Figure 5. Iron chelation suppresses the induction of FPN1 after erythrophagocytosis by J774 macrophages. J774 cells (approximately 1 × 106) were incubated in the presence (+) or absence (-) of 15 × 106 opsonized human erythrocytes (EIgG) for 1.5 hours. Noningested erythrocytes were lysed and removed, SIH was added at the indicated concentrations, and incubation was continued for 6 hours. (A) Northern analysis of FPN1. (B) Western blot analysis of FPN1. (C) FPN1 mRNA levels normalized to β-actin (♦), and protein levels of the 65-kDa FPN1 band (▪) plotted as a function of SIH concentration. A third independent experiment, in which FPN1 protein (but not mRNA) was measured, yielded similar results.
Figure 5.

Iron chelation suppresses the induction of FPN1 after erythrophagocytosis by J774 macrophages. J774 cells (approximately 1 × 106) were incubated in the presence (+) or absence (-) of 15 × 106 opsonized human erythrocytes (EIgG) for 1.5 hours. Noningested erythrocytes were lysed and removed, SIH was added at the indicated concentrations, and incubation was continued for 6 hours. (A) Northern analysis of FPN1. (B) Western blot analysis of FPN1. (C) FPN1 mRNA levels normalized to β-actin (♦), and protein levels of the 65-kDa FPN1 band (▪) plotted as a function of SIH concentration. A third independent experiment, in which FPN1 protein (but not mRNA) was measured, yielded similar results.

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