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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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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. |
format | Online Article Text |
id | pubmed-3226344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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