Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem Cells

Human adipose-derived mesenchymal stem cells (hADMSCs) are recognized as a potential tool in cell tissue therapy because of their capacity to proliferate and differentiate in vitro. Several studies have addressed their use in regenerative medicine; however, little is known regarding their response t...

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Main Authors: Mahara Valverde, Jonathan Lozano-Salgado, Paola Fortini, Maria Alexandra Rodriguez-Sastre, Emilio Rojas, Eugenia Dogliotti
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2018/1615497
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spelling doaj-ace8d3fd15574cf5a084b96ec7be22632020-11-25T02:52:08ZengHindawi LimitedStem Cells International1687-966X1687-96782018-01-01201810.1155/2018/16154971615497Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem CellsMahara Valverde0Jonathan Lozano-Salgado1Paola Fortini2Maria Alexandra Rodriguez-Sastre3Emilio Rojas4Eugenia Dogliotti5Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, C.U. 04510, MexicoInstituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, C.U. 04510, MexicoDepartment of Environment and Health, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Roma, ItalyInstituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, C.U. 04510, MexicoInstituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, C.U. 04510, MexicoDepartment of Environment and Health, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Roma, ItalyHuman adipose-derived mesenchymal stem cells (hADMSCs) are recognized as a potential tool in cell tissue therapy because of their capacity to proliferate and differentiate in vitro. Several studies have addressed their use in regenerative medicine; however, little is known regarding their response to DNA damage and in particular to the reactive oxygen species (ROS) that are present in the microenvironment of implantation. In this study, we used the ROS-inducing agent hydrogen peroxide to explore the responses of (1) hADMSCs and (2) derived terminally differentiated adipocytes to oxidatively generated DNA damage. Using single cell gel electrophoresis, a dose-related increase was found for both DNA breaks and oxidative lesions (formamidopyrimidine DNA glycosylase-sensitive sites) upon exposure of hADMSCs to hydrogen peroxide. DNA repair capacity of hADMSCs was affected in cells exposed to 150 and 200 μM of hydrogen peroxide. An increase in the basal levels of DNA breaks and oxidative DNA lesions was observed through adipocyte differentiation. In addition, hydrogen peroxide-induced DNA damage increased through adipocyte differentiation; DNA repair capacity also decreased. This study is the first follow-up report on DNA repair capacity during adipogenic differentiation. Remarkably, in terminally differentiated adipocytes, DNA breakage repair is abolished while the repair of DNA oxidative lesions remains efficient.http://dx.doi.org/10.1155/2018/1615497
collection DOAJ
language English
format Article
sources DOAJ
author Mahara Valverde
Jonathan Lozano-Salgado
Paola Fortini
Maria Alexandra Rodriguez-Sastre
Emilio Rojas
Eugenia Dogliotti
spellingShingle Mahara Valverde
Jonathan Lozano-Salgado
Paola Fortini
Maria Alexandra Rodriguez-Sastre
Emilio Rojas
Eugenia Dogliotti
Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem Cells
Stem Cells International
author_facet Mahara Valverde
Jonathan Lozano-Salgado
Paola Fortini
Maria Alexandra Rodriguez-Sastre
Emilio Rojas
Eugenia Dogliotti
author_sort Mahara Valverde
title Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem Cells
title_short Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem Cells
title_full Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem Cells
title_fullStr Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem Cells
title_full_unstemmed Hydrogen Peroxide-Induced DNA Damage and Repair through the Differentiation of Human Adipose-Derived Mesenchymal Stem Cells
title_sort hydrogen peroxide-induced dna damage and repair through the differentiation of human adipose-derived mesenchymal stem cells
publisher Hindawi Limited
series Stem Cells International
issn 1687-966X
1687-9678
publishDate 2018-01-01
description Human adipose-derived mesenchymal stem cells (hADMSCs) are recognized as a potential tool in cell tissue therapy because of their capacity to proliferate and differentiate in vitro. Several studies have addressed their use in regenerative medicine; however, little is known regarding their response to DNA damage and in particular to the reactive oxygen species (ROS) that are present in the microenvironment of implantation. In this study, we used the ROS-inducing agent hydrogen peroxide to explore the responses of (1) hADMSCs and (2) derived terminally differentiated adipocytes to oxidatively generated DNA damage. Using single cell gel electrophoresis, a dose-related increase was found for both DNA breaks and oxidative lesions (formamidopyrimidine DNA glycosylase-sensitive sites) upon exposure of hADMSCs to hydrogen peroxide. DNA repair capacity of hADMSCs was affected in cells exposed to 150 and 200 μM of hydrogen peroxide. An increase in the basal levels of DNA breaks and oxidative DNA lesions was observed through adipocyte differentiation. In addition, hydrogen peroxide-induced DNA damage increased through adipocyte differentiation; DNA repair capacity also decreased. This study is the first follow-up report on DNA repair capacity during adipogenic differentiation. Remarkably, in terminally differentiated adipocytes, DNA breakage repair is abolished while the repair of DNA oxidative lesions remains efficient.
url http://dx.doi.org/10.1155/2018/1615497
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