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Dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases
Dentin is primarily composed of hydroxyapatite crystals within a rich organic matrix. The organic matrix comprises collagenous structural components, within which a variety of bioactive molecules are sequestered. During caries progression, dentin is degraded by acids and enzymes derived from various...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048071/ https://www.ncbi.nlm.nih.gov/pubmed/30013085 http://dx.doi.org/10.1038/s41598-018-29112-3 |
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author | Okamoto, Motoki Takahashi, Yusuke Komichi, Shungo Cooper, Paul R. Hayashi, Mikako |
author_facet | Okamoto, Motoki Takahashi, Yusuke Komichi, Shungo Cooper, Paul R. Hayashi, Mikako |
author_sort | Okamoto, Motoki |
collection | PubMed |
description | Dentin is primarily composed of hydroxyapatite crystals within a rich organic matrix. The organic matrix comprises collagenous structural components, within which a variety of bioactive molecules are sequestered. During caries progression, dentin is degraded by acids and enzymes derived from various sources, which can release bioactive molecules with potential reparative activity towards the dentin-pulp complex. While these molecules’ repair activities in other tissues are already known, their biological effects are unclear in relation to degradation events during disease in the dentin-pulp complex. This study was undertaken to investigate the effects of dentin matrix components (DMCs) that are partially digested by matrix metalloproteinases (MMPs) in vitro and in vivo during wound healing of the dentin-pulp complex. DMCs were initially isolated from healthy dentin and treated with recombinant MMPs. Subsequently, their effects on the behaviour of primary pulp cells were investigated in vitro and in vivo. Digested DMCs modulated a range of pulp cell functions in vitro. In addition, DMCs partially digested with MMP-20 stimulated tertiary dentin formation in vivo, which exhibited a more regular tubular structure than that induced by treatment with other MMPs. Our results indicate that MMP-20 may be especially effective in stimulating wound healing of the dentin-pulp complex. |
format | Online Article Text |
id | pubmed-6048071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60480712018-07-19 Dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases Okamoto, Motoki Takahashi, Yusuke Komichi, Shungo Cooper, Paul R. Hayashi, Mikako Sci Rep Article Dentin is primarily composed of hydroxyapatite crystals within a rich organic matrix. The organic matrix comprises collagenous structural components, within which a variety of bioactive molecules are sequestered. During caries progression, dentin is degraded by acids and enzymes derived from various sources, which can release bioactive molecules with potential reparative activity towards the dentin-pulp complex. While these molecules’ repair activities in other tissues are already known, their biological effects are unclear in relation to degradation events during disease in the dentin-pulp complex. This study was undertaken to investigate the effects of dentin matrix components (DMCs) that are partially digested by matrix metalloproteinases (MMPs) in vitro and in vivo during wound healing of the dentin-pulp complex. DMCs were initially isolated from healthy dentin and treated with recombinant MMPs. Subsequently, their effects on the behaviour of primary pulp cells were investigated in vitro and in vivo. Digested DMCs modulated a range of pulp cell functions in vitro. In addition, DMCs partially digested with MMP-20 stimulated tertiary dentin formation in vivo, which exhibited a more regular tubular structure than that induced by treatment with other MMPs. Our results indicate that MMP-20 may be especially effective in stimulating wound healing of the dentin-pulp complex. Nature Publishing Group UK 2018-07-16 /pmc/articles/PMC6048071/ /pubmed/30013085 http://dx.doi.org/10.1038/s41598-018-29112-3 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Okamoto, Motoki Takahashi, Yusuke Komichi, Shungo Cooper, Paul R. Hayashi, Mikako Dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases |
title | Dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases |
title_full | Dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases |
title_fullStr | Dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases |
title_full_unstemmed | Dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases |
title_short | Dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases |
title_sort | dentinogenic effects of extracted dentin matrix components digested with matrix metalloproteinases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048071/ https://www.ncbi.nlm.nih.gov/pubmed/30013085 http://dx.doi.org/10.1038/s41598-018-29112-3 |
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