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Npp1 prevents external tooth root resorption by regulation of cervical cementum integrity
Tooth roots embedded in the alveolar bone do not typically undergo resorption while the bone continues remodeling in its physiological state. In this study, we analyzed genetically modified mice with the functional inactivation of nucleotide pyrophosphatase 1 (Npp1), encoded by ectonucleotide pyroph...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729310/ https://www.ncbi.nlm.nih.gov/pubmed/36477209 http://dx.doi.org/10.1038/s41598-022-25846-3 |
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author | Choi, Hwajung Yang, Liu Liu, Yudong Jeong, Ju-Kyung Cho, Eui-Sic |
author_facet | Choi, Hwajung Yang, Liu Liu, Yudong Jeong, Ju-Kyung Cho, Eui-Sic |
author_sort | Choi, Hwajung |
collection | PubMed |
description | Tooth roots embedded in the alveolar bone do not typically undergo resorption while the bone continues remodeling in its physiological state. In this study, we analyzed genetically modified mice with the functional inactivation of nucleotide pyrophosphatase 1 (Npp1), encoded by ectonucleotide pyrophosphatase/phosphodiesterase 1 (Enpp1). This mutation leads to the formation of ectopic cervical cementum vulnerable to external tooth root resorption. Cementoblasts with the inactivation of Enpp1 extensively expressed non-collagenous matrix proteins enriched with bone sialoprotein (Bsp), dentin matrix protein 1 (Dmp1), and osteopontin (Opn), which have roles in mineralization through nucleation and in cell adhesion through the Arg-Gly-Asp (RGD) motif. In cementoblasts with the inactivation of Enpp1, β-catenin was significantly activated and induced the expression of these non-collagenous matrix proteins. In addition, adenosine triphosphate (ATP), which is the most preferred substrate of Npp1, accumulated extracellularly and autocrinally induced the expression of the receptor activator of nuclear factor κB ligand (Rankl) in cementoblasts with inactivated Npp1. Consequently, these results strongly suggest that functional Npp1 preserves cervical cementum integrity and supports the anti-resorptive properties of tooth roots through ATP homeostasis in the physiological state of cervical cementum. |
format | Online Article Text |
id | pubmed-9729310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97293102022-12-09 Npp1 prevents external tooth root resorption by regulation of cervical cementum integrity Choi, Hwajung Yang, Liu Liu, Yudong Jeong, Ju-Kyung Cho, Eui-Sic Sci Rep Article Tooth roots embedded in the alveolar bone do not typically undergo resorption while the bone continues remodeling in its physiological state. In this study, we analyzed genetically modified mice with the functional inactivation of nucleotide pyrophosphatase 1 (Npp1), encoded by ectonucleotide pyrophosphatase/phosphodiesterase 1 (Enpp1). This mutation leads to the formation of ectopic cervical cementum vulnerable to external tooth root resorption. Cementoblasts with the inactivation of Enpp1 extensively expressed non-collagenous matrix proteins enriched with bone sialoprotein (Bsp), dentin matrix protein 1 (Dmp1), and osteopontin (Opn), which have roles in mineralization through nucleation and in cell adhesion through the Arg-Gly-Asp (RGD) motif. In cementoblasts with the inactivation of Enpp1, β-catenin was significantly activated and induced the expression of these non-collagenous matrix proteins. In addition, adenosine triphosphate (ATP), which is the most preferred substrate of Npp1, accumulated extracellularly and autocrinally induced the expression of the receptor activator of nuclear factor κB ligand (Rankl) in cementoblasts with inactivated Npp1. Consequently, these results strongly suggest that functional Npp1 preserves cervical cementum integrity and supports the anti-resorptive properties of tooth roots through ATP homeostasis in the physiological state of cervical cementum. Nature Publishing Group UK 2022-12-07 /pmc/articles/PMC9729310/ /pubmed/36477209 http://dx.doi.org/10.1038/s41598-022-25846-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Choi, Hwajung Yang, Liu Liu, Yudong Jeong, Ju-Kyung Cho, Eui-Sic Npp1 prevents external tooth root resorption by regulation of cervical cementum integrity |
title | Npp1 prevents external tooth root resorption by regulation of cervical cementum integrity |
title_full | Npp1 prevents external tooth root resorption by regulation of cervical cementum integrity |
title_fullStr | Npp1 prevents external tooth root resorption by regulation of cervical cementum integrity |
title_full_unstemmed | Npp1 prevents external tooth root resorption by regulation of cervical cementum integrity |
title_short | Npp1 prevents external tooth root resorption by regulation of cervical cementum integrity |
title_sort | npp1 prevents external tooth root resorption by regulation of cervical cementum integrity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729310/ https://www.ncbi.nlm.nih.gov/pubmed/36477209 http://dx.doi.org/10.1038/s41598-022-25846-3 |
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