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Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis
The interaction between immune cells and stem cells is important during tissue repair. Macrophages have been described as being crucial for limb regeneration and in certain circumstances have been shown to affect stem cell differentiation in vivo. Dentine is susceptible to damage as a result of cari...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678850/ https://www.ncbi.nlm.nih.gov/pubmed/33214653 http://dx.doi.org/10.1038/s41598-020-77161-4 |
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author | Neves, Vitor C. M. Yianni, Val Sharpe, Paul T. |
author_facet | Neves, Vitor C. M. Yianni, Val Sharpe, Paul T. |
author_sort | Neves, Vitor C. M. |
collection | PubMed |
description | The interaction between immune cells and stem cells is important during tissue repair. Macrophages have been described as being crucial for limb regeneration and in certain circumstances have been shown to affect stem cell differentiation in vivo. Dentine is susceptible to damage as a result of caries, pulp infection and inflammation all of which are major problems in tooth restoration. Characterising the interplay between immune cells and stem cells is crucial to understand how to improve natural repair mechanisms. In this study, we used an in vivo damage model, associated with a macrophage and neutrophil depletion model to investigate the role of immune cells in reparative dentine formation. In addition, we investigated the effect of elevating the Wnt/β-catenin pathway to understand how this might regulate macrophages and impact upon Wnt receiving pulp stem cells during repair. Our results show that macrophages are required for dental pulp stem cell activation and appropriate reparative dentine formation. In addition, pharmacological stimulation of the Wnt/β-catenin pathway via GSK-3β inhibitor small molecules polarises macrophages to an anti-inflammatory state faster than inert calcium silicate-based materials thereby accelerating stem cell activation and repair. Wnt/β-catenin signalling thus has a dual role in promoting reparative dentine formation by activating pulp stem cells and promoting an anti-inflammatory macrophage response. |
format | Online Article Text |
id | pubmed-7678850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76788502020-11-23 Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis Neves, Vitor C. M. Yianni, Val Sharpe, Paul T. Sci Rep Article The interaction between immune cells and stem cells is important during tissue repair. Macrophages have been described as being crucial for limb regeneration and in certain circumstances have been shown to affect stem cell differentiation in vivo. Dentine is susceptible to damage as a result of caries, pulp infection and inflammation all of which are major problems in tooth restoration. Characterising the interplay between immune cells and stem cells is crucial to understand how to improve natural repair mechanisms. In this study, we used an in vivo damage model, associated with a macrophage and neutrophil depletion model to investigate the role of immune cells in reparative dentine formation. In addition, we investigated the effect of elevating the Wnt/β-catenin pathway to understand how this might regulate macrophages and impact upon Wnt receiving pulp stem cells during repair. Our results show that macrophages are required for dental pulp stem cell activation and appropriate reparative dentine formation. In addition, pharmacological stimulation of the Wnt/β-catenin pathway via GSK-3β inhibitor small molecules polarises macrophages to an anti-inflammatory state faster than inert calcium silicate-based materials thereby accelerating stem cell activation and repair. Wnt/β-catenin signalling thus has a dual role in promoting reparative dentine formation by activating pulp stem cells and promoting an anti-inflammatory macrophage response. Nature Publishing Group UK 2020-11-19 /pmc/articles/PMC7678850/ /pubmed/33214653 http://dx.doi.org/10.1038/s41598-020-77161-4 Text en © The Author(s) 2020 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 Neves, Vitor C. M. Yianni, Val Sharpe, Paul T. Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis |
title | Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis |
title_full | Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis |
title_fullStr | Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis |
title_full_unstemmed | Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis |
title_short | Macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis |
title_sort | macrophage modulation of dental pulp stem cell activity during tertiary dentinogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678850/ https://www.ncbi.nlm.nih.gov/pubmed/33214653 http://dx.doi.org/10.1038/s41598-020-77161-4 |
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