Cell to Cell Variability of Radiation-Induced Foci

Most studies that aim to understand the interactions between different types of photon radiation and cellular DNA assume homogeneous cell irradiation, with all cells receiving the same amount of energy. The level of DNA damage is therefore generally determined by averaging it over the entire populat...

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Autores: Gruel, Gaëtan, Villagrasa, Carmen, Voisin, Pascale, Clairand, Isabelle, Benderitter, Marc, Bottollier-Depois, Jean-François, Barquinero, Joan Francesc|||0000-0003-0084-5268
Formato: artículo
Fecha de publicación:2016
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:170613
Acesso em linha:https://ddd.uab.cat/record/170613
https://dx.doi.org/urn:doi:10.1371/journal.pone.0145786
Access Level:acceso abierto
Palavra-chave:Confocal microscopy
DNA damage
Ionizing radiation
Cell cycle and cell division
Photons
Focal planes
Endothelial cells
Flow cytometry
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spelling Cell to Cell Variability of Radiation-Induced Focirelation between Observed Damage and Energy DepositionGruel, GaëtanVillagrasa, CarmenVoisin, PascaleClairand, IsabelleBenderitter, MarcBottollier-Depois, Jean-FrançoisBarquinero, Joan Francesc|||0000-0003-0084-5268Confocal microscopyDNA damageIonizing radiationCell cycle and cell divisionPhotonsFocal planesEndothelial cellsFlow cytometryMost studies that aim to understand the interactions between different types of photon radiation and cellular DNA assume homogeneous cell irradiation, with all cells receiving the same amount of energy. The level of DNA damage is therefore generally determined by averaging it over the entire population of exposed cells. However, evaluating the molecular consequences of a stochastic phenomenon such as energy deposition of ionizing radiation by measuring only an average effect may not be sufficient for understanding some aspects of the cellular response to this radiation. The variance among the cells associated with this average effect may also be important for the behaviour of irradiated tissue. In this study, we accurately estimated the distribution of the number of radiation-induced γH2AX foci (RIF) per cell nucleus in a large population of endothelial cells exposed to 3 macroscopic doses of gamma rays from 60Co. The number of RIF varied significantly and reproducibly from cell to cell, with its relative standard deviation ranging from 36% to 18% depending on the macroscopic dose delivered. Interestingly, this relative cell-to-cell variability increased as the dose decreased, contrary to the mean RIF count per cell. This result shows that the dose effect, in terms of the number of DNA lesions indicated by RIF is not as simple as a purely proportional relation in which relative SD is constant with dose. To analyse the origins of this observed variability, we calculated the spread of the specific energy distribution for the different target volumes and subvolumes in which RIF can be generated. Variances, standard deviations and relative standard deviations all changed similarly from dose to dose for biological and calculated microdosimetric values. This similarity is an important argument that supports the hypothesis of the conservation of the association between the number of RIF per nucleus and the specific energy per DNA molecule. This comparison allowed us to calculate a volume of 1.6 μm3 for which the spread of the specific energy distribution could explain the entire variability of RIF counts per cell in an exposed cell population. The definition of this volume may allow to use a microdosimetric quantity to predict heterogeneity in DNA damage. Moreover, this value is consistent with the order of magnitude of the volume occupied by the hydrated sugar-phosphate backbone of the DNA molecule, which is the part of the DNA molecule responsible for strand breaks. 22016-01-0120162016-01-01Articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/170613https://dx.doi.org/urn:doi:10.1371/journal.pone.0145786reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengopen accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:1706132026-06-06T12:50:31Z
dc.title.none.fl_str_mv Cell to Cell Variability of Radiation-Induced Foci
relation between Observed Damage and Energy Deposition
title Cell to Cell Variability of Radiation-Induced Foci
spellingShingle Cell to Cell Variability of Radiation-Induced Foci
Gruel, Gaëtan
Confocal microscopy
DNA damage
Ionizing radiation
Cell cycle and cell division
Photons
Focal planes
Endothelial cells
Flow cytometry
title_short Cell to Cell Variability of Radiation-Induced Foci
title_full Cell to Cell Variability of Radiation-Induced Foci
title_fullStr Cell to Cell Variability of Radiation-Induced Foci
title_full_unstemmed Cell to Cell Variability of Radiation-Induced Foci
title_sort Cell to Cell Variability of Radiation-Induced Foci
dc.creator.none.fl_str_mv Gruel, Gaëtan
Villagrasa, Carmen
Voisin, Pascale
Clairand, Isabelle
Benderitter, Marc
Bottollier-Depois, Jean-François
Barquinero, Joan Francesc|||0000-0003-0084-5268
author Gruel, Gaëtan
author_facet Gruel, Gaëtan
Villagrasa, Carmen
Voisin, Pascale
Clairand, Isabelle
Benderitter, Marc
Bottollier-Depois, Jean-François
Barquinero, Joan Francesc|||0000-0003-0084-5268
author_role author
author2 Villagrasa, Carmen
Voisin, Pascale
Clairand, Isabelle
Benderitter, Marc
Bottollier-Depois, Jean-François
Barquinero, Joan Francesc|||0000-0003-0084-5268
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv Confocal microscopy
DNA damage
Ionizing radiation
Cell cycle and cell division
Photons
Focal planes
Endothelial cells
Flow cytometry
topic Confocal microscopy
DNA damage
Ionizing radiation
Cell cycle and cell division
Photons
Focal planes
Endothelial cells
Flow cytometry
description Most studies that aim to understand the interactions between different types of photon radiation and cellular DNA assume homogeneous cell irradiation, with all cells receiving the same amount of energy. The level of DNA damage is therefore generally determined by averaging it over the entire population of exposed cells. However, evaluating the molecular consequences of a stochastic phenomenon such as energy deposition of ionizing radiation by measuring only an average effect may not be sufficient for understanding some aspects of the cellular response to this radiation. The variance among the cells associated with this average effect may also be important for the behaviour of irradiated tissue. In this study, we accurately estimated the distribution of the number of radiation-induced γH2AX foci (RIF) per cell nucleus in a large population of endothelial cells exposed to 3 macroscopic doses of gamma rays from 60Co. The number of RIF varied significantly and reproducibly from cell to cell, with its relative standard deviation ranging from 36% to 18% depending on the macroscopic dose delivered. Interestingly, this relative cell-to-cell variability increased as the dose decreased, contrary to the mean RIF count per cell. This result shows that the dose effect, in terms of the number of DNA lesions indicated by RIF is not as simple as a purely proportional relation in which relative SD is constant with dose. To analyse the origins of this observed variability, we calculated the spread of the specific energy distribution for the different target volumes and subvolumes in which RIF can be generated. Variances, standard deviations and relative standard deviations all changed similarly from dose to dose for biological and calculated microdosimetric values. This similarity is an important argument that supports the hypothesis of the conservation of the association between the number of RIF per nucleus and the specific energy per DNA molecule. This comparison allowed us to calculate a volume of 1.6 μm3 for which the spread of the specific energy distribution could explain the entire variability of RIF counts per cell in an exposed cell population. The definition of this volume may allow to use a microdosimetric quantity to predict heterogeneity in DNA damage. Moreover, this value is consistent with the order of magnitude of the volume occupied by the hydrated sugar-phosphate backbone of the DNA molecule, which is the part of the DNA molecule responsible for strand breaks.
publishDate 2016
dc.date.none.fl_str_mv 2
2016-01-01
2016
2016-01-01
dc.type.none.fl_str_mv Article
http://purl.org/coar/resource_type/c_6501
VoR
http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://ddd.uab.cat/record/170613
https://dx.doi.org/urn:doi:10.1371/journal.pone.0145786
url https://ddd.uab.cat/record/170613
https://dx.doi.org/urn:doi:10.1371/journal.pone.0145786
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by/4.0/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Dipòsit Digital de Documents de la UAB
instname:Universitat Autònoma de Barcelona
instname_str Universitat Autònoma de Barcelona
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collection Dipòsit Digital de Documents de la UAB
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