Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest
Many environmental and physiological stresses are chronic. Thus, cells are constantly exposed to diverse types of genotoxic insults that challenge genome stability, including those that induce oxidative DNA damage. However, most in vitro studies that model cellular response to oxidative stressors em...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2016
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/27532
- Acceso en línea:
- https://doi.org/10.1016/j.redox.2016.07.004
https://repository.urosario.edu.co/handle/10336/27532
- Palabra clave:
- ROS
Genotoxicity
DNA damage response
Up-regulation of DNA repair genes
G2/M arrest
Adaptation
- Rights
- License
- Abierto (Texto Completo)
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2712031c-3cb5-49bd-86cc-6752396a2b5c-16502a6d7-b93a-4419-8ac6-aca6bd4afee9-110548610-190a136e4-ed1a-43a1-862e-2974cc121428-1897e314b-9b4d-40cf-b3a7-179baaf1b8b3-12020-08-19T14:42:36Z2020-08-19T14:42:36Z2016-10Many environmental and physiological stresses are chronic. Thus, cells are constantly exposed to diverse types of genotoxic insults that challenge genome stability, including those that induce oxidative DNA damage. However, most in vitro studies that model cellular response to oxidative stressors employ short exposures and/or acute stress models. In this study, we tested the hypothesis that chronic and repeated exposure to a micromolar concentration of hydrogen peroxide (H2O2) could activate DNA damage responses, resulting in cellular adaptations. For this purpose, we developed an in vitro model in which we incubated mouse myoblast cells with a steady concentration of ~50 ?M H2O2 for one hour daily for seven days, followed by a final challenge of a 10 or 20X higher dose of H2O2 (0.5 or 1 mM). We report that intermittent long-term exposure to this oxidative stimulus nearly eliminated cell toxicity and significantly decreased genotoxicity (in particular, a >5-fold decreased in double-strand breaks) resulting from subsequent acute exposure to oxidative stress. This protection was associated with cell cycle arrest in G2/M and induction of expression of nine DNA repair genes. Together, this evidence supports an adaptive response to chronic, low-level oxidative stress that results in genomic protection and up-regulated maintenance of cellular homeostasis.application/pdfhttps://doi.org/10.1016/j.redox.2016.07.004ISSN: 2213-2317https://repository.urosario.edu.co/handle/10336/27532engElsevier133124Redox BiologyVol. 9Redox Biology, ISSN: 2213-2317, Vol.9 (2016); pp. 124-133 https://www.sciencedirect.com/science/article/pii/S2213231716300751?via%3DihubAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Redox Biologyinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURROSGenotoxicityDNA damage responseUp-regulation of DNA repair genesG2/M arrestAdaptationDistinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrestRespuesta adaptativa distintiva a la exposición repetida al peróxido de hidrógeno asociada con la regulación positiva de los genes de reparación del ADN y la detención del ciclo celulararticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Santa-Gonzalez, Gloria A.Gomez-Molina, AndreaArcos-Burgos, MauricioMeyer, Joel N.Camargo, MauricioORIGINAL1-s2-0-S2213231716300751-main.pdfapplication/pdf1871232https://repository.urosario.edu.co/bitstreams/8731664d-49df-46e2-aaae-f1e167f173f7/download21f1ed140055ac9e11622ff2e0ef90ffMD51TEXT1-s2-0-S2213231716300751-main.pdf.txt1-s2-0-S2213231716300751-main.pdf.txtExtracted texttext/plain47133https://repository.urosario.edu.co/bitstreams/fd3b5a22-b9e1-45e8-888e-94ea1f65cb0f/downloadb96dde7f7e1849dd29bd213ace63f898MD52THUMBNAIL1-s2-0-S2213231716300751-main.pdf.jpg1-s2-0-S2213231716300751-main.pdf.jpgGenerated Thumbnailimage/jpeg4957https://repository.urosario.edu.co/bitstreams/b0931123-f5ca-41b1-937b-377654430c2b/download14b923e25cdf9bc5ad6d2ccd5428c4d7MD5310336/27532oai:repository.urosario.edu.co:10336/275322021-06-03 00:50:14.553https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest |
dc.title.TranslatedTitle.spa.fl_str_mv |
Respuesta adaptativa distintiva a la exposición repetida al peróxido de hidrógeno asociada con la regulación positiva de los genes de reparación del ADN y la detención del ciclo celular |
title |
Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest |
spellingShingle |
Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest ROS Genotoxicity DNA damage response Up-regulation of DNA repair genes G2/M arrest Adaptation |
title_short |
Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest |
title_full |
Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest |
title_fullStr |
Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest |
title_full_unstemmed |
Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest |
title_sort |
Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest |
dc.subject.keyword.spa.fl_str_mv |
ROS Genotoxicity DNA damage response Up-regulation of DNA repair genes G2/M arrest Adaptation |
topic |
ROS Genotoxicity DNA damage response Up-regulation of DNA repair genes G2/M arrest Adaptation |
description |
Many environmental and physiological stresses are chronic. Thus, cells are constantly exposed to diverse types of genotoxic insults that challenge genome stability, including those that induce oxidative DNA damage. However, most in vitro studies that model cellular response to oxidative stressors employ short exposures and/or acute stress models. In this study, we tested the hypothesis that chronic and repeated exposure to a micromolar concentration of hydrogen peroxide (H2O2) could activate DNA damage responses, resulting in cellular adaptations. For this purpose, we developed an in vitro model in which we incubated mouse myoblast cells with a steady concentration of ~50 ?M H2O2 for one hour daily for seven days, followed by a final challenge of a 10 or 20X higher dose of H2O2 (0.5 or 1 mM). We report that intermittent long-term exposure to this oxidative stimulus nearly eliminated cell toxicity and significantly decreased genotoxicity (in particular, a >5-fold decreased in double-strand breaks) resulting from subsequent acute exposure to oxidative stress. This protection was associated with cell cycle arrest in G2/M and induction of expression of nine DNA repair genes. Together, this evidence supports an adaptive response to chronic, low-level oxidative stress that results in genomic protection and up-regulated maintenance of cellular homeostasis. |
publishDate |
2016 |
dc.date.created.spa.fl_str_mv |
2016-10 |
dc.date.accessioned.none.fl_str_mv |
2020-08-19T14:42:36Z |
dc.date.available.none.fl_str_mv |
2020-08-19T14:42:36Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1016/j.redox.2016.07.004 |
dc.identifier.issn.none.fl_str_mv |
ISSN: 2213-2317 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/27532 |
url |
https://doi.org/10.1016/j.redox.2016.07.004 https://repository.urosario.edu.co/handle/10336/27532 |
identifier_str_mv |
ISSN: 2213-2317 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
133 |
dc.relation.citationStartPage.none.fl_str_mv |
124 |
dc.relation.citationTitle.none.fl_str_mv |
Redox Biology |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 9 |
dc.relation.ispartof.spa.fl_str_mv |
Redox Biology, ISSN: 2213-2317, Vol.9 (2016); pp. 124-133 |
dc.relation.uri.spa.fl_str_mv |
https://www.sciencedirect.com/science/article/pii/S2213231716300751?via%3Dihub |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
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application/pdf |
dc.publisher.spa.fl_str_mv |
Elsevier |
dc.source.spa.fl_str_mv |
Redox Biology |
institution |
Universidad del Rosario |
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instname:Universidad del Rosario |
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reponame:Repositorio Institucional EdocUR |
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