Figure 5
Figure 5. Autoimmunity and expansion of B1b cells requires Itch−/− T cells.(A) Rag1−/− mice were reconstituted with combinations of bone marrow from WT or Itch−/− mouse strains (Table 1) and analyzed 14 to 18 weeks later. Anti-IgM and anti-IgE ELISA are shown for sera of mixed chimeras. (B) Representative FACS plots of peritoneal cells from mixed chimeric mice are shown for B cells after gating on lymphocytes using side and forward scatter profiles. (C) B1-gated peritoneal cells from the same mice were stained for B1a (Mac1+CD5+) and B1b (Mac1+CD5−) cells. (D) Rag1−/− mice were reconstituted with WT or Itch−/− purified peritoneal B1 cells together with purified Itch−/− or WT CD4+ T cells (LN), as indicated. Sera were analyzed 4 weeks later for total IgM (left) and IgE (right) by ELISA. (*P < .05). (E) Rag1−/− mice were reconstituted with WT or Itch−/− B cells (LN) together with purified Itch−/− or WT CD4+ T cells, as indicated. Sera were analyzed 4 weeks later for IgE by ELISA.

Autoimmunity and expansion of B1b cells requires Itch−/− T cells.(A) Rag1−/− mice were reconstituted with combinations of bone marrow from WT or Itch−/− mouse strains (Table 1) and analyzed 14 to 18 weeks later. Anti-IgM and anti-IgE ELISA are shown for sera of mixed chimeras. (B) Representative FACS plots of peritoneal cells from mixed chimeric mice are shown for B cells after gating on lymphocytes using side and forward scatter profiles. (C) B1-gated peritoneal cells from the same mice were stained for B1a (Mac1+CD5+) and B1b (Mac1+CD5) cells. (D) Rag1−/− mice were reconstituted with WT or Itch−/− purified peritoneal B1 cells together with purified Itch−/− or WT CD4+ T cells (LN), as indicated. Sera were analyzed 4 weeks later for total IgM (left) and IgE (right) by ELISA. (*P < .05). (E) Rag1−/− mice were reconstituted with WT or Itch−/− B cells (LN) together with purified Itch−/− or WT CD4+ T cells, as indicated. Sera were analyzed 4 weeks later for IgE by ELISA.

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