Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/110349
Author(s): Silva-Gomes, S
Santos, AG
Caldas, C
Silva, CM
Neves, JV
Lopes, J
Carneiro, F
Rodrigues, PN
Duarte, TL
Title: Transcription factor NRF2 protects mice against dietary iron-induced liver injury by preventing hepatocytic cell death
Publisher: Elsevier
Issue Date: 2014
Abstract: BACKGROUND & AIMS: The liver, being the major site of iron storage, is particularly exposed to the toxic effects of iron. Transcription factor NRF2 is critical for protecting the liver against disease by activating the transcription of genes encoding detoxification/antioxidant enzymes. We aimed to determine if the NRF2 pathway plays a significant role in the protection against hepatic iron overload.METHODS: Wild-type and Nrf2(-/-) mouse primary hepatocytes were incubated with ferric ammonium citrate. Wild-type and Nrf2(-/-) mice were fed standard rodent chow or iron-rich diet for 2weeks, with or without daily injection of the antioxidant mito-TEMPOL.RESULTS: In mouse hepatocytes, iron induced the nuclear translocation of NRF2 and the expression of cytoprotective genes in an NRF2-dependent manner. Moreover, Nrf2(-/-) hepatocytes were highly susceptible to iron-induced cell death. Wild-type and Nrf2(-/-) mice fed iron-rich diet accumulated similar amounts of iron in the liver and were equally able to increase the expression of hepatic hepcidin and ferritin. Nevertheless, in Nrf2-null mice the iron loading resulted in progressive liver injury, ranging from mild confluent necrosis to severe necroinflammatory lesions. Hepatocytic cell death was associated with gross ultrastructural damage to the mitochondria. Notably, liver injury was prevented in iron-fed animals that received mito-TEMPOL.CONCLUSIONS: NRF2 protects the mouse liver against the toxicity of dietary iron overload by preventing hepatocytic cell death. We identify NRF2 as a potential modifier of liver disease in iron overload pathology and show the beneficial effect of the antioxidant mito-TEMPOL in a mouse model of dietary iron-induced liver injury.
Subject: Animals
Antioxidants/pharmacology
Cyclic N-Oxides/pharmacology
Disease Models, Animal
Hepatocytes/drug effects
Hepatocytes/metabolism
Hepatocytes/pathology
Iron Overload/drugtherapy
Iron Overload/metabolism
Iron Overload/pathology
Iron Dietary/toxicity
Liver/injuries
Liver/metabolism
Liver/pathology
Male
Mice
Mice Inbred C57BL
Mice Knockout
Mitochondria Liver/drug effects
Mitochondria Liver/metabolism
NF-E2-Related Factor 2/deficiency
NF-E2-Related Factor 2/genetics
NF-E2-Related Factor 2/metabolism
Spin Labels
URI: http://hdl.handle.net/10216/110349
Source: Journal of Hepatology, vol. 60(2), p. 354-61
Related Information: info:eu-repo/grantAgreement/FCT/5876-PPCDTI/101177/PT
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
Appears in Collections:I3S - Artigo em Revista Científica Internacional

Files in This Item:
File Description SizeFormat 
SilvaGomes2014i3S.pdf786.05 kBAdobe PDFThumbnail
View/Open
Silva-Gomes2014_SupMat1.pdf1.65 MBAdobe PDFThumbnail
View/Open
Silva-Gomes2014_SupMat2.pdf735.23 kBAdobe PDFThumbnail
View/Open
Silva-Gomes2014_SupMat3.pdf646.36 kBAdobe PDFThumbnail
View/Open
Silva-Gomes2014_SupMat4.pdf376.46 kBAdobe PDFThumbnail
View/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.