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Dual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic Effects

Iron is essential for life, while also being potentially harmful. Therefore, its level is strictly monitored and complex pathways have evolved to keep iron safely bound to transport or storage proteins, thereby maintaining homeostasis at the cellular and systemic levels. These sequestration mechanis...

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Detalles Bibliográficos
Autores principales: Gammella, Elena, Recalcati, Stefania, Cairo, Gaetano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783558/
https://www.ncbi.nlm.nih.gov/pubmed/27006749
http://dx.doi.org/10.1155/2016/8629024
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author Gammella, Elena
Recalcati, Stefania
Cairo, Gaetano
author_facet Gammella, Elena
Recalcati, Stefania
Cairo, Gaetano
author_sort Gammella, Elena
collection PubMed
description Iron is essential for life, while also being potentially harmful. Therefore, its level is strictly monitored and complex pathways have evolved to keep iron safely bound to transport or storage proteins, thereby maintaining homeostasis at the cellular and systemic levels. These sequestration mechanisms ensure that mildly reactive oxygen species like anion superoxide and hydrogen peroxide, which are continuously generated in cells living under aerobic conditions, keep their physiologic role in cell signaling while escaping iron-catalyzed transformation in the highly toxic hydroxyl radical. In this review, we describe the multifaceted systems regulating cellular and body iron homeostasis and discuss how altered iron balance may lead to oxidative damage in some pathophysiological settings.
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spelling pubmed-47835582016-03-22 Dual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic Effects Gammella, Elena Recalcati, Stefania Cairo, Gaetano Oxid Med Cell Longev Review Article Iron is essential for life, while also being potentially harmful. Therefore, its level is strictly monitored and complex pathways have evolved to keep iron safely bound to transport or storage proteins, thereby maintaining homeostasis at the cellular and systemic levels. These sequestration mechanisms ensure that mildly reactive oxygen species like anion superoxide and hydrogen peroxide, which are continuously generated in cells living under aerobic conditions, keep their physiologic role in cell signaling while escaping iron-catalyzed transformation in the highly toxic hydroxyl radical. In this review, we describe the multifaceted systems regulating cellular and body iron homeostasis and discuss how altered iron balance may lead to oxidative damage in some pathophysiological settings. Hindawi Publishing Corporation 2016 2016-02-24 /pmc/articles/PMC4783558/ /pubmed/27006749 http://dx.doi.org/10.1155/2016/8629024 Text en Copyright © 2016 Elena Gammella et al. https://creativecommons.org/licenses/by/4.0/ 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
Gammella, Elena
Recalcati, Stefania
Cairo, Gaetano
Dual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic Effects
title Dual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic Effects
title_full Dual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic Effects
title_fullStr Dual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic Effects
title_full_unstemmed Dual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic Effects
title_short Dual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic Effects
title_sort dual role of ros as signal and stress agents: iron tips the balance in favor of toxic effects
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783558/
https://www.ncbi.nlm.nih.gov/pubmed/27006749
http://dx.doi.org/10.1155/2016/8629024
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