific class-switched IgG1+ memory B cells (LinIgDIgMCD138B220+NP+CD38+IgG1+) from one B6 mouse and two iB-μMT mice are shown. Lin was defined as Ter119Mac1Gr1NK1.1CD3CD4CD8. C, D Long-lived plasma cells in the bone marrow of iB-μMT mice. Long-lived plasma cells (LinIgMCD138+CD22CD19MHCII) in the bone marrow of B6 and iB-μMT mice were analyzed by flow cytometry. Representative plots from B6 and iB-μMT mice 21 days after priming with NP-CGG in alum (C) and 17 days after NP-CGG boost (D) are shown. Lin- was defined as Ter119Mac1Gr1NK1.1CD3CD4CD8

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