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Non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration
Adequate and rapid mucosal regeneration is one of the most important factors in the healing process of nasal mucosa after surgery or trauma. In particular, delayed mucosal regeneration after surgery is an important cause of surgical failure. However, no effective treatment is available yet. Non-ther...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137218/ https://www.ncbi.nlm.nih.gov/pubmed/30213992 http://dx.doi.org/10.1038/s41598-018-32077-y |
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author | Won, Ho-Ryun Kang, Sung Un Kim, Haeng Jun Jang, Jeon Yeob Shin, Yoo Seob Kim, Chul-Ho |
author_facet | Won, Ho-Ryun Kang, Sung Un Kim, Haeng Jun Jang, Jeon Yeob Shin, Yoo Seob Kim, Chul-Ho |
author_sort | Won, Ho-Ryun |
collection | PubMed |
description | Adequate and rapid mucosal regeneration is one of the most important factors in the healing process of nasal mucosa after surgery or trauma. In particular, delayed mucosal regeneration after surgery is an important cause of surgical failure. However, no effective treatment is available yet. Non-thermal plasma (NTP) has several medical effects, but the existing probe type is limited to local direct treatment. Therefore, we investigated the various effects using liquid type plasma to overcome this limitation. In addition, the therapeutic effects of non-thermal plasma treated solution (NTS) on nasal mucosa have yet to be determined. Experiments were carried out using BEAS-2B, a human bronchial epithelial cell line similar to nasal mucosa epithelium. NTS had no cytotoxicity to the BEAS-2B cells and enhanced cell proliferation. NTS also promoted migration of BEAS-2B cells. NTS increased cell proliferation and migration via epidermal growth factor receptor (EGFR) activities and epithelial-to-mesenchymal transition (EMT) signaling. Furthermore, NTS enhanced wound healing of nasal mucosa in an animal model. Accordingly, NTS promotes nasal mucosa wound healing by increasing cell proliferation and migration. These findings suggest the therapeutic potential of NTS in nasal mucosa wound healing. |
format | Online Article Text |
id | pubmed-6137218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61372182018-09-15 Non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration Won, Ho-Ryun Kang, Sung Un Kim, Haeng Jun Jang, Jeon Yeob Shin, Yoo Seob Kim, Chul-Ho Sci Rep Article Adequate and rapid mucosal regeneration is one of the most important factors in the healing process of nasal mucosa after surgery or trauma. In particular, delayed mucosal regeneration after surgery is an important cause of surgical failure. However, no effective treatment is available yet. Non-thermal plasma (NTP) has several medical effects, but the existing probe type is limited to local direct treatment. Therefore, we investigated the various effects using liquid type plasma to overcome this limitation. In addition, the therapeutic effects of non-thermal plasma treated solution (NTS) on nasal mucosa have yet to be determined. Experiments were carried out using BEAS-2B, a human bronchial epithelial cell line similar to nasal mucosa epithelium. NTS had no cytotoxicity to the BEAS-2B cells and enhanced cell proliferation. NTS also promoted migration of BEAS-2B cells. NTS increased cell proliferation and migration via epidermal growth factor receptor (EGFR) activities and epithelial-to-mesenchymal transition (EMT) signaling. Furthermore, NTS enhanced wound healing of nasal mucosa in an animal model. Accordingly, NTS promotes nasal mucosa wound healing by increasing cell proliferation and migration. These findings suggest the therapeutic potential of NTS in nasal mucosa wound healing. Nature Publishing Group UK 2018-09-13 /pmc/articles/PMC6137218/ /pubmed/30213992 http://dx.doi.org/10.1038/s41598-018-32077-y Text en © The Author(s) 2018 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 Won, Ho-Ryun Kang, Sung Un Kim, Haeng Jun Jang, Jeon Yeob Shin, Yoo Seob Kim, Chul-Ho Non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration |
title | Non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration |
title_full | Non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration |
title_fullStr | Non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration |
title_full_unstemmed | Non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration |
title_short | Non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration |
title_sort | non-thermal plasma treated solution with potential as a novel therapeutic agent for nasal mucosa regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137218/ https://www.ncbi.nlm.nih.gov/pubmed/30213992 http://dx.doi.org/10.1038/s41598-018-32077-y |
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