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Role of osteopontin in the process of pulpal healing following tooth replantation in mice
INTRODUCTION: The role of osteopontin (OPN) following severe injury remains to be elucidated, especially its relationship with type I collagen (encoded by the Col1a1 gene) secretion by newly-differentiated odontoblast-like cells (OBLCs). In this study, we examined the role of OPN in the process of r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Society for Regenerative Medicine
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587125/ https://www.ncbi.nlm.nih.gov/pubmed/36313391 http://dx.doi.org/10.1016/j.reth.2022.09.011 |
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author | Suzuki-Barrera, Kiyoko Makishi, Sanako Nakatomi, Mitsushiro Saito, Kotaro Ida-Yonemochi, Hiroko Ohshima, Hayato |
author_facet | Suzuki-Barrera, Kiyoko Makishi, Sanako Nakatomi, Mitsushiro Saito, Kotaro Ida-Yonemochi, Hiroko Ohshima, Hayato |
author_sort | Suzuki-Barrera, Kiyoko |
collection | PubMed |
description | INTRODUCTION: The role of osteopontin (OPN) following severe injury remains to be elucidated, especially its relationship with type I collagen (encoded by the Col1a1 gene) secretion by newly-differentiated odontoblast-like cells (OBLCs). In this study, we examined the role of OPN in the process of reparative dentin formation with a focus on reinnervation and revascularization after tooth replantation in Opn knockout (KO) and wild-type (WT) mice. METHODS: Maxillary first molars of 2- and 3-week-old-Opn KO and WT mice (Opn KO 2W, Opn KO 3W, WT 2W, and WT 3W groups) were replanted, followed by fixation 3–56 days after operation. Following micro-computed tomography analysis, the decalcified samples were processed for immunohistochemistry for Ki67, Nestin, PGP 9.5, and CD31 and in situ hybridization for Col1a1. RESULTS: An intense inflammatory reaction occurred to disrupt pulpal healing in the replanted teeth of the Opn KO 3W group, whereas dental pulp achieved healing in the Opn KO 2W and WT groups. The tertiary dentin in the Opn KO 3W group was significantly decreased in area compared with the Opn KO 2W and WT groups, with a significantly low percentage of Nestin-positive, newly-differentiated OBLCs during postoperative days 7–14. In the Opn KO 3W group, the blood vessels were significantly decreased in area and pulp healing was disturbed with a failure of pulpal revascularization and reinnervation. CONCLUSIONS: OPN is necessary for proper reinnervation and revascularization to deposit reparative dentin following severe injury within the dental pulp of erupted teeth with advanced root development. |
format | Online Article Text |
id | pubmed-9587125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Japanese Society for Regenerative Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-95871252022-10-27 Role of osteopontin in the process of pulpal healing following tooth replantation in mice Suzuki-Barrera, Kiyoko Makishi, Sanako Nakatomi, Mitsushiro Saito, Kotaro Ida-Yonemochi, Hiroko Ohshima, Hayato Regen Ther Original Article INTRODUCTION: The role of osteopontin (OPN) following severe injury remains to be elucidated, especially its relationship with type I collagen (encoded by the Col1a1 gene) secretion by newly-differentiated odontoblast-like cells (OBLCs). In this study, we examined the role of OPN in the process of reparative dentin formation with a focus on reinnervation and revascularization after tooth replantation in Opn knockout (KO) and wild-type (WT) mice. METHODS: Maxillary first molars of 2- and 3-week-old-Opn KO and WT mice (Opn KO 2W, Opn KO 3W, WT 2W, and WT 3W groups) were replanted, followed by fixation 3–56 days after operation. Following micro-computed tomography analysis, the decalcified samples were processed for immunohistochemistry for Ki67, Nestin, PGP 9.5, and CD31 and in situ hybridization for Col1a1. RESULTS: An intense inflammatory reaction occurred to disrupt pulpal healing in the replanted teeth of the Opn KO 3W group, whereas dental pulp achieved healing in the Opn KO 2W and WT groups. The tertiary dentin in the Opn KO 3W group was significantly decreased in area compared with the Opn KO 2W and WT groups, with a significantly low percentage of Nestin-positive, newly-differentiated OBLCs during postoperative days 7–14. In the Opn KO 3W group, the blood vessels were significantly decreased in area and pulp healing was disturbed with a failure of pulpal revascularization and reinnervation. CONCLUSIONS: OPN is necessary for proper reinnervation and revascularization to deposit reparative dentin following severe injury within the dental pulp of erupted teeth with advanced root development. Japanese Society for Regenerative Medicine 2022-10-18 /pmc/articles/PMC9587125/ /pubmed/36313391 http://dx.doi.org/10.1016/j.reth.2022.09.011 Text en © 2022 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Suzuki-Barrera, Kiyoko Makishi, Sanako Nakatomi, Mitsushiro Saito, Kotaro Ida-Yonemochi, Hiroko Ohshima, Hayato Role of osteopontin in the process of pulpal healing following tooth replantation in mice |
title | Role of osteopontin in the process of pulpal healing following tooth replantation in mice |
title_full | Role of osteopontin in the process of pulpal healing following tooth replantation in mice |
title_fullStr | Role of osteopontin in the process of pulpal healing following tooth replantation in mice |
title_full_unstemmed | Role of osteopontin in the process of pulpal healing following tooth replantation in mice |
title_short | Role of osteopontin in the process of pulpal healing following tooth replantation in mice |
title_sort | role of osteopontin in the process of pulpal healing following tooth replantation in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587125/ https://www.ncbi.nlm.nih.gov/pubmed/36313391 http://dx.doi.org/10.1016/j.reth.2022.09.011 |
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