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Effect of a DACC-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model
Wound dressings that exert an antimicrobial effect in order to prevent and treat wound infections can be harmful to the wound healing process. Dressings with hydrophobic coatings, however, have been suggested to both reduce the microbial load and promote the healing process. Therefore, the potential...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825393/ https://www.ncbi.nlm.nih.gov/pubmed/35133505 http://dx.doi.org/10.1007/s10856-022-06648-5 |
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author | Morgner, Bianka Husmark, Johanna Arvidsson, Anna Wiegand, Cornelia |
author_facet | Morgner, Bianka Husmark, Johanna Arvidsson, Anna Wiegand, Cornelia |
author_sort | Morgner, Bianka |
collection | PubMed |
description | Wound dressings that exert an antimicrobial effect in order to prevent and treat wound infections can be harmful to the wound healing process. Dressings with hydrophobic coatings, however, have been suggested to both reduce the microbial load and promote the healing process. Therefore, the potential effects of a dialkylcarbamoyl chloride (DACC)-coated dressing on fibroblasts and keratinocytes in wound healing were studied using mechanical scratch wounding of confluent cell layers as an in vitro model. Additionally, gene expression analysis by qRT-PCR was used to elucidate the longitudinal effects of the DACC-coated dressing on cell responses, specifically inflammation, growth factor induction and collagen synthesis. DACC promoted cell viability, did not stick to the cell layers, and supported normal wound healing progression in vitro. In contrast, cells became attached to the uncoated reference material, which inhibited scratch closure. Moreover, DACC slightly induced KGF, VEGF, and GM-CSF expression in HaCaT cells and NHDF. Physiological COL1A1 and COL3A1 gene expression by NHDF was observed under DACC treatment with no observable effect on S100A7 and RNASE7 levels in HaCaT cells. Overall, the DACC coating was found to be safe and may positively influence the wound healing outcome. [Figure: see text] |
format | Online Article Text |
id | pubmed-8825393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-88253932022-02-23 Effect of a DACC-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model Morgner, Bianka Husmark, Johanna Arvidsson, Anna Wiegand, Cornelia J Mater Sci Mater Med Biocompatibility Studies Wound dressings that exert an antimicrobial effect in order to prevent and treat wound infections can be harmful to the wound healing process. Dressings with hydrophobic coatings, however, have been suggested to both reduce the microbial load and promote the healing process. Therefore, the potential effects of a dialkylcarbamoyl chloride (DACC)-coated dressing on fibroblasts and keratinocytes in wound healing were studied using mechanical scratch wounding of confluent cell layers as an in vitro model. Additionally, gene expression analysis by qRT-PCR was used to elucidate the longitudinal effects of the DACC-coated dressing on cell responses, specifically inflammation, growth factor induction and collagen synthesis. DACC promoted cell viability, did not stick to the cell layers, and supported normal wound healing progression in vitro. In contrast, cells became attached to the uncoated reference material, which inhibited scratch closure. Moreover, DACC slightly induced KGF, VEGF, and GM-CSF expression in HaCaT cells and NHDF. Physiological COL1A1 and COL3A1 gene expression by NHDF was observed under DACC treatment with no observable effect on S100A7 and RNASE7 levels in HaCaT cells. Overall, the DACC coating was found to be safe and may positively influence the wound healing outcome. [Figure: see text] Springer US 2022-02-08 2022 /pmc/articles/PMC8825393/ /pubmed/35133505 http://dx.doi.org/10.1007/s10856-022-06648-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biocompatibility Studies Morgner, Bianka Husmark, Johanna Arvidsson, Anna Wiegand, Cornelia Effect of a DACC-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model |
title | Effect of a DACC-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model |
title_full | Effect of a DACC-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model |
title_fullStr | Effect of a DACC-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model |
title_full_unstemmed | Effect of a DACC-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model |
title_short | Effect of a DACC-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model |
title_sort | effect of a dacc-coated dressing on keratinocytes and fibroblasts in wound healing using an in vitro scratch model |
topic | Biocompatibility Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825393/ https://www.ncbi.nlm.nih.gov/pubmed/35133505 http://dx.doi.org/10.1007/s10856-022-06648-5 |
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