Osteogenic Cell Behavior on Titanium Surfaces in Hard Tissue
It is challenging to remove dental implants once they have been inserted into the bone because it is hard to visualize the actual process of bone formation after implant installation, not to mention the cellular events that occur therein. During bone formation, contact osteogenesis occurs on roughen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571803/ https://www.ncbi.nlm.nih.gov/pubmed/31052572 http://dx.doi.org/10.3390/jcm8050604 |
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author | Choi, Jung-Yoo Albrektsson, Tomas Jeon, Young-Jun Yeo, In-Sung Luke |
author_facet | Choi, Jung-Yoo Albrektsson, Tomas Jeon, Young-Jun Yeo, In-Sung Luke |
author_sort | Choi, Jung-Yoo |
collection | PubMed |
description | It is challenging to remove dental implants once they have been inserted into the bone because it is hard to visualize the actual process of bone formation after implant installation, not to mention the cellular events that occur therein. During bone formation, contact osteogenesis occurs on roughened implant surfaces, while distance osteogenesis occurs on smooth implant surfaces. In the literature, there have been many in vitro model studies of bone formation on simulated dental implants using flattened titanium (Ti) discs; however, the purpose of this study was to identify the in vivo cell responses to the implant surfaces on actual, three-dimensional (3D) dental Ti implants and the surrounding bone in contact with such implants at the electron microscopic level using two different types of implant surfaces. In particular, the different parts of the implant structures were scrutinized. In this study, dental implants were installed in rabbit tibiae. The implants and bone were removed on day 10 and, subsequently, assessed using scanning electron microscopy (SEM), immunofluorescence microscopy (IF), transmission electron microscopy (TEM), focused ion-beam (FIB) system with Cs-corrected TEM (Cs-STEM), and confocal laser scanning microscopy (CLSM)—which were used to determine the implant surface characteristics and to identify the cells according to the different structural parts of the turned and roughened implants. The cell attachment pattern was revealed according to the different structural components of each implant surface and bone. Different cell responses to the implant surfaces and the surrounding bone were attained at an electron microscopic level in an in vivo model. These results shed light on cell behavioral patterns that occur during bone regeneration and could be a guide in the use of electron microscopy for 3D dental implants in an in vivo model. |
format | Online Article Text |
id | pubmed-6571803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65718032019-06-18 Osteogenic Cell Behavior on Titanium Surfaces in Hard Tissue Choi, Jung-Yoo Albrektsson, Tomas Jeon, Young-Jun Yeo, In-Sung Luke J Clin Med Article It is challenging to remove dental implants once they have been inserted into the bone because it is hard to visualize the actual process of bone formation after implant installation, not to mention the cellular events that occur therein. During bone formation, contact osteogenesis occurs on roughened implant surfaces, while distance osteogenesis occurs on smooth implant surfaces. In the literature, there have been many in vitro model studies of bone formation on simulated dental implants using flattened titanium (Ti) discs; however, the purpose of this study was to identify the in vivo cell responses to the implant surfaces on actual, three-dimensional (3D) dental Ti implants and the surrounding bone in contact with such implants at the electron microscopic level using two different types of implant surfaces. In particular, the different parts of the implant structures were scrutinized. In this study, dental implants were installed in rabbit tibiae. The implants and bone were removed on day 10 and, subsequently, assessed using scanning electron microscopy (SEM), immunofluorescence microscopy (IF), transmission electron microscopy (TEM), focused ion-beam (FIB) system with Cs-corrected TEM (Cs-STEM), and confocal laser scanning microscopy (CLSM)—which were used to determine the implant surface characteristics and to identify the cells according to the different structural parts of the turned and roughened implants. The cell attachment pattern was revealed according to the different structural components of each implant surface and bone. Different cell responses to the implant surfaces and the surrounding bone were attained at an electron microscopic level in an in vivo model. These results shed light on cell behavioral patterns that occur during bone regeneration and could be a guide in the use of electron microscopy for 3D dental implants in an in vivo model. MDPI 2019-05-02 /pmc/articles/PMC6571803/ /pubmed/31052572 http://dx.doi.org/10.3390/jcm8050604 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Choi, Jung-Yoo Albrektsson, Tomas Jeon, Young-Jun Yeo, In-Sung Luke Osteogenic Cell Behavior on Titanium Surfaces in Hard Tissue |
title | Osteogenic Cell Behavior on Titanium Surfaces in Hard Tissue |
title_full | Osteogenic Cell Behavior on Titanium Surfaces in Hard Tissue |
title_fullStr | Osteogenic Cell Behavior on Titanium Surfaces in Hard Tissue |
title_full_unstemmed | Osteogenic Cell Behavior on Titanium Surfaces in Hard Tissue |
title_short | Osteogenic Cell Behavior on Titanium Surfaces in Hard Tissue |
title_sort | osteogenic cell behavior on titanium surfaces in hard tissue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571803/ https://www.ncbi.nlm.nih.gov/pubmed/31052572 http://dx.doi.org/10.3390/jcm8050604 |
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