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Direct-Writing Electrospun Functionalized Scaffolds for Periodontal Regeneration: In Vitro Studies
Multiphasic scaffolds that combine different architectural, physical, and biological properties are the best option for the regeneration of complex tissues such as the periodontium. Current developed scaffolds generally lack architectural accuracy and rely on multistep manufacturing, which is diffic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218971/ https://www.ncbi.nlm.nih.gov/pubmed/37233373 http://dx.doi.org/10.3390/jfb14050263 |
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author | Bourdon, Laura Attik, Nina Belkessam, Liza Chevalier, Charlène Bousige, Colin Brioude, Arnaud Salles, Vincent |
author_facet | Bourdon, Laura Attik, Nina Belkessam, Liza Chevalier, Charlène Bousige, Colin Brioude, Arnaud Salles, Vincent |
author_sort | Bourdon, Laura |
collection | PubMed |
description | Multiphasic scaffolds that combine different architectural, physical, and biological properties are the best option for the regeneration of complex tissues such as the periodontium. Current developed scaffolds generally lack architectural accuracy and rely on multistep manufacturing, which is difficult to implement for clinical applications. In this context, direct-writing electrospinning (DWE) represents a promising and rapid technique for developing thin 3D scaffolds with controlled architecture. The current study aimed to elaborate a biphasic scaffold using DWE based on two polycaprolactone solutions with interesting properties for bone and cement regeneration. One of the two scaffold parts contained hydroxyapatite nanoparticles (HAP) and the other contained the cementum protein 1 (CEMP1). After morphological characterizations, the elaborated scaffolds were assessed regarding periodontal ligament (PDL) cells in terms of cell proliferation, colonization, and mineralization ability. The results demonstrated that both HAP- and CEMP1-functionalized scaffolds were colonized by PDL cells and enhanced mineralization ability compared to unfunctionalized scaffolds, as revealed by alizarin red staining and OPN protein fluorescent expression. Taken together, the current data highlighted the potential of functional and organized scaffolds to stimulate bone and cementum regeneration. Moreover, DWE could be used to develop smart scaffolds with the ability to spatially control cellular orientation with suitable cellular activity at the micrometer scale, thereby enhancing periodontal and other complex tissue regeneration. |
format | Online Article Text |
id | pubmed-10218971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102189712023-05-27 Direct-Writing Electrospun Functionalized Scaffolds for Periodontal Regeneration: In Vitro Studies Bourdon, Laura Attik, Nina Belkessam, Liza Chevalier, Charlène Bousige, Colin Brioude, Arnaud Salles, Vincent J Funct Biomater Article Multiphasic scaffolds that combine different architectural, physical, and biological properties are the best option for the regeneration of complex tissues such as the periodontium. Current developed scaffolds generally lack architectural accuracy and rely on multistep manufacturing, which is difficult to implement for clinical applications. In this context, direct-writing electrospinning (DWE) represents a promising and rapid technique for developing thin 3D scaffolds with controlled architecture. The current study aimed to elaborate a biphasic scaffold using DWE based on two polycaprolactone solutions with interesting properties for bone and cement regeneration. One of the two scaffold parts contained hydroxyapatite nanoparticles (HAP) and the other contained the cementum protein 1 (CEMP1). After morphological characterizations, the elaborated scaffolds were assessed regarding periodontal ligament (PDL) cells in terms of cell proliferation, colonization, and mineralization ability. The results demonstrated that both HAP- and CEMP1-functionalized scaffolds were colonized by PDL cells and enhanced mineralization ability compared to unfunctionalized scaffolds, as revealed by alizarin red staining and OPN protein fluorescent expression. Taken together, the current data highlighted the potential of functional and organized scaffolds to stimulate bone and cementum regeneration. Moreover, DWE could be used to develop smart scaffolds with the ability to spatially control cellular orientation with suitable cellular activity at the micrometer scale, thereby enhancing periodontal and other complex tissue regeneration. MDPI 2023-05-09 /pmc/articles/PMC10218971/ /pubmed/37233373 http://dx.doi.org/10.3390/jfb14050263 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bourdon, Laura Attik, Nina Belkessam, Liza Chevalier, Charlène Bousige, Colin Brioude, Arnaud Salles, Vincent Direct-Writing Electrospun Functionalized Scaffolds for Periodontal Regeneration: In Vitro Studies |
title | Direct-Writing Electrospun Functionalized Scaffolds for Periodontal Regeneration: In Vitro Studies |
title_full | Direct-Writing Electrospun Functionalized Scaffolds for Periodontal Regeneration: In Vitro Studies |
title_fullStr | Direct-Writing Electrospun Functionalized Scaffolds for Periodontal Regeneration: In Vitro Studies |
title_full_unstemmed | Direct-Writing Electrospun Functionalized Scaffolds for Periodontal Regeneration: In Vitro Studies |
title_short | Direct-Writing Electrospun Functionalized Scaffolds for Periodontal Regeneration: In Vitro Studies |
title_sort | direct-writing electrospun functionalized scaffolds for periodontal regeneration: in vitro studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218971/ https://www.ncbi.nlm.nih.gov/pubmed/37233373 http://dx.doi.org/10.3390/jfb14050263 |
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