Figure 5
Postresolution Mφs trigger FoxP3 expression in CD4 T cells. (A) The relative ratios of blood vs peritoneal Tregs was determined 9 days after zymosan injection (0.1 mg) with postresolution resM, moMφs, and moDCs incubated with CD4 T- and Trp-1 peptide (SGHNCGTCRPGWRGAACNQKILTVR) + TGF-β for 5 days and analyzed for the presence of (B) Foxp3 expression and effector T-cell proliferation. Analysis of these Mφ/DC populations revealed a (C) migratory phenotype that was (D) confirmed by injecting PKH26-PCLgreen into mice on day 6 post-zymosan (0.1 mg), which also had PKH26-PCLred injected into their naïve peritoneum to label resMφs. This resulted in infiltrating moMφs and moDCs labeling positively for only PKH26-PCLgreen (shown), whereas resMφs were labeled with both PKH26-PCLred and PKH26-PCLgreen (not shown). Data are presented as mean ± SEM for n = 6 mice/group.

Postresolution Mφs trigger FoxP3 expression in CD4 T cells. (A) The relative ratios of blood vs peritoneal Tregs was determined 9 days after zymosan injection (0.1 mg) with postresolution resM, moMφs, and moDCs incubated with CD4 T- and Trp-1 peptide (SGHNCGTCRPGWRGAACNQKILTVR) + TGF-β for 5 days and analyzed for the presence of (B) Foxp3 expression and effector T-cell proliferation. Analysis of these Mφ/DC populations revealed a (C) migratory phenotype that was (D) confirmed by injecting PKH26-PCLgreen into mice on day 6 post-zymosan (0.1 mg), which also had PKH26-PCLred injected into their naïve peritoneum to label resMφs. This resulted in infiltrating moMφs and moDCs labeling positively for only PKH26-PCLgreen (shown), whereas resMφs were labeled with both PKH26-PCLred and PKH26-PCLgreen (not shown). Data are presented as mean ± SEM for n = 6 mice/group.

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