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Modulation of Oxidative Status by Normoxia and Hypoxia on Cultures of Human Dermal Fibroblasts: How Does It Affect Cell Aging?

Reactive oxygen species (ROS) production in the skin is among the highest compared to other organs, and a clear correlation exists between ROS production and skin aging. Many attempts are underway to reduce oxidative stress in the skin by topical treatment or supplementation with antioxidants/cosmec...

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Autores principales: Damiani, Elisabetta, Brugè, Francesca, Cirilli, Ilenia, Marcheggiani, Fabio, Olivieri, Fabiola, Armeni, Tatiana, Cianfruglia, Laura, Giuliani, Angelica, Orlando, Patrick, Tiano, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199889/
https://www.ncbi.nlm.nih.gov/pubmed/30405877
http://dx.doi.org/10.1155/2018/5469159
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author Damiani, Elisabetta
Brugè, Francesca
Cirilli, Ilenia
Marcheggiani, Fabio
Olivieri, Fabiola
Armeni, Tatiana
Cianfruglia, Laura
Giuliani, Angelica
Orlando, Patrick
Tiano, Luca
author_facet Damiani, Elisabetta
Brugè, Francesca
Cirilli, Ilenia
Marcheggiani, Fabio
Olivieri, Fabiola
Armeni, Tatiana
Cianfruglia, Laura
Giuliani, Angelica
Orlando, Patrick
Tiano, Luca
author_sort Damiani, Elisabetta
collection PubMed
description Reactive oxygen species (ROS) production in the skin is among the highest compared to other organs, and a clear correlation exists between ROS production and skin aging. Many attempts are underway to reduce oxidative stress in the skin by topical treatment or supplementation with antioxidants/cosmeceuticals, and cultures of human dermal fibroblasts (HDF) are widely used for these studies. Here, we examined the influence of oxygen tension on cell aging in HDF and how this impacted ROS production, the enzymatic and nonenzymatic antioxidant response system, and the efficacy of this defense system in limiting DNA damage and in modulating gene expression of proteins involved in the extracellular matrix, linked to skin aging. We investigated a selection of parameters that represent and reflect the behavior of cellular responses to aging and oxygen tension. Serial passaging of HDF under normoxia (21%) and hypoxia (5%) leads to cell aging as confirmed by β-galactosidase activity, p16 expression, and proliferation rate. However, in HDF under 21% O(2), markers of aging were significantly increased compared to those under 5% O(2) at matched cell passages despite having lower levels of intracellular ROS and higher levels of CoQ(10), total GSH, SOD1, SOD3, and mitochondrial superoxide anion. miRNA-181a, which is known to be upregulated in HDF senescence, was also analyzed, and indeed, its expression was significantly increased in old cells at 21% O(2) compared to those at 5% O(2). Upregulation of MMP1 and downregulation of COL1A1 along with increased DNA damage were also observed under 21% O(2) vs 5% O(2). The data highlight that chronic exposure to atmospheric 21% O(2) is able to trigger hormetic adaptive responses in HDF that however fail, in the long term, to prevent cellular aging. This information could be useful in further investigating molecular mechanisms involved in adaptation of skin fibroblasts to oxidative stress and may provide useful hints in addressing antiaging strategies.
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spelling pubmed-61998892018-11-07 Modulation of Oxidative Status by Normoxia and Hypoxia on Cultures of Human Dermal Fibroblasts: How Does It Affect Cell Aging? Damiani, Elisabetta Brugè, Francesca Cirilli, Ilenia Marcheggiani, Fabio Olivieri, Fabiola Armeni, Tatiana Cianfruglia, Laura Giuliani, Angelica Orlando, Patrick Tiano, Luca Oxid Med Cell Longev Research Article Reactive oxygen species (ROS) production in the skin is among the highest compared to other organs, and a clear correlation exists between ROS production and skin aging. Many attempts are underway to reduce oxidative stress in the skin by topical treatment or supplementation with antioxidants/cosmeceuticals, and cultures of human dermal fibroblasts (HDF) are widely used for these studies. Here, we examined the influence of oxygen tension on cell aging in HDF and how this impacted ROS production, the enzymatic and nonenzymatic antioxidant response system, and the efficacy of this defense system in limiting DNA damage and in modulating gene expression of proteins involved in the extracellular matrix, linked to skin aging. We investigated a selection of parameters that represent and reflect the behavior of cellular responses to aging and oxygen tension. Serial passaging of HDF under normoxia (21%) and hypoxia (5%) leads to cell aging as confirmed by β-galactosidase activity, p16 expression, and proliferation rate. However, in HDF under 21% O(2), markers of aging were significantly increased compared to those under 5% O(2) at matched cell passages despite having lower levels of intracellular ROS and higher levels of CoQ(10), total GSH, SOD1, SOD3, and mitochondrial superoxide anion. miRNA-181a, which is known to be upregulated in HDF senescence, was also analyzed, and indeed, its expression was significantly increased in old cells at 21% O(2) compared to those at 5% O(2). Upregulation of MMP1 and downregulation of COL1A1 along with increased DNA damage were also observed under 21% O(2) vs 5% O(2). The data highlight that chronic exposure to atmospheric 21% O(2) is able to trigger hormetic adaptive responses in HDF that however fail, in the long term, to prevent cellular aging. This information could be useful in further investigating molecular mechanisms involved in adaptation of skin fibroblasts to oxidative stress and may provide useful hints in addressing antiaging strategies. Hindawi 2018-09-23 /pmc/articles/PMC6199889/ /pubmed/30405877 http://dx.doi.org/10.1155/2018/5469159 Text en Copyright © 2018 Elisabetta Damiani et al. http://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 Research Article
Damiani, Elisabetta
Brugè, Francesca
Cirilli, Ilenia
Marcheggiani, Fabio
Olivieri, Fabiola
Armeni, Tatiana
Cianfruglia, Laura
Giuliani, Angelica
Orlando, Patrick
Tiano, Luca
Modulation of Oxidative Status by Normoxia and Hypoxia on Cultures of Human Dermal Fibroblasts: How Does It Affect Cell Aging?
title Modulation of Oxidative Status by Normoxia and Hypoxia on Cultures of Human Dermal Fibroblasts: How Does It Affect Cell Aging?
title_full Modulation of Oxidative Status by Normoxia and Hypoxia on Cultures of Human Dermal Fibroblasts: How Does It Affect Cell Aging?
title_fullStr Modulation of Oxidative Status by Normoxia and Hypoxia on Cultures of Human Dermal Fibroblasts: How Does It Affect Cell Aging?
title_full_unstemmed Modulation of Oxidative Status by Normoxia and Hypoxia on Cultures of Human Dermal Fibroblasts: How Does It Affect Cell Aging?
title_short Modulation of Oxidative Status by Normoxia and Hypoxia on Cultures of Human Dermal Fibroblasts: How Does It Affect Cell Aging?
title_sort modulation of oxidative status by normoxia and hypoxia on cultures of human dermal fibroblasts: how does it affect cell aging?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199889/
https://www.ncbi.nlm.nih.gov/pubmed/30405877
http://dx.doi.org/10.1155/2018/5469159
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