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The effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro

The purpose of this study was to compare, by means of in vitro cultivation technique, five marketed brands of wound covers used in the treatment of burns and other skin defects (Biobrane(®), Suprathel(®), Veloderm(®), Xe-Derma(®), and Xenoderm(®)) for their ability to stimulate the keratinocyte grow...

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Autores principales: Matoušková, Eva, Mestak, Ondrej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221924/
https://www.ncbi.nlm.nih.gov/pubmed/25383177
http://dx.doi.org/10.1177/2041731414554966
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author Matoušková, Eva
Mestak, Ondrej
author_facet Matoušková, Eva
Mestak, Ondrej
author_sort Matoušková, Eva
collection PubMed
description The purpose of this study was to compare, by means of in vitro cultivation technique, five marketed brands of wound covers used in the treatment of burns and other skin defects (Biobrane(®), Suprathel(®), Veloderm(®), Xe-Derma(®), and Xenoderm(®)) for their ability to stimulate the keratinocyte growth, stratification, and differentiation. In three independent experiments, human keratinocytes were grown on the tested covers in organotypic cultures by the 3T3 feeder layer technique. Vertical paraffin sections of the wound covers with keratinocytes were processed using hematoxylin–eosin staining and immunostaining for involucrin. Keratinocyte populations on the dressings were assessed for (1) number of keratinocyte strata (primary variable), (2) quantitative growth, (3) thickness of the keratinocyte layer, and (4) cell differentiation. The Xe-Derma wound cover provided the best support to keratinocyte proliferation and stratification, with the number of keratinocyte strata significantly (p < 0.05) higher in comparison to all products studied, except Xenoderm. However, in contrast to Xe-Derma, Xenoderm did not significantly differ from the other dressings. The results of this in vitro study show that the brands based on porcine dermal matrix possess the strongest effect on keratinocyte proliferation and stratification. The distinctive position of Xe-Derma may be related to its composition, where natural dermal fibers form a smooth surface, similar to the basement membrane. Furthermore, the results indicate that in vitro evaluation of effects on epithelial growth may accelerate the development of new bio-engineering-based wound covers.
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spelling pubmed-42219242014-11-07 The effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro Matoušková, Eva Mestak, Ondrej J Tissue Eng Original Article The purpose of this study was to compare, by means of in vitro cultivation technique, five marketed brands of wound covers used in the treatment of burns and other skin defects (Biobrane(®), Suprathel(®), Veloderm(®), Xe-Derma(®), and Xenoderm(®)) for their ability to stimulate the keratinocyte growth, stratification, and differentiation. In three independent experiments, human keratinocytes were grown on the tested covers in organotypic cultures by the 3T3 feeder layer technique. Vertical paraffin sections of the wound covers with keratinocytes were processed using hematoxylin–eosin staining and immunostaining for involucrin. Keratinocyte populations on the dressings were assessed for (1) number of keratinocyte strata (primary variable), (2) quantitative growth, (3) thickness of the keratinocyte layer, and (4) cell differentiation. The Xe-Derma wound cover provided the best support to keratinocyte proliferation and stratification, with the number of keratinocyte strata significantly (p < 0.05) higher in comparison to all products studied, except Xenoderm. However, in contrast to Xe-Derma, Xenoderm did not significantly differ from the other dressings. The results of this in vitro study show that the brands based on porcine dermal matrix possess the strongest effect on keratinocyte proliferation and stratification. The distinctive position of Xe-Derma may be related to its composition, where natural dermal fibers form a smooth surface, similar to the basement membrane. Furthermore, the results indicate that in vitro evaluation of effects on epithelial growth may accelerate the development of new bio-engineering-based wound covers. SAGE Publications 2014-10-14 /pmc/articles/PMC4221924/ /pubmed/25383177 http://dx.doi.org/10.1177/2041731414554966 Text en © The Author(s) 2014 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (http://www.uk.sagepub.com/aboutus/openaccess.htm).
spellingShingle Original Article
Matoušková, Eva
Mestak, Ondrej
The effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro
title The effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro
title_full The effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro
title_fullStr The effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro
title_full_unstemmed The effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro
title_short The effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro
title_sort effect of different biologic and biosynthetic wound covers on keratinocyte growth, stratification and differentiation in vitro
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221924/
https://www.ncbi.nlm.nih.gov/pubmed/25383177
http://dx.doi.org/10.1177/2041731414554966
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