TY - JOUR T1 - Interferon-gamma limits the availability of iron for intramacrophage Salmonella typhimurium. JF - Eur J Immunol Y1 - 2008 A1 - Nairz, Manfred A1 - Fritsche, Gernot A1 - Peter Brunner A1 - Talasz, Heribert A1 - Hantke, Klaus A1 - Weiss, Günter KW - Acute-Phase Proteins KW - Animals KW - Antimicrobial Cationic Peptides KW - Cation Transport Proteins KW - Cell Line KW - Ferritins KW - Heme Oxygenase (Decyclizing) KW - Hepcidins KW - Interferon-gamma KW - Iron KW - Lipocalins KW - Macrophages KW - Mice KW - Nitric Oxide KW - Oncogene Proteins KW - Salmonella typhimurium KW - Transferrin KW - Tumor Necrosis Factor-alpha AB -

In stimulating effector functions of mononuclear phagocytes, IFN-gamma is of pivotal importance in host defense against intramacrophage pathogens including salmonellae. As the activity of IFN-gamma is modulated by iron and since a sufficient availability of iron is essential for the growth of pathogens, we investigated the regulatory effects of IFN-gamma on iron homeostasis and immune function in murine macrophages infected with Salmonella typhimurium. In Salmonella-infected phagocytes, IFN-gamma caused a significant reduction of iron uptake via transferrin receptor 1 and resulted in an increased iron efflux caused by an enhanced expression of the iron exporter ferroportin 1. Moreover, the expression of haem oxygenase 1 and of the siderophore-capturing antimicrobial peptide lipocalin 2 was markedly elevated following bacterial invasion, with IFN-gamma exerting a super-inducing effect. This observed regulatory impact of IFN-gamma reduced the intracellular iron pools within infected phagocytes, thus restricting the acquisition of iron by engulfed Salmonella typhimurium while concomitantly promoting NO and TNF-alpha production. Our data suggest that the modulation of crucial pathways of macrophage iron metabolism in response to IFN-gamma concordantly aims at withdrawing iron from intracellular Salmonella and at strengthening macrophage immune response functions. These regulations are thus consistent with the principles of nutritional immunity.

VL - 38 UR - http://www.ncbi.nlm.nih.gov/pubmed/18581323 IS - 7 ER -