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Platelet-Rich Plasma Induces Autophagy and Promotes Regeneration in Human Dental Pulp Cells
Regenerative endodontic procedures using autologous platelet-rich plasma (PRP) can improve the biologic outcome of treatment. However, its mechanism of action on improving pulp regeneration is not fully elucidated. Autophagy was recently shown to be related to tissue repair and osteogenesis. Therefo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455824/ https://www.ncbi.nlm.nih.gov/pubmed/34568294 http://dx.doi.org/10.3389/fbioe.2021.659742 |
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author | Xu, Hanxin Xu, Fen Zhao, Jiajia Zhou, Caixia Liu, Jiarong |
author_facet | Xu, Hanxin Xu, Fen Zhao, Jiajia Zhou, Caixia Liu, Jiarong |
author_sort | Xu, Hanxin |
collection | PubMed |
description | Regenerative endodontic procedures using autologous platelet-rich plasma (PRP) can improve the biologic outcome of treatment. However, its mechanism of action on improving pulp regeneration is not fully elucidated. Autophagy was recently shown to be related to tissue repair and osteogenesis. Therefore, the objective of this study was to investigate the effect of PRP in dental pulp regeneration and to elucidate the role of autophagy involved in this process. Human dental pulp cells (hDPCs) were isolated from healthy dental pulp and co-cultured with an increasing concentration of PRP. Cellular migration and proliferation were determined by scratch assay, transwell assay, and cell-counting kit 8 assay. Osteogenic differentiation was clarified by using alkaline phosphatase staining, alizarin red staining, and real-time polymerase chain reaction (RT-PCR) to measure the gene expression levels of alkaline phosphatase, collagen-1, osteocalcin, dentin matrix protein 1, and dentin sialophosphoprotein. Autophagic bodies were observed by transmission electron microscopy and the expression of autophagy marker light chain 3B (LC3B) was determined by immunofluorescence staining. The mRNA and protein expression level of LC3B and Beclin-1 were quantified by qRT-PCR and western blotting. The effect of PRP on cellular migration, proliferation, and osteogenic differentiation was further investigated in the milieu of autophagy activator, rapamycin, and inhibitor, 3-methyladenine. Results showed that PRP promoted cell migration, proliferation, and osteogenic differentiation. Autophagic bodies were strongly activated and the expression level of LC3B and Beclin-1 was significantly promoted by PRP. Autophagy inhibition suppressed PRP-induced hDPCs migration, proliferation, and osteogenic differentiation, whereas autophagy activator substantially augmented PRP-stimulated migration, proliferation, and differentiation. Taken together, these findings suggested that PRP could effectively promote regenerative potentials associated with autophagy. |
format | Online Article Text |
id | pubmed-8455824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84558242021-09-23 Platelet-Rich Plasma Induces Autophagy and Promotes Regeneration in Human Dental Pulp Cells Xu, Hanxin Xu, Fen Zhao, Jiajia Zhou, Caixia Liu, Jiarong Front Bioeng Biotechnol Bioengineering and Biotechnology Regenerative endodontic procedures using autologous platelet-rich plasma (PRP) can improve the biologic outcome of treatment. However, its mechanism of action on improving pulp regeneration is not fully elucidated. Autophagy was recently shown to be related to tissue repair and osteogenesis. Therefore, the objective of this study was to investigate the effect of PRP in dental pulp regeneration and to elucidate the role of autophagy involved in this process. Human dental pulp cells (hDPCs) were isolated from healthy dental pulp and co-cultured with an increasing concentration of PRP. Cellular migration and proliferation were determined by scratch assay, transwell assay, and cell-counting kit 8 assay. Osteogenic differentiation was clarified by using alkaline phosphatase staining, alizarin red staining, and real-time polymerase chain reaction (RT-PCR) to measure the gene expression levels of alkaline phosphatase, collagen-1, osteocalcin, dentin matrix protein 1, and dentin sialophosphoprotein. Autophagic bodies were observed by transmission electron microscopy and the expression of autophagy marker light chain 3B (LC3B) was determined by immunofluorescence staining. The mRNA and protein expression level of LC3B and Beclin-1 were quantified by qRT-PCR and western blotting. The effect of PRP on cellular migration, proliferation, and osteogenic differentiation was further investigated in the milieu of autophagy activator, rapamycin, and inhibitor, 3-methyladenine. Results showed that PRP promoted cell migration, proliferation, and osteogenic differentiation. Autophagic bodies were strongly activated and the expression level of LC3B and Beclin-1 was significantly promoted by PRP. Autophagy inhibition suppressed PRP-induced hDPCs migration, proliferation, and osteogenic differentiation, whereas autophagy activator substantially augmented PRP-stimulated migration, proliferation, and differentiation. Taken together, these findings suggested that PRP could effectively promote regenerative potentials associated with autophagy. Frontiers Media S.A. 2021-09-08 /pmc/articles/PMC8455824/ /pubmed/34568294 http://dx.doi.org/10.3389/fbioe.2021.659742 Text en Copyright © 2021 Xu, Xu, Zhao, Zhou and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Xu, Hanxin Xu, Fen Zhao, Jiajia Zhou, Caixia Liu, Jiarong Platelet-Rich Plasma Induces Autophagy and Promotes Regeneration in Human Dental Pulp Cells |
title | Platelet-Rich Plasma Induces Autophagy and Promotes Regeneration in Human Dental Pulp Cells |
title_full | Platelet-Rich Plasma Induces Autophagy and Promotes Regeneration in Human Dental Pulp Cells |
title_fullStr | Platelet-Rich Plasma Induces Autophagy and Promotes Regeneration in Human Dental Pulp Cells |
title_full_unstemmed | Platelet-Rich Plasma Induces Autophagy and Promotes Regeneration in Human Dental Pulp Cells |
title_short | Platelet-Rich Plasma Induces Autophagy and Promotes Regeneration in Human Dental Pulp Cells |
title_sort | platelet-rich plasma induces autophagy and promotes regeneration in human dental pulp cells |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455824/ https://www.ncbi.nlm.nih.gov/pubmed/34568294 http://dx.doi.org/10.3389/fbioe.2021.659742 |
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