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3D cellular visualization of intact mouse tooth using optical clearing without decalcification

Dental pulp is composed of nerves, blood vessels, and various types of cells and surrounded by a thick and hard enamel-dentin matrix. Due to its importance in the maintenance of tooth vitality, there have been intensive efforts to analyze the complex cellular-level organization of the dental pulp in...

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Autores principales: Hong, Sujung, Lee, Jingu, Kim, Jin Man, Kim, Sun-Young, Kim, Hyung-Ryong, Kim, Pilhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802633/
https://www.ncbi.nlm.nih.gov/pubmed/31451694
http://dx.doi.org/10.1038/s41368-019-0056-z
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author Hong, Sujung
Lee, Jingu
Kim, Jin Man
Kim, Sun-Young
Kim, Hyung-Ryong
Kim, Pilhan
author_facet Hong, Sujung
Lee, Jingu
Kim, Jin Man
Kim, Sun-Young
Kim, Hyung-Ryong
Kim, Pilhan
author_sort Hong, Sujung
collection PubMed
description Dental pulp is composed of nerves, blood vessels, and various types of cells and surrounded by a thick and hard enamel-dentin matrix. Due to its importance in the maintenance of tooth vitality, there have been intensive efforts to analyze the complex cellular-level organization of the dental pulp in teeth. Although conventional histologic analysis has provided microscopic images of the dental pulp, 3-dimensional (3D) cellular-level visualization of the whole dental pulp in an intact tooth has remained a technically challenging task. This is mainly due to the inevitable disruption and loss of microscopic structural features during the process of mechanical sectioning required for the preparation of the tooth sample for histological observation. To accomplish 3D microscopic observation of thick intact tissue, various optical clearing techniques have been developed mostly for soft tissue, and their application for hard tissues such as bone and teeth has only recently started to be investigated. In this work, we established a simple and rapid optical clearing technique for intact mouse teeth without the time-consuming process of decalcification. We achieved 3D cellular-level visualization of the microvasculature and various immune cell distributions in the whole dental pulp of mouse teeth under normal and pathologic conditions. This technique could be used to enable diverse research methods on tooth development and regeneration by providing 3D visualization of various pulpal cells in intact mouse teeth.
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spelling pubmed-68026332019-10-22 3D cellular visualization of intact mouse tooth using optical clearing without decalcification Hong, Sujung Lee, Jingu Kim, Jin Man Kim, Sun-Young Kim, Hyung-Ryong Kim, Pilhan Int J Oral Sci Article Dental pulp is composed of nerves, blood vessels, and various types of cells and surrounded by a thick and hard enamel-dentin matrix. Due to its importance in the maintenance of tooth vitality, there have been intensive efforts to analyze the complex cellular-level organization of the dental pulp in teeth. Although conventional histologic analysis has provided microscopic images of the dental pulp, 3-dimensional (3D) cellular-level visualization of the whole dental pulp in an intact tooth has remained a technically challenging task. This is mainly due to the inevitable disruption and loss of microscopic structural features during the process of mechanical sectioning required for the preparation of the tooth sample for histological observation. To accomplish 3D microscopic observation of thick intact tissue, various optical clearing techniques have been developed mostly for soft tissue, and their application for hard tissues such as bone and teeth has only recently started to be investigated. In this work, we established a simple and rapid optical clearing technique for intact mouse teeth without the time-consuming process of decalcification. We achieved 3D cellular-level visualization of the microvasculature and various immune cell distributions in the whole dental pulp of mouse teeth under normal and pathologic conditions. This technique could be used to enable diverse research methods on tooth development and regeneration by providing 3D visualization of various pulpal cells in intact mouse teeth. Nature Publishing Group UK 2019-08-27 /pmc/articles/PMC6802633/ /pubmed/31451694 http://dx.doi.org/10.1038/s41368-019-0056-z Text en © The Author(s) 2019 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
Hong, Sujung
Lee, Jingu
Kim, Jin Man
Kim, Sun-Young
Kim, Hyung-Ryong
Kim, Pilhan
3D cellular visualization of intact mouse tooth using optical clearing without decalcification
title 3D cellular visualization of intact mouse tooth using optical clearing without decalcification
title_full 3D cellular visualization of intact mouse tooth using optical clearing without decalcification
title_fullStr 3D cellular visualization of intact mouse tooth using optical clearing without decalcification
title_full_unstemmed 3D cellular visualization of intact mouse tooth using optical clearing without decalcification
title_short 3D cellular visualization of intact mouse tooth using optical clearing without decalcification
title_sort 3d cellular visualization of intact mouse tooth using optical clearing without decalcification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802633/
https://www.ncbi.nlm.nih.gov/pubmed/31451694
http://dx.doi.org/10.1038/s41368-019-0056-z
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