Angiogenesis and full thickness wound repair in a cell sheet-based vascularized skin substitute.

Skin tissue engineering cell sheet matrix microenvironment vascularization wound repair

Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
23 Aug 2024
Historique:
received: 15 03 2024
revised: 05 08 2024
accepted: 16 08 2024
medline: 26 8 2024
pubmed: 26 8 2024
entrez: 25 8 2024
Statut: aheadofprint

Résumé

Skin tissue engineering is undergoing tremendous expansion as a result from clinical needs, mandatory replacement of animal models and development of new technologies. Many approaches have been used to produce vascularized skin substitutes for grafting purposes showing the presence of capillary-like structures but with limited analysis of their in vitro maturation and plasticity. Such knowledge is however important for the development of tissue substitutes with improved implantation success as well as for validation of vascularization in in vitro models, including as a readout in pharmacological analyses. For optimal interactions of cells with microenvironment and vasculature, we here used a cell sheet approach consisting in the sole production of matrix by the cells. In this context, we limited the density of endothelial cells seeded for self-assembly and rather relied on the stimulation of angiogenesis for the development of an extensive connected microvascular-like network. After detailed characterization of this network, we challenged its plasticity both during and after establishment of the skin substitute. We show that fine tuning of VEGF concentration and time of application differentially affects formation of capillary-like structures and their perivascular coverage. Furthermore, we performed a deep wound assay that displayed tissue repair and angiogenesis with unique characteristics of the physiological process. These studies demonstrate the importance of cell-derived microenvironment for the establishment of mature yet dynamic vascularized skin models allowing a wide range of pharmacological and basic investigations. STATEMENT OF SIGNIFICANCE: The significant advancements in organ-on-chips and tissue engineering call for more relevant models including microvascularization with remodeling potential. While vascularized skin substitutes have been developed for years, focus has primarily been on the impact of microvascularization on implantation rather than on its in vitro characterization. We here developed a cell sheet-based vascularized skin substitute relying on angiogenesis, i.e. growth of vessel-like structures within the 3D model, rather than solely on endothelial cell self-assembly. We then characterized : -1/ vascularization after modulation of angiogenic factor VEGF during the substitute construction; -2/ angiogenesis associated to tissue repair after deep mechanical wounding. These studies establish a solid physiologically relevant model for further investigation of skin cell interactions and in vitro wound healing.

Identifiants

pubmed: 39182802
pii: S1742-7061(24)00466-5
doi: 10.1016/j.actbio.2024.08.023
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Adèle Mauroux, Sandrine Gofflo, Josselin Breugnot, Laëtitia Marchand, Sylvie Bordes, and Brigitte Closs are employees of SILAB. Florence Ruggiero and Laurent Muller declare the receipt of a grant from SILAB. MM, YA, CAR, PM, CM and SG state no conflict of interest

Auteurs

Adèle Mauroux (A)

Center for Interdisciplinary Research in Biology (CIRB), College de France - CNRS, INSERM, Université PSL, 11 Place Marcelin Berthelot, 75005 Paris, France; R&D Department, SILAB, ZI de la Nau, 19240 Saint Viance, France; Institut de Génomique Fonctionnelle de Lyon (IGFL), ENS de Lyon, CNRS, Univ Lyon 1, 32-34 Avenue Tony Garnier, 69007 Lyon, France; Sorbonne Université, Collège doctoral, 15 rue de l'Ecole de Médecine, 75006 Paris, France.

Sandrine Gofflo (S)

R&D Department, SILAB, ZI de la Nau, 19240 Saint Viance, France.

Josselin Breugnot (J)

R&D Department, SILAB, ZI de la Nau, 19240 Saint Viance, France.

Marilyne Malbouyres (M)

Institut de Génomique Fonctionnelle de Lyon (IGFL), ENS de Lyon, CNRS, Univ Lyon 1, 32-34 Avenue Tony Garnier, 69007 Lyon, France.

Yoann Atlas (Y)

Center for Interdisciplinary Research in Biology (CIRB), College de France - CNRS, INSERM, Université PSL, 11 Place Marcelin Berthelot, 75005 Paris, France; Sorbonne Université, Collège doctoral, 15 rue de l'Ecole de Médecine, 75006 Paris, France.

Corinne Ardidie-Robouant (C)

Center for Interdisciplinary Research in Biology (CIRB), College de France - CNRS, INSERM, Université PSL, 11 Place Marcelin Berthelot, 75005 Paris, France.

Laëtitia Marchand (L)

R&D Department, SILAB, ZI de la Nau, 19240 Saint Viance, France.

Catherine Monnot (C)

Center for Interdisciplinary Research in Biology (CIRB), College de France - CNRS, INSERM, Université PSL, 11 Place Marcelin Berthelot, 75005 Paris, France.

Stéphane Germain (S)

Center for Interdisciplinary Research in Biology (CIRB), College de France - CNRS, INSERM, Université PSL, 11 Place Marcelin Berthelot, 75005 Paris, France.

Sylvie Bordes (S)

R&D Department, SILAB, ZI de la Nau, 19240 Saint Viance, France.

Brigitte Closs (B)

R&D Department, SILAB, ZI de la Nau, 19240 Saint Viance, France.

Florence Ruggiero (F)

Institut de Génomique Fonctionnelle de Lyon (IGFL), ENS de Lyon, CNRS, Univ Lyon 1, 32-34 Avenue Tony Garnier, 69007 Lyon, France.

Laurent Muller (L)

Center for Interdisciplinary Research in Biology (CIRB), College de France - CNRS, INSERM, Université PSL, 11 Place Marcelin Berthelot, 75005 Paris, France. Electronic address: laurent.muller@college-de-france.fr.

Classifications MeSH