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. 2017 Jun 23;7:4111. doi: 10.1038/s41598-017-04438-6

Figure 2.

Figure 2

AngII infusion promotes regulatory B cells in B cell replenished Apoe −/− /Baffr −/−mice. (a) Representative dot plots and quantitative analysis of flow cytometry staining of splenic B cell populations. Marginal zone (MZ) B cells are defined as CD21hiCD23 population and follicular B cells (FO) are defined as CD21+CD23+ population amongst B220+ cells. Adoptive transfer of Apoe −/− /Baffr −/− mice with B cells without (left) or with (right) AngII demonstrates replenishment of all B cell subsets. n = 6–8 mice per group. ***p < 0.001. (b) Representative dot plots and quantitative analysis of facs staining of splenic regulatory CD1dhiCD5+ B cells gated on B220+ cells in Apoe −/− /Baffr −/− mice with or without adoptive B cell transfer, infused with PBS for 28 days (left) and their age matched controls with AngII infusion (right). (c) Representative FACS examples and quantitative analysis of splenic CD44hi cells amongst CD4+ T cells in Apoe −/− /Baffr −/− mice with or without adoptive B cell transfer, infused with PBS for 28 days (left) and their age matched controls with AngII infusion (right). (d) Representative examples and quantitative analysis of splenic IFN-γ+ cells amongst CD4+ T cells by intracellular facs staining in Apoe −/− /Baffr −/− mice with or without adoptive B cell transfer, infused with PBS for 28 days (left) and their age matched controls with AngII infusion (right). n = 6–8 mice per group. *p < 0.05, **p < 0.01, ***p < 0.001, ns denotes non significance.

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