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Reconstruction of functional human epidermis equivalent containing 5%IPS-derived keratinocytes treated with mitochondrial stimulating plant extracts
Reconstructed human epidermis equivalents (RHE) have been developed as a clinical skin substitute and as the replacement for animal testing in both research and industry. KiPS, or keratinocytes derived from induced pluripotent stem cells (iPSCs) are frequently used to generate RHE. In this study, we...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156774/ https://www.ncbi.nlm.nih.gov/pubmed/35641783 http://dx.doi.org/10.1038/s41598-022-13191-4 |
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author | Moreau, Marielle Capallere, Christophe Chavatte, Laurent Plaza, Christelle Meyrignac, Céline Pays, Karl Bavouzet, Bruno Botto, Jean-Marie Nizard, Carine Bulteau, Anne-Laure |
author_facet | Moreau, Marielle Capallere, Christophe Chavatte, Laurent Plaza, Christelle Meyrignac, Céline Pays, Karl Bavouzet, Bruno Botto, Jean-Marie Nizard, Carine Bulteau, Anne-Laure |
author_sort | Moreau, Marielle |
collection | PubMed |
description | Reconstructed human epidermis equivalents (RHE) have been developed as a clinical skin substitute and as the replacement for animal testing in both research and industry. KiPS, or keratinocytes derived from induced pluripotent stem cells (iPSCs) are frequently used to generate RHE. In this study, we focus on the mitochondrial performance of the KiPS derived from iPSCs obtained from two donors. We found that the KiPS derived from the older donor have more defective mitochondria. Treatment of these KiPS with a plant extract enriched in compounds known to protect mitochondria improved mitochondrial respiration and rendered them fully competent to derive high-quality RHE. Overall, our results suggest that improving mitochondrial function in KiPS is one of the key aspects to obtain a functional RHE and that our plant extracts can improve in this process. |
format | Online Article Text |
id | pubmed-9156774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91567742022-06-02 Reconstruction of functional human epidermis equivalent containing 5%IPS-derived keratinocytes treated with mitochondrial stimulating plant extracts Moreau, Marielle Capallere, Christophe Chavatte, Laurent Plaza, Christelle Meyrignac, Céline Pays, Karl Bavouzet, Bruno Botto, Jean-Marie Nizard, Carine Bulteau, Anne-Laure Sci Rep Article Reconstructed human epidermis equivalents (RHE) have been developed as a clinical skin substitute and as the replacement for animal testing in both research and industry. KiPS, or keratinocytes derived from induced pluripotent stem cells (iPSCs) are frequently used to generate RHE. In this study, we focus on the mitochondrial performance of the KiPS derived from iPSCs obtained from two donors. We found that the KiPS derived from the older donor have more defective mitochondria. Treatment of these KiPS with a plant extract enriched in compounds known to protect mitochondria improved mitochondrial respiration and rendered them fully competent to derive high-quality RHE. Overall, our results suggest that improving mitochondrial function in KiPS is one of the key aspects to obtain a functional RHE and that our plant extracts can improve in this process. Nature Publishing Group UK 2022-05-31 /pmc/articles/PMC9156774/ /pubmed/35641783 http://dx.doi.org/10.1038/s41598-022-13191-4 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Moreau, Marielle Capallere, Christophe Chavatte, Laurent Plaza, Christelle Meyrignac, Céline Pays, Karl Bavouzet, Bruno Botto, Jean-Marie Nizard, Carine Bulteau, Anne-Laure Reconstruction of functional human epidermis equivalent containing 5%IPS-derived keratinocytes treated with mitochondrial stimulating plant extracts |
title | Reconstruction of functional human epidermis equivalent containing 5%IPS-derived keratinocytes treated with mitochondrial stimulating plant extracts |
title_full | Reconstruction of functional human epidermis equivalent containing 5%IPS-derived keratinocytes treated with mitochondrial stimulating plant extracts |
title_fullStr | Reconstruction of functional human epidermis equivalent containing 5%IPS-derived keratinocytes treated with mitochondrial stimulating plant extracts |
title_full_unstemmed | Reconstruction of functional human epidermis equivalent containing 5%IPS-derived keratinocytes treated with mitochondrial stimulating plant extracts |
title_short | Reconstruction of functional human epidermis equivalent containing 5%IPS-derived keratinocytes treated with mitochondrial stimulating plant extracts |
title_sort | reconstruction of functional human epidermis equivalent containing 5%ips-derived keratinocytes treated with mitochondrial stimulating plant extracts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156774/ https://www.ncbi.nlm.nih.gov/pubmed/35641783 http://dx.doi.org/10.1038/s41598-022-13191-4 |
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