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Investigation of biomaterials by human epithelial gingiva cells: an in vitro study
INTRODUCTION: In modern medicine and dentistry the use of biomaterials is a fast developing field of increasing interest. Especially in dentistry the interaction between biomaterials like implant materials and the soft tissue in the oral cavity is in the focus of daily research. In this context the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549823/ https://www.ncbi.nlm.nih.gov/pubmed/23241143 http://dx.doi.org/10.1186/1746-160X-8-35 |
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author | Neunzehn, Jörg Lüttenberg, Beate Wiesmann, Hans-Peter |
author_facet | Neunzehn, Jörg Lüttenberg, Beate Wiesmann, Hans-Peter |
author_sort | Neunzehn, Jörg |
collection | PubMed |
description | INTRODUCTION: In modern medicine and dentistry the use of biomaterials is a fast developing field of increasing interest. Especially in dentistry the interaction between biomaterials like implant materials and the soft tissue in the oral cavity is in the focus of daily research. In this context the high importance of testing materials and their surfaces concerning their biocompatibility towards corresponding cells is very likely. For this purpose this study investigates cells derived from human gingival biopsies on different materials and surfaces. METHODS: Cells in this study were cultivated out of human biopsies by a grow out explant technique and were sub cultivated on titanium, zirconium dioxide and collagen membrane specimens. To characterise the cells on the material surfaces used in this study immunohistochemical and histological staining techniques as well as different methods of microscopy (light microscopy and SEM) were applied. RESULTS: With the aid of the explant technique and the chosen cell cultivation method it was possible to investigate the human gingiva derived cells on different materials. The data of the present study show that the human gingival cells attach and proliferate on all three tested materials by exhibiting characteristic gingival keratinocyte protein expression even after long periods of culture e.g. up to 70 days. CONCLUSIONS: It could be shown that the three tested materials titanium, zirconium dioxide and collagen membrane (and their special surfaces) are good candidates for the application as materials in the dental gingival environment or, in the case of the collagen membrane as scaffold/cell-carrier for human gingival cells in tissue engineering. |
format | Online Article Text |
id | pubmed-3549823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35498232013-01-23 Investigation of biomaterials by human epithelial gingiva cells: an in vitro study Neunzehn, Jörg Lüttenberg, Beate Wiesmann, Hans-Peter Head Face Med Research INTRODUCTION: In modern medicine and dentistry the use of biomaterials is a fast developing field of increasing interest. Especially in dentistry the interaction between biomaterials like implant materials and the soft tissue in the oral cavity is in the focus of daily research. In this context the high importance of testing materials and their surfaces concerning their biocompatibility towards corresponding cells is very likely. For this purpose this study investigates cells derived from human gingival biopsies on different materials and surfaces. METHODS: Cells in this study were cultivated out of human biopsies by a grow out explant technique and were sub cultivated on titanium, zirconium dioxide and collagen membrane specimens. To characterise the cells on the material surfaces used in this study immunohistochemical and histological staining techniques as well as different methods of microscopy (light microscopy and SEM) were applied. RESULTS: With the aid of the explant technique and the chosen cell cultivation method it was possible to investigate the human gingiva derived cells on different materials. The data of the present study show that the human gingival cells attach and proliferate on all three tested materials by exhibiting characteristic gingival keratinocyte protein expression even after long periods of culture e.g. up to 70 days. CONCLUSIONS: It could be shown that the three tested materials titanium, zirconium dioxide and collagen membrane (and their special surfaces) are good candidates for the application as materials in the dental gingival environment or, in the case of the collagen membrane as scaffold/cell-carrier for human gingival cells in tissue engineering. BioMed Central 2012-12-15 /pmc/articles/PMC3549823/ /pubmed/23241143 http://dx.doi.org/10.1186/1746-160X-8-35 Text en Copyright ©2012 Neunzehn et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Neunzehn, Jörg Lüttenberg, Beate Wiesmann, Hans-Peter Investigation of biomaterials by human epithelial gingiva cells: an in vitro study |
title | Investigation of biomaterials by human epithelial gingiva cells: an in vitro study |
title_full | Investigation of biomaterials by human epithelial gingiva cells: an in vitro study |
title_fullStr | Investigation of biomaterials by human epithelial gingiva cells: an in vitro study |
title_full_unstemmed | Investigation of biomaterials by human epithelial gingiva cells: an in vitro study |
title_short | Investigation of biomaterials by human epithelial gingiva cells: an in vitro study |
title_sort | investigation of biomaterials by human epithelial gingiva cells: an in vitro study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549823/ https://www.ncbi.nlm.nih.gov/pubmed/23241143 http://dx.doi.org/10.1186/1746-160X-8-35 |
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