Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025:1480:89-102.
doi: 10.1007/978-3-031-92033-2_7.

Hepcidin and Tissue-Specific Iron Regulatory Networks

Affiliations
Review

Hepcidin and Tissue-Specific Iron Regulatory Networks

Samira Lakhal-Littleton et al. Adv Exp Med Biol. 2025.

Abstract

Hepcidin is primarily secreted by the liver and functions as an endocrine hormone. However, a growing number of studies show that hepcidin can also be produced locally by other cells and organs, where it acts in an autocrine/paracrine manner to mediate important iron-dependent pathways. These pathways can operate under normal homeostatic conditions or become relevant in pathophysiological conditions (inflammation, infection, cancer, liver disease, myocardial infarction, etc.). This chapter will delve into the local roles of hepcidin, highlighting its unconventional functions in barrier maintenance, host defense, growth, tissue housekeeping, and injury repair.

Keywords: Barrier functions; Cell division; Endocrine control; Hepcidin; Host defense; Local iron regulation; Repair; Tissue housekeeping.

PubMed Disclaimer

References

    1. Abboud E, Chrayteh D, Boussetta N et al (2024) Skin hepcidin initiates psoriasiform skin inflammation via Fe-driven hyperproliferation and neutrophil recruitment. Nat Commun 15:6718. https://doi.org/10.1038/s41467-024-50993-8 - DOI - PubMed - PMC
    1. Armitage AE, Eddowes LA, Gileadi U, Cole S, Spottiswoode N, Selvakumar TA, Ho LP, Townsend AR, Drakesmith H (2011) Hepcidin regulation by innate immune and infectious stimuli. Blood 118(15):4129–4139. https://doi.org/10.1182/blood-2011-04-351957
    1. Banerjee S, Datta R (2020) Leishmania infection triggers hepcidin-mediated proteasomal degradation of Nramp1 to increase phagolysosomal iron availability. Cell Microbiol 22:e13253. https://doi.org/10.1111/cmi.13253 - DOI - PubMed
    1. Bart NK, Curtis MK, Cheng HY et al (2016) Elevation of iron storage in humans attenuates the pulmonary vascular response to hypoxia. J Appl Physiol 121(2):537–544. https://doi.org/10.1152/japplphysiol.00032.2016 - DOI - PubMed - PMC
    1. Bek SG, Üstüner B, Eren N, Sentürk Z, Gönüllü BK (1992) The effect of hepcidin on components of metabolic syndrome in chronic kidney disease: a cross-sectional study. Rev Assoc Med Bras 66(8):1100–1107. https://doi.org/10.1590/1806-9282.66.8.1100 - DOI

LinkOut - more resources