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Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis

Liver cells communicate with the extracellular environment to take up nutrients via endocytosis. Iron uptake is essential for metabolic activities and cell homeostasis. Here, we investigated the role of the endocytic system for maintaining iron homeostasis. We specifically depleted the small GTPase...

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Autores principales: Metzendorf, Christoph, Zeigerer, Anja, Seifert, Sarah, Sparla, Richard, Najafi, Bahar, Canonne-Hergaux, François, Zerial, Marino, Muckenthaler, Martina U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481338/
https://www.ncbi.nlm.nih.gov/pubmed/28642463
http://dx.doi.org/10.1038/s41598-017-02898-4
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author Metzendorf, Christoph
Zeigerer, Anja
Seifert, Sarah
Sparla, Richard
Najafi, Bahar
Canonne-Hergaux, François
Zerial, Marino
Muckenthaler, Martina U.
author_facet Metzendorf, Christoph
Zeigerer, Anja
Seifert, Sarah
Sparla, Richard
Najafi, Bahar
Canonne-Hergaux, François
Zerial, Marino
Muckenthaler, Martina U.
author_sort Metzendorf, Christoph
collection PubMed
description Liver cells communicate with the extracellular environment to take up nutrients via endocytosis. Iron uptake is essential for metabolic activities and cell homeostasis. Here, we investigated the role of the endocytic system for maintaining iron homeostasis. We specifically depleted the small GTPase Rab5 in the mouse liver, causing a transient loss of the entire endo-lysosomal system. Strikingly, endosome depletion led to a fast reduction of hepatic iron levels, which was preceded by an increased abundance of the iron exporter ferroportin. Compensatory changes in livers of Rab5-depleted mice include increased expression of transferrin receptor 1 as well as reduced expression of the iron-regulatory hormone hepcidin. Serum iron indices (serum iron, free iron binding capacity and total iron binding capacity) in Rab5-KD mice were increased, consistent with an elevated splenic and hepatic iron export. Our data emphasize the critical importance of the endosomal compartments in hepatocytes to maintain hepatic and systemic iron homeostasis in vivo. The short time period (between day four and five) upon which these changes occur underscore the fast dynamics of the liver iron pool.
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spelling pubmed-54813382017-06-26 Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis Metzendorf, Christoph Zeigerer, Anja Seifert, Sarah Sparla, Richard Najafi, Bahar Canonne-Hergaux, François Zerial, Marino Muckenthaler, Martina U. Sci Rep Article Liver cells communicate with the extracellular environment to take up nutrients via endocytosis. Iron uptake is essential for metabolic activities and cell homeostasis. Here, we investigated the role of the endocytic system for maintaining iron homeostasis. We specifically depleted the small GTPase Rab5 in the mouse liver, causing a transient loss of the entire endo-lysosomal system. Strikingly, endosome depletion led to a fast reduction of hepatic iron levels, which was preceded by an increased abundance of the iron exporter ferroportin. Compensatory changes in livers of Rab5-depleted mice include increased expression of transferrin receptor 1 as well as reduced expression of the iron-regulatory hormone hepcidin. Serum iron indices (serum iron, free iron binding capacity and total iron binding capacity) in Rab5-KD mice were increased, consistent with an elevated splenic and hepatic iron export. Our data emphasize the critical importance of the endosomal compartments in hepatocytes to maintain hepatic and systemic iron homeostasis in vivo. The short time period (between day four and five) upon which these changes occur underscore the fast dynamics of the liver iron pool. Nature Publishing Group UK 2017-06-22 /pmc/articles/PMC5481338/ /pubmed/28642463 http://dx.doi.org/10.1038/s41598-017-02898-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Metzendorf, Christoph
Zeigerer, Anja
Seifert, Sarah
Sparla, Richard
Najafi, Bahar
Canonne-Hergaux, François
Zerial, Marino
Muckenthaler, Martina U.
Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis
title Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis
title_full Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis
title_fullStr Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis
title_full_unstemmed Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis
title_short Acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis
title_sort acute loss of the hepatic endo-lysosomal system in vivo causes compensatory changes in iron homeostasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481338/
https://www.ncbi.nlm.nih.gov/pubmed/28642463
http://dx.doi.org/10.1038/s41598-017-02898-4
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