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Biocompatibility of Biodentine™ (®) with Periodontal Ligament Stem Cells: In Vitro Study

Biodentine™ is a tricalcium silicate-based cement material that has a great impact on different biological processes of dental stem cells, compared to other biomaterials. Therefore, we aimed to investigate the optimum biocompatible concentration of Biodentine™ with stem cells derived from periodonta...

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Autores principales: Abuarqoub, Duaa, Aslam, Nazneen, Jafar, Hanan, Abu Harfil, Zakariya, Awidi, Abdalla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148534/
https://www.ncbi.nlm.nih.gov/pubmed/32046292
http://dx.doi.org/10.3390/dj8010017
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author Abuarqoub, Duaa
Aslam, Nazneen
Jafar, Hanan
Abu Harfil, Zakariya
Awidi, Abdalla
author_facet Abuarqoub, Duaa
Aslam, Nazneen
Jafar, Hanan
Abu Harfil, Zakariya
Awidi, Abdalla
author_sort Abuarqoub, Duaa
collection PubMed
description Biodentine™ is a tricalcium silicate-based cement material that has a great impact on different biological processes of dental stem cells, compared to other biomaterials. Therefore, we aimed to investigate the optimum biocompatible concentration of Biodentine™ with stem cells derived from periodontal ligament (hPDLSCs) by determining cell proliferation, cytotoxicity, migration, adhesion and mineralization potential. hPDLSCs were treated with Biodentine™ extract at different concentrations; 20, 2, 0.2 and 0.02 mg/mL. Cells cultured without Biodentine™ were used as a blank control. The proliferation potential of hPDLSCs was evaluated by MTT viability analysis for 6 days. Cytotoxicity assay was performed after 3 days by using AnnexinV/7AAD. Migration potential was investigated by wound healing and transwell migration assays at both cellular and molecular levels. The expression levels of chemokines CXCR4, MCP-1 and adhesion molecules FGF-2, FN, VCAM and ICAM-1 were measured by qPCR. The communication potentials of these cells were determined by adhesion assay. In addition, mineralization potential was evaluated by measuring the expression levels of osteogenic markers; ALP, OCN, OPN and Collagen type1 by qPCR. Our results showed significant increase in the proliferation of hPDLSCs at low concentrations of Biodentine™ (2, 0.2 and 0.02 mg/mL) while higher concentration (20 mg/mL) exhibited cytotoxic effect on the cells. Moreover, 2 mg/mL Biodentine™ showed a significant increase in the migration, adhesion and mineralization potentials of the derived cells among all concentrations and when compared to the blank control. Our findings suggest that 2 mg/mL of Biodentine™ is the most biocompatible concentration with hPDLSCs, showing a high stimulatory effect on the biological processes.
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spelling pubmed-71485342020-04-20 Biocompatibility of Biodentine™ (®) with Periodontal Ligament Stem Cells: In Vitro Study Abuarqoub, Duaa Aslam, Nazneen Jafar, Hanan Abu Harfil, Zakariya Awidi, Abdalla Dent J (Basel) Article Biodentine™ is a tricalcium silicate-based cement material that has a great impact on different biological processes of dental stem cells, compared to other biomaterials. Therefore, we aimed to investigate the optimum biocompatible concentration of Biodentine™ with stem cells derived from periodontal ligament (hPDLSCs) by determining cell proliferation, cytotoxicity, migration, adhesion and mineralization potential. hPDLSCs were treated with Biodentine™ extract at different concentrations; 20, 2, 0.2 and 0.02 mg/mL. Cells cultured without Biodentine™ were used as a blank control. The proliferation potential of hPDLSCs was evaluated by MTT viability analysis for 6 days. Cytotoxicity assay was performed after 3 days by using AnnexinV/7AAD. Migration potential was investigated by wound healing and transwell migration assays at both cellular and molecular levels. The expression levels of chemokines CXCR4, MCP-1 and adhesion molecules FGF-2, FN, VCAM and ICAM-1 were measured by qPCR. The communication potentials of these cells were determined by adhesion assay. In addition, mineralization potential was evaluated by measuring the expression levels of osteogenic markers; ALP, OCN, OPN and Collagen type1 by qPCR. Our results showed significant increase in the proliferation of hPDLSCs at low concentrations of Biodentine™ (2, 0.2 and 0.02 mg/mL) while higher concentration (20 mg/mL) exhibited cytotoxic effect on the cells. Moreover, 2 mg/mL Biodentine™ showed a significant increase in the migration, adhesion and mineralization potentials of the derived cells among all concentrations and when compared to the blank control. Our findings suggest that 2 mg/mL of Biodentine™ is the most biocompatible concentration with hPDLSCs, showing a high stimulatory effect on the biological processes. MDPI 2020-02-08 /pmc/articles/PMC7148534/ /pubmed/32046292 http://dx.doi.org/10.3390/dj8010017 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abuarqoub, Duaa
Aslam, Nazneen
Jafar, Hanan
Abu Harfil, Zakariya
Awidi, Abdalla
Biocompatibility of Biodentine™ (®) with Periodontal Ligament Stem Cells: In Vitro Study
title Biocompatibility of Biodentine™ (®) with Periodontal Ligament Stem Cells: In Vitro Study
title_full Biocompatibility of Biodentine™ (®) with Periodontal Ligament Stem Cells: In Vitro Study
title_fullStr Biocompatibility of Biodentine™ (®) with Periodontal Ligament Stem Cells: In Vitro Study
title_full_unstemmed Biocompatibility of Biodentine™ (®) with Periodontal Ligament Stem Cells: In Vitro Study
title_short Biocompatibility of Biodentine™ (®) with Periodontal Ligament Stem Cells: In Vitro Study
title_sort biocompatibility of biodentine™ (®) with periodontal ligament stem cells: in vitro study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148534/
https://www.ncbi.nlm.nih.gov/pubmed/32046292
http://dx.doi.org/10.3390/dj8010017
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