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Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro
Chronic wounds, such as leg ulcers associated with sickle cell disease, occur as a consequence of a prolonged inflammatory phase during the healing process. They are extremely hard to heal and persist as a significant health care problem due to the absence of effective treatment and the uprising num...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998132/ https://www.ncbi.nlm.nih.gov/pubmed/35406716 http://dx.doi.org/10.3390/cells11071151 |
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author | Domingues, Sophie Darle, Annabelle Masson, Yolande Saidani, Manoubia Lagoutte, Emilie Bejanariu, Ana Coutier, Julien Ayata, Raif Eren Bouschbacher, Marielle Peschanski, Marc Lemaitre, Gilles Baldeschi, Christine |
author_facet | Domingues, Sophie Darle, Annabelle Masson, Yolande Saidani, Manoubia Lagoutte, Emilie Bejanariu, Ana Coutier, Julien Ayata, Raif Eren Bouschbacher, Marielle Peschanski, Marc Lemaitre, Gilles Baldeschi, Christine |
author_sort | Domingues, Sophie |
collection | PubMed |
description | Chronic wounds, such as leg ulcers associated with sickle cell disease, occur as a consequence of a prolonged inflammatory phase during the healing process. They are extremely hard to heal and persist as a significant health care problem due to the absence of effective treatment and the uprising number of patients. Indeed, there is a critical need to develop novel cell- and tissue-based therapies to treat these chronic wounds. Development in skin engineering leads to a small catalogue of available substitutes manufactured in Good Manufacturing Practices compliant (GMPc) conditions. Those substitutes are produced using primary cells that could limit their use due to restricted sourcing. Here, we propose GMPc protocols to produce functional populations of keratinocytes and fibroblasts derived from pluripotent stem cells to reconstruct the associated dermo-epidermal substitute with plasma-based fibrin matrix. In addition, this manufactured composite skin is biologically active and enhances in vitro wounding of keratinocytes. The proposed composite skin opens new perspectives for skin replacement using allogeneic substitute. |
format | Online Article Text |
id | pubmed-8998132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89981322022-04-12 Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro Domingues, Sophie Darle, Annabelle Masson, Yolande Saidani, Manoubia Lagoutte, Emilie Bejanariu, Ana Coutier, Julien Ayata, Raif Eren Bouschbacher, Marielle Peschanski, Marc Lemaitre, Gilles Baldeschi, Christine Cells Article Chronic wounds, such as leg ulcers associated with sickle cell disease, occur as a consequence of a prolonged inflammatory phase during the healing process. They are extremely hard to heal and persist as a significant health care problem due to the absence of effective treatment and the uprising number of patients. Indeed, there is a critical need to develop novel cell- and tissue-based therapies to treat these chronic wounds. Development in skin engineering leads to a small catalogue of available substitutes manufactured in Good Manufacturing Practices compliant (GMPc) conditions. Those substitutes are produced using primary cells that could limit their use due to restricted sourcing. Here, we propose GMPc protocols to produce functional populations of keratinocytes and fibroblasts derived from pluripotent stem cells to reconstruct the associated dermo-epidermal substitute with plasma-based fibrin matrix. In addition, this manufactured composite skin is biologically active and enhances in vitro wounding of keratinocytes. The proposed composite skin opens new perspectives for skin replacement using allogeneic substitute. MDPI 2022-03-29 /pmc/articles/PMC8998132/ /pubmed/35406716 http://dx.doi.org/10.3390/cells11071151 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Domingues, Sophie Darle, Annabelle Masson, Yolande Saidani, Manoubia Lagoutte, Emilie Bejanariu, Ana Coutier, Julien Ayata, Raif Eren Bouschbacher, Marielle Peschanski, Marc Lemaitre, Gilles Baldeschi, Christine Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro |
title | Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro |
title_full | Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro |
title_fullStr | Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro |
title_full_unstemmed | Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro |
title_short | Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro |
title_sort | clinical grade human pluripotent stem cell-derived engineered skin substitutes promote keratinocytes wound closure in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998132/ https://www.ncbi.nlm.nih.gov/pubmed/35406716 http://dx.doi.org/10.3390/cells11071151 |
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