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Berberine-releasing electrospun scaffold induces osteogenic differentiation of DPSCs and accelerates bone repair

The repair of skeletal defects in maxillofacial region remains an intractable problem, the rising technology of bone tissue engineering provides a new strategy to solve it. Scaffolds, a crucial element of tissue engineering, must have favorable biocompatibility as well as osteoinductivity. In this s...

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Autores principales: Ma, Lan, Yu, Yijun, Liu, Hanxiao, Sun, Weibin, Lin, Zitong, Liu, Chao, Miao, Leiying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806735/
https://www.ncbi.nlm.nih.gov/pubmed/33441759
http://dx.doi.org/10.1038/s41598-020-79734-9
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author Ma, Lan
Yu, Yijun
Liu, Hanxiao
Sun, Weibin
Lin, Zitong
Liu, Chao
Miao, Leiying
author_facet Ma, Lan
Yu, Yijun
Liu, Hanxiao
Sun, Weibin
Lin, Zitong
Liu, Chao
Miao, Leiying
author_sort Ma, Lan
collection PubMed
description The repair of skeletal defects in maxillofacial region remains an intractable problem, the rising technology of bone tissue engineering provides a new strategy to solve it. Scaffolds, a crucial element of tissue engineering, must have favorable biocompatibility as well as osteoinductivity. In this study, we prepared berberine/polycaprolactone/collagen (BBR/PCL/COL) scaffolds with different concentrations of berberine (BBR) (25, 50, 75 and 100 μg/mL) through electrospinning. The influence of dosage on scaffold morphology, cell behavior and in vivo bone defect repair were systematically studied. The results indicated that scaffolds could release BBR stably for up to 27 days. Experiments in vitro showed that BBR/PCL/COL scaffolds had appropriate biocompatibility in the concentration of 25–75 μg/mL, and 50 and 75 μg/mL scaffolds could significantly promote osteogenic differentiation of dental pulp stem cells. Scaffold with 50 μg/mL BBR was implanted into the critical bone defect of rats to evaluate the ability of bone repair in vivo. It was found that BBR/PCL/COL scaffold performed more favorable than polycaprolactone/collagen (PCL/COL) scaffold. Overall, our study is the first to evaluate the capability of in vivo bone repair of BBR/PCL/COL electrospun scaffold. The results indicate that BBR/PCL/COL scaffold has prospective potential for tissue engineering applications in bone regeneration therapy.
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spelling pubmed-78067352021-01-14 Berberine-releasing electrospun scaffold induces osteogenic differentiation of DPSCs and accelerates bone repair Ma, Lan Yu, Yijun Liu, Hanxiao Sun, Weibin Lin, Zitong Liu, Chao Miao, Leiying Sci Rep Article The repair of skeletal defects in maxillofacial region remains an intractable problem, the rising technology of bone tissue engineering provides a new strategy to solve it. Scaffolds, a crucial element of tissue engineering, must have favorable biocompatibility as well as osteoinductivity. In this study, we prepared berberine/polycaprolactone/collagen (BBR/PCL/COL) scaffolds with different concentrations of berberine (BBR) (25, 50, 75 and 100 μg/mL) through electrospinning. The influence of dosage on scaffold morphology, cell behavior and in vivo bone defect repair were systematically studied. The results indicated that scaffolds could release BBR stably for up to 27 days. Experiments in vitro showed that BBR/PCL/COL scaffolds had appropriate biocompatibility in the concentration of 25–75 μg/mL, and 50 and 75 μg/mL scaffolds could significantly promote osteogenic differentiation of dental pulp stem cells. Scaffold with 50 μg/mL BBR was implanted into the critical bone defect of rats to evaluate the ability of bone repair in vivo. It was found that BBR/PCL/COL scaffold performed more favorable than polycaprolactone/collagen (PCL/COL) scaffold. Overall, our study is the first to evaluate the capability of in vivo bone repair of BBR/PCL/COL electrospun scaffold. The results indicate that BBR/PCL/COL scaffold has prospective potential for tissue engineering applications in bone regeneration therapy. Nature Publishing Group UK 2021-01-13 /pmc/articles/PMC7806735/ /pubmed/33441759 http://dx.doi.org/10.1038/s41598-020-79734-9 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ma, Lan
Yu, Yijun
Liu, Hanxiao
Sun, Weibin
Lin, Zitong
Liu, Chao
Miao, Leiying
Berberine-releasing electrospun scaffold induces osteogenic differentiation of DPSCs and accelerates bone repair
title Berberine-releasing electrospun scaffold induces osteogenic differentiation of DPSCs and accelerates bone repair
title_full Berberine-releasing electrospun scaffold induces osteogenic differentiation of DPSCs and accelerates bone repair
title_fullStr Berberine-releasing electrospun scaffold induces osteogenic differentiation of DPSCs and accelerates bone repair
title_full_unstemmed Berberine-releasing electrospun scaffold induces osteogenic differentiation of DPSCs and accelerates bone repair
title_short Berberine-releasing electrospun scaffold induces osteogenic differentiation of DPSCs and accelerates bone repair
title_sort berberine-releasing electrospun scaffold induces osteogenic differentiation of dpscs and accelerates bone repair
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806735/
https://www.ncbi.nlm.nih.gov/pubmed/33441759
http://dx.doi.org/10.1038/s41598-020-79734-9
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