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Development of a mouse model for pulp-dentin complex regeneration research: a preliminary study
OBJECTIVES: To achieve pulp-dentin complex regeneration with tissue engineering, treatment efficacies and safeties should be evaluated using in vivo orthotopic transplantation in a sufficient number of animals. Mice have been a species of choice in which to study stem cell biology in mammals. Howeve...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Conservative Dentistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529795/ https://www.ncbi.nlm.nih.gov/pubmed/31149618 http://dx.doi.org/10.5395/rde.2019.44.e20 |
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author | Kim, Sunil Lee, Sukjoon Jung, Han-Sung Kim, Sun-Young Kim, Euiseong |
author_facet | Kim, Sunil Lee, Sukjoon Jung, Han-Sung Kim, Sun-Young Kim, Euiseong |
author_sort | Kim, Sunil |
collection | PubMed |
description | OBJECTIVES: To achieve pulp-dentin complex regeneration with tissue engineering, treatment efficacies and safeties should be evaluated using in vivo orthotopic transplantation in a sufficient number of animals. Mice have been a species of choice in which to study stem cell biology in mammals. However, most pulp-dentin complex regeneration studies have used large animals because the mouse tooth is too small. The purpose of this study was to demonstrate the utility of the mouse tooth as a transplantation model for pulp-dentin complex regeneration research. MATERIALS AND METHODS: Experiments were performed using 7-week-old male Institute of Cancer Research (ICR) mice; a total of 35 mice had their pulp exposed, and 5 mice each were sacrificed at 1, 2, 4, 7, 9, 12 and 14 days after pulp exposure. After decalcification in 5% ethylenediaminetetraacetic acid, the samples were embedded and cut with a microtome and then stained with hematoxylin and eosin. Slides were observed under a high-magnification light microscope. RESULTS: Until 1 week postoperatively, the tissue below the pulp chamber orifice appeared normal. The remaining coronal portion of the pulp tissue was inflammatory and necrotic. After 1 week postoperatively, inflammation and necrosis were apparent in the root canals inferior to the orifices. The specimens obtained after experimental day 14 showed necrosis of all tissue in the root canals. CONCLUSIONS: This study could provide opportunities for researchers performing in vivo orthotopic transplantation experiments with mice. |
format | Online Article Text |
id | pubmed-6529795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Academy of Conservative Dentistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-65297952019-05-30 Development of a mouse model for pulp-dentin complex regeneration research: a preliminary study Kim, Sunil Lee, Sukjoon Jung, Han-Sung Kim, Sun-Young Kim, Euiseong Restor Dent Endod Research Article OBJECTIVES: To achieve pulp-dentin complex regeneration with tissue engineering, treatment efficacies and safeties should be evaluated using in vivo orthotopic transplantation in a sufficient number of animals. Mice have been a species of choice in which to study stem cell biology in mammals. However, most pulp-dentin complex regeneration studies have used large animals because the mouse tooth is too small. The purpose of this study was to demonstrate the utility of the mouse tooth as a transplantation model for pulp-dentin complex regeneration research. MATERIALS AND METHODS: Experiments were performed using 7-week-old male Institute of Cancer Research (ICR) mice; a total of 35 mice had their pulp exposed, and 5 mice each were sacrificed at 1, 2, 4, 7, 9, 12 and 14 days after pulp exposure. After decalcification in 5% ethylenediaminetetraacetic acid, the samples were embedded and cut with a microtome and then stained with hematoxylin and eosin. Slides were observed under a high-magnification light microscope. RESULTS: Until 1 week postoperatively, the tissue below the pulp chamber orifice appeared normal. The remaining coronal portion of the pulp tissue was inflammatory and necrotic. After 1 week postoperatively, inflammation and necrosis were apparent in the root canals inferior to the orifices. The specimens obtained after experimental day 14 showed necrosis of all tissue in the root canals. CONCLUSIONS: This study could provide opportunities for researchers performing in vivo orthotopic transplantation experiments with mice. The Korean Academy of Conservative Dentistry 2019-05-07 /pmc/articles/PMC6529795/ /pubmed/31149618 http://dx.doi.org/10.5395/rde.2019.44.e20 Text en Copyright © 2019. The Korean Academy of Conservative Dentistry https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kim, Sunil Lee, Sukjoon Jung, Han-Sung Kim, Sun-Young Kim, Euiseong Development of a mouse model for pulp-dentin complex regeneration research: a preliminary study |
title | Development of a mouse model for pulp-dentin complex regeneration research: a preliminary study |
title_full | Development of a mouse model for pulp-dentin complex regeneration research: a preliminary study |
title_fullStr | Development of a mouse model for pulp-dentin complex regeneration research: a preliminary study |
title_full_unstemmed | Development of a mouse model for pulp-dentin complex regeneration research: a preliminary study |
title_short | Development of a mouse model for pulp-dentin complex regeneration research: a preliminary study |
title_sort | development of a mouse model for pulp-dentin complex regeneration research: a preliminary study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529795/ https://www.ncbi.nlm.nih.gov/pubmed/31149618 http://dx.doi.org/10.5395/rde.2019.44.e20 |
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