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Bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo
Royal jelly (RJ) has successfully been used as a remedy in wound healing. RJ has multiple effects, including antibacterial, anti-inflammatory and immunomodulatory activities, in various cell types. However, no component(s) (other than antibacterial) have been identified in RJ-accelerated wound heali...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544694/ https://www.ncbi.nlm.nih.gov/pubmed/28779102 http://dx.doi.org/10.1038/s41598-017-07494-0 |
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author | Bucekova, Marcela Sojka, Martin Valachova, Ivana Martinotti, Simona Ranzato, Elia Szep, Zoltan Majtan, Viktor Klaudiny, Jaroslav Majtan, Juraj |
author_facet | Bucekova, Marcela Sojka, Martin Valachova, Ivana Martinotti, Simona Ranzato, Elia Szep, Zoltan Majtan, Viktor Klaudiny, Jaroslav Majtan, Juraj |
author_sort | Bucekova, Marcela |
collection | PubMed |
description | Royal jelly (RJ) has successfully been used as a remedy in wound healing. RJ has multiple effects, including antibacterial, anti-inflammatory and immunomodulatory activities, in various cell types. However, no component(s) (other than antibacterial) have been identified in RJ-accelerated wound healing. In this study, we demonstrate that keratinocytes are responsible for the elevated production of matrix metalloproteinase-9 (MMP-9) after incubation with a water extract of RJ. Furthermore, the keratinocyte migration and wound closure rates were significantly increased in the presence of RJ extract. MMP-9 production was reduced significantly following proteinase K treatment but remained stable after heat treatment, indicating that active component(s) have a proteinous character. To identify the component responsible for inducing MMP-9 production, RJ extract was fractionated using C18 RP-HPLC. In fractions exhibiting stimulatory activity, we immunochemically detected the bee-derived antibacterial peptide, defensin-1. Defensin-1 was cloned, and recombinant peptide was produced in a baculoviral expression system. Defensin-1 stimulated MMP-9 secretion from keratinocytes and increased keratinocyte migration and wound closure in vitro. In addition, defensin-1 promoted re-epithelisation and wound closure in uninfected excision wounds. These data indisputably demonstrate that defensin-1, a regular but concentration variable factor found in honey and RJ, contributes to cutaneous wound closure by enhancing keratinocyte migration and MMP-9 secretion. |
format | Online Article Text |
id | pubmed-5544694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55446942017-08-07 Bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo Bucekova, Marcela Sojka, Martin Valachova, Ivana Martinotti, Simona Ranzato, Elia Szep, Zoltan Majtan, Viktor Klaudiny, Jaroslav Majtan, Juraj Sci Rep Article Royal jelly (RJ) has successfully been used as a remedy in wound healing. RJ has multiple effects, including antibacterial, anti-inflammatory and immunomodulatory activities, in various cell types. However, no component(s) (other than antibacterial) have been identified in RJ-accelerated wound healing. In this study, we demonstrate that keratinocytes are responsible for the elevated production of matrix metalloproteinase-9 (MMP-9) after incubation with a water extract of RJ. Furthermore, the keratinocyte migration and wound closure rates were significantly increased in the presence of RJ extract. MMP-9 production was reduced significantly following proteinase K treatment but remained stable after heat treatment, indicating that active component(s) have a proteinous character. To identify the component responsible for inducing MMP-9 production, RJ extract was fractionated using C18 RP-HPLC. In fractions exhibiting stimulatory activity, we immunochemically detected the bee-derived antibacterial peptide, defensin-1. Defensin-1 was cloned, and recombinant peptide was produced in a baculoviral expression system. Defensin-1 stimulated MMP-9 secretion from keratinocytes and increased keratinocyte migration and wound closure in vitro. In addition, defensin-1 promoted re-epithelisation and wound closure in uninfected excision wounds. These data indisputably demonstrate that defensin-1, a regular but concentration variable factor found in honey and RJ, contributes to cutaneous wound closure by enhancing keratinocyte migration and MMP-9 secretion. Nature Publishing Group UK 2017-08-04 /pmc/articles/PMC5544694/ /pubmed/28779102 http://dx.doi.org/10.1038/s41598-017-07494-0 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Bucekova, Marcela Sojka, Martin Valachova, Ivana Martinotti, Simona Ranzato, Elia Szep, Zoltan Majtan, Viktor Klaudiny, Jaroslav Majtan, Juraj Bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo |
title | Bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo |
title_full | Bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo |
title_fullStr | Bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo |
title_full_unstemmed | Bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo |
title_short | Bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo |
title_sort | bee-derived antibacterial peptide, defensin-1, promotes wound re-epithelialisation in vitro and in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544694/ https://www.ncbi.nlm.nih.gov/pubmed/28779102 http://dx.doi.org/10.1038/s41598-017-07494-0 |
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