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On Iron Metabolism and Its Regulation

Iron is a critical metal for several vital biological processes. Most of the body’s iron is bound to hemoglobin in erythrocytes. Iron from senescent red blood cells is recycled by macrophages in the spleen, liver and bone marrow. Dietary iron is taken up by the divalent metal transporter 1 (DMT1) in...

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Autores principales: Vogt, Anne-Cathrine S., Arsiwala, Tasneem, Mohsen, Mona, Vogel, Monique, Manolova, Vania, Bachmann, Martin F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123811/
https://www.ncbi.nlm.nih.gov/pubmed/33925597
http://dx.doi.org/10.3390/ijms22094591
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author Vogt, Anne-Cathrine S.
Arsiwala, Tasneem
Mohsen, Mona
Vogel, Monique
Manolova, Vania
Bachmann, Martin F.
author_facet Vogt, Anne-Cathrine S.
Arsiwala, Tasneem
Mohsen, Mona
Vogel, Monique
Manolova, Vania
Bachmann, Martin F.
author_sort Vogt, Anne-Cathrine S.
collection PubMed
description Iron is a critical metal for several vital biological processes. Most of the body’s iron is bound to hemoglobin in erythrocytes. Iron from senescent red blood cells is recycled by macrophages in the spleen, liver and bone marrow. Dietary iron is taken up by the divalent metal transporter 1 (DMT1) in enterocytes and transported to portal blood via ferroportin (FPN), where it is bound to transferrin and taken up by hepatocytes, macrophages and bone marrow cells via transferrin receptor 1 (TfR1). While most of the physiologically active iron is bound hemoglobin, the major storage of most iron occurs in the liver in a ferritin-bound fashion. In response to an increased iron load, hepatocytes secrete the peptide hormone hepcidin, which binds to and induces internalization and degradation of the iron transporter FPN, thus controlling the amount of iron released from the cells into the blood. This review summarizes the key mechanisms and players involved in cellular and systemic iron regulation.
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spelling pubmed-81238112021-05-16 On Iron Metabolism and Its Regulation Vogt, Anne-Cathrine S. Arsiwala, Tasneem Mohsen, Mona Vogel, Monique Manolova, Vania Bachmann, Martin F. Int J Mol Sci Review Iron is a critical metal for several vital biological processes. Most of the body’s iron is bound to hemoglobin in erythrocytes. Iron from senescent red blood cells is recycled by macrophages in the spleen, liver and bone marrow. Dietary iron is taken up by the divalent metal transporter 1 (DMT1) in enterocytes and transported to portal blood via ferroportin (FPN), where it is bound to transferrin and taken up by hepatocytes, macrophages and bone marrow cells via transferrin receptor 1 (TfR1). While most of the physiologically active iron is bound hemoglobin, the major storage of most iron occurs in the liver in a ferritin-bound fashion. In response to an increased iron load, hepatocytes secrete the peptide hormone hepcidin, which binds to and induces internalization and degradation of the iron transporter FPN, thus controlling the amount of iron released from the cells into the blood. This review summarizes the key mechanisms and players involved in cellular and systemic iron regulation. MDPI 2021-04-27 /pmc/articles/PMC8123811/ /pubmed/33925597 http://dx.doi.org/10.3390/ijms22094591 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Vogt, Anne-Cathrine S.
Arsiwala, Tasneem
Mohsen, Mona
Vogel, Monique
Manolova, Vania
Bachmann, Martin F.
On Iron Metabolism and Its Regulation
title On Iron Metabolism and Its Regulation
title_full On Iron Metabolism and Its Regulation
title_fullStr On Iron Metabolism and Its Regulation
title_full_unstemmed On Iron Metabolism and Its Regulation
title_short On Iron Metabolism and Its Regulation
title_sort on iron metabolism and its regulation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123811/
https://www.ncbi.nlm.nih.gov/pubmed/33925597
http://dx.doi.org/10.3390/ijms22094591
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