Figure 2
Macrophage Lcn2 production and antibacterial activity. Macrophages were harvested from WT and Hfe−/− mice and treated with 100 U/mL IFN-γ or infected with WT S Typhimurium (S Tm) for 24 hours. The production of Lcn2 was investigated in culture supernatants by ELISA (A). Data were log-transformed and compared by ANOVA and are shown as mean ± SEM of at least 3 independent experiments. WT, Hfe+/−, and Hfe−/− mice were infected with WT Salmonella. The bacterial burden was determined by gentamicin protection assay (B). In parallel experiments, the acquisition of 59Fe by intramacrophage Salmonella was determined (C). In additional experiments, the survival of S Typhimurium within C57BL/6 WT, Hfe−/−, Lcn2−/−, and Hfe−/−Lcn2−/− macrophages (D) as well as bacterial iron uptake within these cells (E) were determined. These data were analyzed by ANOVA and shown as mean ± SEM of at least 3 independent experiments. *P < .05 compared with the solvent-treated control of the corresponding genotype, #P < .05 for the comparison of cells of different genotype subjected to the same stimulatory regimen.

Macrophage Lcn2 production and antibacterial activity. Macrophages were harvested from WT and Hfe−/− mice and treated with 100 U/mL IFN-γ or infected with WT S Typhimurium (S Tm) for 24 hours. The production of Lcn2 was investigated in culture supernatants by ELISA (A). Data were log-transformed and compared by ANOVA and are shown as mean ± SEM of at least 3 independent experiments. WT, Hfe+/−, and Hfe−/− mice were infected with WT Salmonella. The bacterial burden was determined by gentamicin protection assay (B). In parallel experiments, the acquisition of 59Fe by intramacrophage Salmonella was determined (C). In additional experiments, the survival of S Typhimurium within C57BL/6 WT, Hfe−/−, Lcn2−/−, and Hfe−/−Lcn2−/− macrophages (D) as well as bacterial iron uptake within these cells (E) were determined. These data were analyzed by ANOVA and shown as mean ± SEM of at least 3 independent experiments. *P < .05 compared with the solvent-treated control of the corresponding genotype, #P < .05 for the comparison of cells of different genotype subjected to the same stimulatory regimen.

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