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Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold

Poly(l-lactide-co-caprolactone) (PLCL) electrospun scaffolds with seeded stem cells have drawn great interest in tissue engineering. This study investigated the biological behavior of human dental pulp stem cells (hDPSCs) grown on a hydrolytically-modified PLCL nanofiber scaffold. The hDPSCs were se...

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Autores principales: Bar, Julia K., Kowalczyk, Tomasz, Grelewski, Piotr G., Stamnitz, Sandra, Paprocka, Maria, Lis, Joanna, Lis-Nawara, Anna, An, Seongpil, Klimczak, Aleksandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911644/
https://www.ncbi.nlm.nih.gov/pubmed/35269131
http://dx.doi.org/10.3390/ma15051900
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author Bar, Julia K.
Kowalczyk, Tomasz
Grelewski, Piotr G.
Stamnitz, Sandra
Paprocka, Maria
Lis, Joanna
Lis-Nawara, Anna
An, Seongpil
Klimczak, Aleksandra
author_facet Bar, Julia K.
Kowalczyk, Tomasz
Grelewski, Piotr G.
Stamnitz, Sandra
Paprocka, Maria
Lis, Joanna
Lis-Nawara, Anna
An, Seongpil
Klimczak, Aleksandra
author_sort Bar, Julia K.
collection PubMed
description Poly(l-lactide-co-caprolactone) (PLCL) electrospun scaffolds with seeded stem cells have drawn great interest in tissue engineering. This study investigated the biological behavior of human dental pulp stem cells (hDPSCs) grown on a hydrolytically-modified PLCL nanofiber scaffold. The hDPSCs were seeded on PLCL, and their biological features such as viability, proliferation, adhesion, population doubling time, the immunophenotype of hDPSCs and osteogenic differentiation capacity were evaluated on scaffolds. The results showed that the PLCL scaffold significantly supported hDPSC viability/proliferation. The hDPSCs adhesion rate and spreading onto PLCL increased with time of culture. hDPSCs were able to migrate inside the PLCL electrospun scaffold after 7 days of seeding. No differences in morphology and immunophenotype of hDPSCs grown on PLCL and in flasks were observed. The mRNA levels of bone-related genes and their proteins were significantly higher in hDPSCs after osteogenic differentiation on PLCL compared with undifferentiated hDPSCs on PLCL. These results showed that the mechanical properties of a modified PLCL mat provide an appropriate environment that supports hDPSCs attachment, proliferation, migration and their osteogenic differentiation on the PLCL scaffold. The good PLCL biocompatibility with dental pulp stem cells indicates that this mat may be applied in designing a bioactive hDPSCs/PLCL construct for bone tissue engineering.
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spelling pubmed-89116442022-03-11 Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold Bar, Julia K. Kowalczyk, Tomasz Grelewski, Piotr G. Stamnitz, Sandra Paprocka, Maria Lis, Joanna Lis-Nawara, Anna An, Seongpil Klimczak, Aleksandra Materials (Basel) Article Poly(l-lactide-co-caprolactone) (PLCL) electrospun scaffolds with seeded stem cells have drawn great interest in tissue engineering. This study investigated the biological behavior of human dental pulp stem cells (hDPSCs) grown on a hydrolytically-modified PLCL nanofiber scaffold. The hDPSCs were seeded on PLCL, and their biological features such as viability, proliferation, adhesion, population doubling time, the immunophenotype of hDPSCs and osteogenic differentiation capacity were evaluated on scaffolds. The results showed that the PLCL scaffold significantly supported hDPSC viability/proliferation. The hDPSCs adhesion rate and spreading onto PLCL increased with time of culture. hDPSCs were able to migrate inside the PLCL electrospun scaffold after 7 days of seeding. No differences in morphology and immunophenotype of hDPSCs grown on PLCL and in flasks were observed. The mRNA levels of bone-related genes and their proteins were significantly higher in hDPSCs after osteogenic differentiation on PLCL compared with undifferentiated hDPSCs on PLCL. These results showed that the mechanical properties of a modified PLCL mat provide an appropriate environment that supports hDPSCs attachment, proliferation, migration and their osteogenic differentiation on the PLCL scaffold. The good PLCL biocompatibility with dental pulp stem cells indicates that this mat may be applied in designing a bioactive hDPSCs/PLCL construct for bone tissue engineering. MDPI 2022-03-03 /pmc/articles/PMC8911644/ /pubmed/35269131 http://dx.doi.org/10.3390/ma15051900 Text en © 2022 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
Bar, Julia K.
Kowalczyk, Tomasz
Grelewski, Piotr G.
Stamnitz, Sandra
Paprocka, Maria
Lis, Joanna
Lis-Nawara, Anna
An, Seongpil
Klimczak, Aleksandra
Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold
title Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold
title_full Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold
title_fullStr Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold
title_full_unstemmed Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold
title_short Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold
title_sort characterization of biological properties of dental pulp stem cells grown on an electrospun poly(l-lactide-co-caprolactone) scaffold
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911644/
https://www.ncbi.nlm.nih.gov/pubmed/35269131
http://dx.doi.org/10.3390/ma15051900
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