Figure 4.
Figure 4. miR-17-92 regulates B-cell differentiation and function in cGVHD. B6 to BALB/c murine model of cGVHD was set up as described in Figure 1. Sixty days after BMT, data from 1 representative mouse of each group (A) and mean percentage of GL-7+Fas+ GC B cells on gated H2Kb+B220+ cells, and B220−CD138+ plasma cells on gated H2Kb+ cells are shown in spleen (B). (C) Sera from whole blood were taken for enzyme-linked immunosorbent assay (ELISA) measuring anti-dsDNA IgG and IgG2c autoantibodies as described in “Materials and methods.” (D) Mean fluorescence intensity (MFI) of MHC-II (IAb) and CD86 expression are shown on gated H2Kb+B220+ in spleen (N = 4-5 mice per group shown). Data shown are the representative of 3 individual experiments with a cumulative total of 15 to 20 mice per group. (E) Serum IL-10 levels in recipients were measured using the CBA kit 60 days post-BMT (N = 4-5 mice per group shown). *P < .05; **P < .01; ***P < .001.

miR-17-92 regulates B-cell differentiation and function in cGVHD. B6 to BALB/c murine model of cGVHD was set up as described in Figure 1. Sixty days after BMT, data from 1 representative mouse of each group (A) and mean percentage of GL-7+Fas+ GC B cells on gated H2Kb+B220+ cells, and B220CD138+ plasma cells on gated H2Kb+ cells are shown in spleen (B). (C) Sera from whole blood were taken for enzyme-linked immunosorbent assay (ELISA) measuring anti-dsDNA IgG and IgG2c autoantibodies as described in “Materials and methods.” (D) Mean fluorescence intensity (MFI) of MHC-II (IAb) and CD86 expression are shown on gated H2Kb+B220+ in spleen (N = 4-5 mice per group shown). Data shown are the representative of 3 individual experiments with a cumulative total of 15 to 20 mice per group. (E) Serum IL-10 levels in recipients were measured using the CBA kit 60 days post-BMT (N = 4-5 mice per group shown). *P < .05; **P < .01; ***P < .001.

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