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Cell Population Kinetics of Collagen Scaffolds in Ex Vivo Oral Wound Repair

Biodegradable collagen scaffolds are used clinically for oral soft tissue augmentation to support wound healing. This study sought to provide a novel ex vivo model for analyzing healing kinetics and gene expression of primary human gingival fibroblasts (hGF) within collagen scaffolds. Sponge type an...

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Autores principales: Agis, Hermann, Collins, Amy, Taut, Andrei D., Jin, Qiming, Kruger, Laura, Görlach, Christoph, Giannobile, William V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232419/
https://www.ncbi.nlm.nih.gov/pubmed/25397671
http://dx.doi.org/10.1371/journal.pone.0112680
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author Agis, Hermann
Collins, Amy
Taut, Andrei D.
Jin, Qiming
Kruger, Laura
Görlach, Christoph
Giannobile, William V.
author_facet Agis, Hermann
Collins, Amy
Taut, Andrei D.
Jin, Qiming
Kruger, Laura
Görlach, Christoph
Giannobile, William V.
author_sort Agis, Hermann
collection PubMed
description Biodegradable collagen scaffolds are used clinically for oral soft tissue augmentation to support wound healing. This study sought to provide a novel ex vivo model for analyzing healing kinetics and gene expression of primary human gingival fibroblasts (hGF) within collagen scaffolds. Sponge type and gel type scaffolds with and without platelet-derived growth factor-BB (PDGF) were assessed in an hGF containing matrix. Morphology was evaluated with scanning electron microscopy, and hGF metabolic activity using MTT. We quantitated the population kinetics within the scaffolds based on cell density and distance from the scaffold border of DiI-labled hGFs over a two-week observation period. Gene expression was evaluated with gene array and qPCR. The sponge type scaffolds showed a porous morphology. Absolute cell number and distance was higher in sponge type scaffolds when compared to gel type scaffolds, in particular during the first week of observation. PDGF incorporated scaffolds increased cell numbers, distance, and formazan formation in the MTT assay. Gene expression dynamics revealed the induction of key genes associated with the generation of oral tissue. DKK1, CYR61, CTGF, TGFBR1 levels were increased and integrin ITGA2 levels were decreased in the sponge type scaffolds compared to the gel type scaffold. The results suggest that this novel model of oral wound healing provides insights into population kinetics and gene expression dynamics of biodegradable scaffolds.
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spelling pubmed-42324192014-11-26 Cell Population Kinetics of Collagen Scaffolds in Ex Vivo Oral Wound Repair Agis, Hermann Collins, Amy Taut, Andrei D. Jin, Qiming Kruger, Laura Görlach, Christoph Giannobile, William V. PLoS One Research Article Biodegradable collagen scaffolds are used clinically for oral soft tissue augmentation to support wound healing. This study sought to provide a novel ex vivo model for analyzing healing kinetics and gene expression of primary human gingival fibroblasts (hGF) within collagen scaffolds. Sponge type and gel type scaffolds with and without platelet-derived growth factor-BB (PDGF) were assessed in an hGF containing matrix. Morphology was evaluated with scanning electron microscopy, and hGF metabolic activity using MTT. We quantitated the population kinetics within the scaffolds based on cell density and distance from the scaffold border of DiI-labled hGFs over a two-week observation period. Gene expression was evaluated with gene array and qPCR. The sponge type scaffolds showed a porous morphology. Absolute cell number and distance was higher in sponge type scaffolds when compared to gel type scaffolds, in particular during the first week of observation. PDGF incorporated scaffolds increased cell numbers, distance, and formazan formation in the MTT assay. Gene expression dynamics revealed the induction of key genes associated with the generation of oral tissue. DKK1, CYR61, CTGF, TGFBR1 levels were increased and integrin ITGA2 levels were decreased in the sponge type scaffolds compared to the gel type scaffold. The results suggest that this novel model of oral wound healing provides insights into population kinetics and gene expression dynamics of biodegradable scaffolds. Public Library of Science 2014-11-14 /pmc/articles/PMC4232419/ /pubmed/25397671 http://dx.doi.org/10.1371/journal.pone.0112680 Text en © 2014 Agis et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Agis, Hermann
Collins, Amy
Taut, Andrei D.
Jin, Qiming
Kruger, Laura
Görlach, Christoph
Giannobile, William V.
Cell Population Kinetics of Collagen Scaffolds in Ex Vivo Oral Wound Repair
title Cell Population Kinetics of Collagen Scaffolds in Ex Vivo Oral Wound Repair
title_full Cell Population Kinetics of Collagen Scaffolds in Ex Vivo Oral Wound Repair
title_fullStr Cell Population Kinetics of Collagen Scaffolds in Ex Vivo Oral Wound Repair
title_full_unstemmed Cell Population Kinetics of Collagen Scaffolds in Ex Vivo Oral Wound Repair
title_short Cell Population Kinetics of Collagen Scaffolds in Ex Vivo Oral Wound Repair
title_sort cell population kinetics of collagen scaffolds in ex vivo oral wound repair
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232419/
https://www.ncbi.nlm.nih.gov/pubmed/25397671
http://dx.doi.org/10.1371/journal.pone.0112680
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