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Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development

The first mature cells to arise in the developing mammalian embryo belong to the erythroid lineage. This highlights the immediacy of the need for red blood cells during embryogenesis and for survival. Linked with this pressure is the necessity of the embryo to obtain and transport iron, synthesize h...

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Detalles Bibliográficos
Autores principales: Fraser, Stuart T., Midwinter, Robyn G., Berger, Birgit S., Stocker, Roland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226344/
https://www.ncbi.nlm.nih.gov/pubmed/22162689
http://dx.doi.org/10.1155/2011/473709
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author Fraser, Stuart T.
Midwinter, Robyn G.
Berger, Birgit S.
Stocker, Roland
author_facet Fraser, Stuart T.
Midwinter, Robyn G.
Berger, Birgit S.
Stocker, Roland
author_sort Fraser, Stuart T.
collection PubMed
description The first mature cells to arise in the developing mammalian embryo belong to the erythroid lineage. This highlights the immediacy of the need for red blood cells during embryogenesis and for survival. Linked with this pressure is the necessity of the embryo to obtain and transport iron, synthesize hemoglobin, and then dispose of the potentially toxic heme via the stress-induced protein heme oxygenase-1 (HO-1, encoded by Hmox1 in the mouse). Null mutation of Hmox1 results in significant embryonic mortality as well as anemia and defective iron recycling. Here, we discuss the interrelated nature of this critical enzyme with iron trafficking, erythroid cell function, and embryonic survival.
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spelling pubmed-32263442011-12-08 Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development Fraser, Stuart T. Midwinter, Robyn G. Berger, Birgit S. Stocker, Roland Adv Hematol Review Article The first mature cells to arise in the developing mammalian embryo belong to the erythroid lineage. This highlights the immediacy of the need for red blood cells during embryogenesis and for survival. Linked with this pressure is the necessity of the embryo to obtain and transport iron, synthesize hemoglobin, and then dispose of the potentially toxic heme via the stress-induced protein heme oxygenase-1 (HO-1, encoded by Hmox1 in the mouse). Null mutation of Hmox1 results in significant embryonic mortality as well as anemia and defective iron recycling. Here, we discuss the interrelated nature of this critical enzyme with iron trafficking, erythroid cell function, and embryonic survival. Hindawi Publishing Corporation 2011 2011-11-20 /pmc/articles/PMC3226344/ /pubmed/22162689 http://dx.doi.org/10.1155/2011/473709 Text en Copyright © 2011 Stuart T. Fraser et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Fraser, Stuart T.
Midwinter, Robyn G.
Berger, Birgit S.
Stocker, Roland
Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development
title Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development
title_full Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development
title_fullStr Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development
title_full_unstemmed Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development
title_short Heme Oxygenase-1: A Critical Link between Iron Metabolism, Erythropoiesis, and Development
title_sort heme oxygenase-1: a critical link between iron metabolism, erythropoiesis, and development
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226344/
https://www.ncbi.nlm.nih.gov/pubmed/22162689
http://dx.doi.org/10.1155/2011/473709
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