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Multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns
Impaired wound healing is an immense medical challenge, and while autologous skin grafting remains the “gold-standard” therapeutic option for repairing wounds that cannot be closed by primary or secondary intention, it is limited by substantial donor site morbidity. We previously developed the alter...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814113/ https://www.ncbi.nlm.nih.gov/pubmed/33462350 http://dx.doi.org/10.1038/s41598-021-81179-7 |
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author | Fuchs, Christiane Pham, Linh Henderson, Jermaine Stalnaker, Katherine J. Anderson, R. Rox Tam, Joshua |
author_facet | Fuchs, Christiane Pham, Linh Henderson, Jermaine Stalnaker, Katherine J. Anderson, R. Rox Tam, Joshua |
author_sort | Fuchs, Christiane |
collection | PubMed |
description | Impaired wound healing is an immense medical challenge, and while autologous skin grafting remains the “gold-standard” therapeutic option for repairing wounds that cannot be closed by primary or secondary intention, it is limited by substantial donor site morbidity. We previously developed the alternative approach of harvesting full-thickness skin tissue in the form of “micro skin tissue columns” (MSTCs), without causing scarring or any other long-term morbidity. In this study we investigated how MSTC treatment affects the different cellular processes involved in wound healing. We found that MSTC-derived cells were able to remodel and repopulate the wound volume, and positively impact multiple aspects of the wound healing process, including accelerating re-epithelialization by providing multiple cell sources throughout the wound area, increasing collagen deposition, enhancing dermal remodeling, and attenuating the inflammatory response. These effects combined to enhance both epidermal and dermal wound healing. This MSTC treatment approach was designed for practical clinical use, could convey many benefits of autologous skin grafting, and avoids the major drawback of donor site morbidity. |
format | Online Article Text |
id | pubmed-7814113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78141132021-01-21 Multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns Fuchs, Christiane Pham, Linh Henderson, Jermaine Stalnaker, Katherine J. Anderson, R. Rox Tam, Joshua Sci Rep Article Impaired wound healing is an immense medical challenge, and while autologous skin grafting remains the “gold-standard” therapeutic option for repairing wounds that cannot be closed by primary or secondary intention, it is limited by substantial donor site morbidity. We previously developed the alternative approach of harvesting full-thickness skin tissue in the form of “micro skin tissue columns” (MSTCs), without causing scarring or any other long-term morbidity. In this study we investigated how MSTC treatment affects the different cellular processes involved in wound healing. We found that MSTC-derived cells were able to remodel and repopulate the wound volume, and positively impact multiple aspects of the wound healing process, including accelerating re-epithelialization by providing multiple cell sources throughout the wound area, increasing collagen deposition, enhancing dermal remodeling, and attenuating the inflammatory response. These effects combined to enhance both epidermal and dermal wound healing. This MSTC treatment approach was designed for practical clinical use, could convey many benefits of autologous skin grafting, and avoids the major drawback of donor site morbidity. Nature Publishing Group UK 2021-01-18 /pmc/articles/PMC7814113/ /pubmed/33462350 http://dx.doi.org/10.1038/s41598-021-81179-7 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fuchs, Christiane Pham, Linh Henderson, Jermaine Stalnaker, Katherine J. Anderson, R. Rox Tam, Joshua Multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns |
title | Multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns |
title_full | Multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns |
title_fullStr | Multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns |
title_full_unstemmed | Multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns |
title_short | Multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns |
title_sort | multi-faceted enhancement of full-thickness skin wound healing by treatment with autologous micro skin tissue columns |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814113/ https://www.ncbi.nlm.nih.gov/pubmed/33462350 http://dx.doi.org/10.1038/s41598-021-81179-7 |
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