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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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