Cited by 245Iron Metabolism and DisordersTrace Elements in HealthGenomics and Chromatin Dynamics

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C/EBPα Regulates Hepatic Transcription of Hepcidin, an Antimicrobial Peptide and Regulator of Iron Metabolism

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Courselaud, Brice, Pigeon, Christelle, Inoue, Yusuke, Inoue, Junko, Gonzalez, Frank J., Leroyer, Patricia, Gilot, David, Boudjema, Karim, Guguen-Guillouzo, Christiane, Brissot, Pierre, Loréal, Olivier, Ilyin, Gennady·2002·Journal of Biological Chemistry

DOI 10.1074/jbc.m202653200

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Abstract

Originally identified as a gene up-regulated by iron overload in mouse liver, the HEPC gene encodes hepcidin, the first mammalian liver-specific antimicrobial peptide and potential key regulator of iron metabolism. Here we demonstrate that during rat liver development, amounts of HEPC transcripts were very low in fetal liver, strongly and transiently increased shortly after birth, and reappeared in adult liver. To gain insight into mechanisms that regulate hepatic expression of hepcidin, 5'-flanking regions of human and mouse HEPC genes were isolated and analyzed by functional and DNA binding assays. Human and mouse HEPC promoter-luciferase reporter vectors exhibited strong basal activity in hepatoma HuH-7 and mouse hepatocytes, respectively, but not in non-hepatic U-2OS cells. We found that CCAAT/enhancer-binding protein alpha (C/EBPalpha) and C/EBPbeta were respectively very potent and weak activators of both human and mouse promoters. In contrast, co-expression of hepatocyte nuclear factor 4alpha (HNF4alpha) failed to induce HEPC promoter activity. By electrophoretic mobility shift assay we demonstrated that one putative C/EBP element found in the human HEPC promoter (-250/-230) predominantly bound C/EBPalpha from rat liver nuclear extracts. Hepatic deletion of the C/EBPalpha gene resulted in reduced expression of HEPC transcripts in mouse liver. In contrast, amounts of HEPC transcripts increased in liver-specific HNF4alpha-null mice. Decrease of hepcidin mRNA in mice lacking hepatic C/EBPalpha was accompanied by iron accumulation in periportal hepatocytes. Finally, iron overload led to a significant increase of C/EBPalpha protein and HEPC transcripts in mouse liver. Taken together, these data demonstrate that C/EBPalpha is likely to be a key regulator of HEPC gene transcription and provide a novel mechanism for cross-talk between the C/EBP pathway and iron metabolism.

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Authors: Courselaud, B., Pigeon, C., Inoue, Y., Inoue, J., Gonzalez, F. J., Leroyer, P., Gilot, D., Boudjema, K., Guguen-Guillouzo, C., Brissot, P., Loréal, O., & Ilyin, G.
Affiliations: Inserm (FR)
National Institutes of Health (US)
Corresponding author: Ilyin, Gennady
ORCID: Gonzalez, Frank J.
Gilot, David
Brissot, Pierre
Loréal, Olivier
Venue: Journal of Biological Chemistry
Publisher: Elsevier BV
Published: 2002-10
Volume: 277
Issue: 43
Pages: 41163-41170
ISSN: 0021-9258 (ISSN-L)
DOI: 10.1074/jbc.m202653200
OpenAlex: W2172197126
Cited by: 245
References: 40
Citations by year: 2026: 1 · 2025: 2 · 2024: 3 · 2023: 1 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 6 · 2018: 7 · 2017: 3 · 2016: 6 · 2015: 14 · 2014: 7 · 2013: 21 · 2012: 14
FWCI: 6.60
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by
www.elsevier.com/tdm/userlicense/1.0/ (tdm)
creativecommons.org/licenses/by/4.0/ (vor, 6589 d)
Locations: Journal of Biological Chemistry (publishedVersion, cc-by)
PubMed (publishedVersion)
Funders: Ligue Contre le Cancer
Topics: Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords: hepcidin, C/EBPα, C/EBPβ, HNF4α, iron metabolism, liver development, transcriptional regulation, promoter analysis, iron overload, iron accumulation, hepatocytes, antimicrobial peptides
MeSH terms: Animals, Anti-Bacterial Agents, Base Sequence, DNA, Female, Gene Expression Regulation, Humans, Iron, Liver, Molecular Sequence Data, Promoter Regions, Genetic, RNA, Messenger, Transcription, Genetic, Rats, Sprague-Dawley, CCAAT-Enhancer-Binding Protein-alpha, Antimicrobial Cationic Peptides, Mice, Rats, Hepcidins

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C/EBPα Regulates Hepatic Transcription of Hepcidin, an Antimicrobial Peptide and Regulator of Iron Metabolism

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