The American journal of physiology · 1999
Iron primes hepatic macrophages for NF-kappaB activation in alcoholic liver injury.
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Tsukamoto H, Lin M, Ohata M, Giulivi C, French S W, Brittenham G
Аннотация
NF-kappaB activation induced by lipopolysaccharide (LPS) in cultured hepatic macrophages (HM) may be abrogated by pretreatment of cells with a lipophilic iron chelator, 1,2-dimethyl-3-hydroxypyrid-4-one (L1, deferiprone), suggesting a role for iron in this molecular event [M. Lin, M., R. A. Rippe, O. Niemelä, G. Brittenham, and H. Tsukamoto, Am. J. Physiol. 272 (Gastrointest. Liver Physiol. 35): G1355-G1364, 1997]. To ascertain the relevance in vivo of this hypothesis, HM from an experimental model of alcoholic liver injury were examined for the relationship between nuclear factor (NF)-kappaB activation and iron storage. HM showed a significant increase in nonheme iron concentration (+70%), accompanied by enhanced generation of electron paramagnetic resonance-detected radicals (+200%), NF-kappaB activation (+100%), and tumor necrosis factor-alpha (+150%) and macrophage inflammatory protein-1 (+280%) mRNA induction. Treatment of the cells ex vivo with L1 normalized all these parameters. HM content of ferritin protein, ferritin L chain mRNA, and hemeoxygenase-1 mRNA and splenic content of nonheme iron were increased, suggesting enhanced heme turnover as a cause of the increased iron storage and NF-kappaB activation. To test this possibility, increased iron content in HM was reproduced in vitro by phagocytosis of heat-treated red blood cells. Treatment caused a 40% increase in nonheme iron concentration and accentuated LPS-induced NF-kappaB activation twofold. Both effects could be abolished by pretreatment of cells with zinc protoporphyrin, a hemeoxygenase inhibitor. To extend this observation, animals were splenectomized before 9-wk alcohol feeding. Splenectomy resulted in further increments in HM nonheme iron storage (+60%) and NF-kappaB activation (+90%) and mononuclear cell infiltration (+450%), particularly around the iron-loaded HM in alcohol-fed animals. These results support the pivotal role of heme-derived iron in priming HM for NF-kappaB activation and expression of proinflammatory genes in alcoholic liver injury.
Предметные рубрики MeSH
AnimalsApoferritinsCalcium-Binding ProteinsCentral Nervous System DepressantsChemokine CCL4Disease Models, AnimalErythrocytesEthanolFerritinsGene ExpressionHeme Oxygenase (Decyclizing)Hepatitis, AlcoholicIronKupffer CellsLeukocyte L1 Antigen ComplexLipopolysaccharidesLiverMacrophage Inflammatory ProteinsMaleMembrane GlycoproteinsNF-kappa BNeural Cell Adhesion MoleculesPhagocytosisPicolinesProto-Oncogene ProteinsRNA, MessengerRatsRats, WistarSplenectomyTumor Necrosis Factor-alphaWnt2 Protein