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Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials

Human dental pulp stem cells (HDPSCs) are of special relevance in future regenerative dental therapies. Characterizing cytotoxicity and genotoxicity produced by endodontic materials is required to evaluate the potential for regeneration of injured tissues in future strategies combining regenerative...

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Autores principales: Victoria-Escandell, Alejandro, Ibañez-Cabellos, José Santiago, de Cutanda, Sergio Bañuls-Sánchez, Berenguer-Pascual, Ester, Beltrán-García, Jesús, García-López, Eva, Pallardó, Federico V., García-Giménez, José Luis, Pallarés-Sabater, Antonio, Zarzosa-López, Ignacio, Monterde, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511667/
https://www.ncbi.nlm.nih.gov/pubmed/28751918
http://dx.doi.org/10.1155/2017/8920356
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author Victoria-Escandell, Alejandro
Ibañez-Cabellos, José Santiago
de Cutanda, Sergio Bañuls-Sánchez
Berenguer-Pascual, Ester
Beltrán-García, Jesús
García-López, Eva
Pallardó, Federico V.
García-Giménez, José Luis
Pallarés-Sabater, Antonio
Zarzosa-López, Ignacio
Monterde, Manuel
author_facet Victoria-Escandell, Alejandro
Ibañez-Cabellos, José Santiago
de Cutanda, Sergio Bañuls-Sánchez
Berenguer-Pascual, Ester
Beltrán-García, Jesús
García-López, Eva
Pallardó, Federico V.
García-Giménez, José Luis
Pallarés-Sabater, Antonio
Zarzosa-López, Ignacio
Monterde, Manuel
author_sort Victoria-Escandell, Alejandro
collection PubMed
description Human dental pulp stem cells (HDPSCs) are of special relevance in future regenerative dental therapies. Characterizing cytotoxicity and genotoxicity produced by endodontic materials is required to evaluate the potential for regeneration of injured tissues in future strategies combining regenerative and root canal therapies. This study explores the cytotoxicity and genotoxicity mediated by oxidative stress of three endodontic materials that are widely used on HDPSCs: a mineral trioxide aggregate (MTA-Angelus white), an epoxy resin sealant (AH-Plus cement), and an MTA-based cement sealer (MTA-Fillapex). Cell viability and cell death rate were assessed by flow cytometry. Oxidative stress was measured by OxyBlot. Levels of antioxidant enzymes were evaluated by Western blot. Genotoxicity was studied by quantifying the expression levels of DNA damage sensors such as ATM and RAD53 genes and DNA damage repair sensors such as RAD51 and PARP-1. Results indicate that AH-Plus increased apoptosis, oxidative stress, and genotoxicity markers in HDPSCs. MTA-Fillapex was the most cytotoxic oxidative stress inductor and genotoxic material for HDPSCs at longer times in preincubated cell culture medium, and MTA-Angelus was less cytotoxic and genotoxic than AH-Plus and MTA-Fillapex at all times assayed.
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spelling pubmed-55116672017-07-27 Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials Victoria-Escandell, Alejandro Ibañez-Cabellos, José Santiago de Cutanda, Sergio Bañuls-Sánchez Berenguer-Pascual, Ester Beltrán-García, Jesús García-López, Eva Pallardó, Federico V. García-Giménez, José Luis Pallarés-Sabater, Antonio Zarzosa-López, Ignacio Monterde, Manuel Stem Cells Int Research Article Human dental pulp stem cells (HDPSCs) are of special relevance in future regenerative dental therapies. Characterizing cytotoxicity and genotoxicity produced by endodontic materials is required to evaluate the potential for regeneration of injured tissues in future strategies combining regenerative and root canal therapies. This study explores the cytotoxicity and genotoxicity mediated by oxidative stress of three endodontic materials that are widely used on HDPSCs: a mineral trioxide aggregate (MTA-Angelus white), an epoxy resin sealant (AH-Plus cement), and an MTA-based cement sealer (MTA-Fillapex). Cell viability and cell death rate were assessed by flow cytometry. Oxidative stress was measured by OxyBlot. Levels of antioxidant enzymes were evaluated by Western blot. Genotoxicity was studied by quantifying the expression levels of DNA damage sensors such as ATM and RAD53 genes and DNA damage repair sensors such as RAD51 and PARP-1. Results indicate that AH-Plus increased apoptosis, oxidative stress, and genotoxicity markers in HDPSCs. MTA-Fillapex was the most cytotoxic oxidative stress inductor and genotoxic material for HDPSCs at longer times in preincubated cell culture medium, and MTA-Angelus was less cytotoxic and genotoxic than AH-Plus and MTA-Fillapex at all times assayed. Hindawi 2017 2017-05-24 /pmc/articles/PMC5511667/ /pubmed/28751918 http://dx.doi.org/10.1155/2017/8920356 Text en Copyright © 2017 Alejandro Victoria-Escandell 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
Victoria-Escandell, Alejandro
Ibañez-Cabellos, José Santiago
de Cutanda, Sergio Bañuls-Sánchez
Berenguer-Pascual, Ester
Beltrán-García, Jesús
García-López, Eva
Pallardó, Federico V.
García-Giménez, José Luis
Pallarés-Sabater, Antonio
Zarzosa-López, Ignacio
Monterde, Manuel
Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials
title Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials
title_full Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials
title_fullStr Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials
title_full_unstemmed Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials
title_short Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials
title_sort cellular responses in human dental pulp stem cells treated with three endodontic materials
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511667/
https://www.ncbi.nlm.nih.gov/pubmed/28751918
http://dx.doi.org/10.1155/2017/8920356
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