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Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts
Enamel matrix derivative is used to promote periodontal regeneration during the corrective phase of the treatment of periodontal defects. Our main goal was to analyze the bioactivity of different molecular weight fractions of enamel matrix derivative. Enamel matrix derivative, a complex mixture of p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456328/ https://www.ncbi.nlm.nih.gov/pubmed/26090085 http://dx.doi.org/10.1177/2041731415575857 |
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author | Villa, Oscar Brookes, Steven J Thiede, Bernd Heijl, Lars Lyngstadaas, Staale P Reseland, Janne E |
author_facet | Villa, Oscar Brookes, Steven J Thiede, Bernd Heijl, Lars Lyngstadaas, Staale P Reseland, Janne E |
author_sort | Villa, Oscar |
collection | PubMed |
description | Enamel matrix derivative is used to promote periodontal regeneration during the corrective phase of the treatment of periodontal defects. Our main goal was to analyze the bioactivity of different molecular weight fractions of enamel matrix derivative. Enamel matrix derivative, a complex mixture of proteins, was separated into 13 fractions using size-exclusion chromatography and characterized by sodium dodecyl sulfate–polyacrylamide gel electrophoresis and liquid chromatography–electrospray ionization–tandem mass spectrometry. Human periodontal ligament fibroblasts were treated with either enamel matrix derivative or the different fractions. Proliferation and cytokine secretion to the cell culture medium were measured and compared to untreated cells. The liquid chromatography–electrospray ionization–tandem mass spectrometry analyses revealed that the most abundant peptides were amelogenin and leucine-rich amelogenin peptide related. The fractions containing proteins above 20 kDa induced an increase in vascular endothelial growth factor and interleukin-6 secretion, whereas lower molecular weight fractions enhanced proliferation and secretion of interleukin-8 and monocyte chemoattractant protein-1 and reduced interleukin-4 release. The various molecular components in the enamel matrix derivative formulation might contribute to reported effects on tissue regeneration through their influence on vascularization, the immune response, and chemotaxis. |
format | Online Article Text |
id | pubmed-4456328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-44563282015-06-18 Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts Villa, Oscar Brookes, Steven J Thiede, Bernd Heijl, Lars Lyngstadaas, Staale P Reseland, Janne E J Tissue Eng Original Article Enamel matrix derivative is used to promote periodontal regeneration during the corrective phase of the treatment of periodontal defects. Our main goal was to analyze the bioactivity of different molecular weight fractions of enamel matrix derivative. Enamel matrix derivative, a complex mixture of proteins, was separated into 13 fractions using size-exclusion chromatography and characterized by sodium dodecyl sulfate–polyacrylamide gel electrophoresis and liquid chromatography–electrospray ionization–tandem mass spectrometry. Human periodontal ligament fibroblasts were treated with either enamel matrix derivative or the different fractions. Proliferation and cytokine secretion to the cell culture medium were measured and compared to untreated cells. The liquid chromatography–electrospray ionization–tandem mass spectrometry analyses revealed that the most abundant peptides were amelogenin and leucine-rich amelogenin peptide related. The fractions containing proteins above 20 kDa induced an increase in vascular endothelial growth factor and interleukin-6 secretion, whereas lower molecular weight fractions enhanced proliferation and secretion of interleukin-8 and monocyte chemoattractant protein-1 and reduced interleukin-4 release. The various molecular components in the enamel matrix derivative formulation might contribute to reported effects on tissue regeneration through their influence on vascularization, the immune response, and chemotaxis. SAGE Publications 2015-03-19 /pmc/articles/PMC4456328/ /pubmed/26090085 http://dx.doi.org/10.1177/2041731415575857 Text en © The Author(s) 2015 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 Villa, Oscar Brookes, Steven J Thiede, Bernd Heijl, Lars Lyngstadaas, Staale P Reseland, Janne E Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts |
title | Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts |
title_full | Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts |
title_fullStr | Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts |
title_full_unstemmed | Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts |
title_short | Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts |
title_sort | subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456328/ https://www.ncbi.nlm.nih.gov/pubmed/26090085 http://dx.doi.org/10.1177/2041731415575857 |
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