Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro.

GMP compliant fibroblasts keratinocytes pluripotent stem cells skin tissue engineering wound healing

Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
29 03 2022
Historique:
received: 02 02 2022
revised: 21 03 2022
accepted: 24 03 2022
entrez: 12 4 2022
pubmed: 13 4 2022
medline: 14 4 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 35406716
pii: cells11071151
doi: 10.3390/cells11071151
pmc: PMC8998132
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Sophie Domingues (S)

Centre d'Etude des Cellules Souches, 91100 Corbeil-Essonnes, France.

Annabelle Darle (A)

Centre d'Etude des Cellules Souches, 91100 Corbeil-Essonnes, France.

Yolande Masson (Y)

Centre d'Etude des Cellules Souches, 91100 Corbeil-Essonnes, France.

Manoubia Saidani (M)

Centre d'Etude des Cellules Souches, 91100 Corbeil-Essonnes, France.

Emilie Lagoutte (E)

URGO RID, 42 Rue de Longvic, 21300 Chenôve, France.

Ana Bejanariu (A)

Centre d'Etude des Cellules Souches, 91100 Corbeil-Essonnes, France.

Julien Coutier (J)

Centre d'Etude des Cellules Souches, 91100 Corbeil-Essonnes, France.

Raif Eren Ayata (RE)

INSERM U861, I-Stem, AFM, Institute for Stem Cell Therapy and Exploration of Monogenic Diseases, 91100 Corbeil-Essonnes, France.
Université Paris-Saclay, Université d'Evry, U861, 91100 Corbeil-Essonnes, France.

Marielle Bouschbacher (M)

URGO RID, 42 Rue de Longvic, 21300 Chenôve, France.

Marc Peschanski (M)

Centre d'Etude des Cellules Souches, 91100 Corbeil-Essonnes, France.

Gilles Lemaitre (G)

INSERM U861, I-Stem, AFM, Institute for Stem Cell Therapy and Exploration of Monogenic Diseases, 91100 Corbeil-Essonnes, France.
Université Paris-Saclay, Université d'Evry, U861, 91100 Corbeil-Essonnes, France.

Christine Baldeschi (C)

INSERM U861, I-Stem, AFM, Institute for Stem Cell Therapy and Exploration of Monogenic Diseases, 91100 Corbeil-Essonnes, France.
Université Paris-Saclay, Université d'Evry, U861, 91100 Corbeil-Essonnes, France.

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