Charles Hong
Associate Professor of Medicine
Last active: 9/28/2016

Selective modulation of TLR4-activated inflammatory responses by altered iron homeostasis in mice.

Wang L, Harrington L, Trebicka E, Shi HN, Kagan JC, Hong CC, Lin HY, Babitt JL, Cherayil BJ
J Clin Invest. 2009 119 (11): 3322-8

PMID: 19809161 · PMCID: PMC2769199 · DOI:10.1172/JCI39939

Mice deficient in the hemochromatosis gene, Hfe, have attenuated inflammatory responses to Salmonella infection associated with decreased macrophage TNF-alpha and IL-6 biosynthesis after exposure to LPS. In this study, we show that the abnormal cytokine production is related to impaired TLR4 signaling. Despite their abnormal response to LPS, Hfe KO macrophages produced amounts of TNF-alpha similar to those in WT cells after TLR2 stimulation. Consistent with this finding, LPS-induced activation of Mal/MyD88-dependent events was normal in the mutant macrophages. However, LPS-induced IFN-beta expression, a TRAM/TRIF-dependent response activated by TLR4, was reduced by Hfe deficiency. This reduction could be replicated in WT macrophages with the use of iron chelators. In contrast, TLR3-activated expression of IFN-beta, a TRIF-dependent response, was normal in Hfe KO macrophages and was unaffected by iron chelation. Our data suggest that low intracellular iron selectively impairs signaling via the TLR4/TRAM/TRIF pathway proximal to TRIF and results in reduced LPS-induced cytokine expression. Furthermore, by mimicking the altered iron metabolism associated with Hfe deficiency, we found that 3 different inhibitors of hepcidin attenuated Salmonella-induced and noninfectious enterocolitis. Thus, manipulation of iron homeostasis could represent a new therapeutic approach to controlling inflammation.

MeSH Terms (17)

Animals Enterocolitis Gene Expression Regulation Hemochromatosis Homeostasis Immunity, Innate Inflammation Iron Lipopolysaccharides Macrophages Mice Mice, Inbred C57BL Mice, Knockout Myeloid Differentiation Factor 88 Salmonella Infections Signal Transduction Toll-Like Receptor 4

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