Radial matrix constraint influences tissue contraction and promotes maturation of bi-layered skin equivalents.

3D-printed culture system Collagen hydrogel Extracellular matrix production Finite element simulation In vitro human skin equivalent Keratinocyte differentiation Mechanical stimulus Radial matrix constraint Tissue organization

Journal

Biomaterials advances
ISSN: 2772-9508
Titre abrégé: Biomater Adv
Pays: Netherlands
ID NLM: 9918383886206676

Informations de publication

Date de publication:
14 Nov 2023
Historique:
received: 10 05 2023
revised: 26 10 2023
accepted: 12 11 2023
medline: 23 11 2023
pubmed: 23 11 2023
entrez: 22 11 2023
Statut: aheadofprint

Résumé

Human skin equivalents (HSEs) serve as important tools for mechanistic studies with human skin cells, drug discovery, pre-clinical applications in the field of tissue engineering and for skin transplantation on skin defects. Besides the cellular and extracellular matrix (ECM) components used for HSEs, physical constraints applied on the scaffold during HSEs maturation influence tissue organization, functionality, and homogeneity. In this study, we introduce a 3D-printed culture insert that exposes bi-layered HSEs to a static radial constraint through matrix adhesion. We examine the effect of various diameters of the ring-shaped culture insert on the HSE's characteristics and compare them to state-of-the-art unconstrained and planar constrained HSEs. We show that radial matrix constraint of HSEs regulates tissue contraction, promotes fibroblast and matrix organization that is similar to human skin in vivo and improves keratinocyte differentiation, epidermal stratification, and basement membrane formation depending on the culture insert diameter. Together, these data demonstrate that the degree of HSE's contraction is an important design consideration in skin tissue engineering. Therefore, this study can help to mimic various in vivo skin conditions and to increase the control of relevant tissue properties.

Identifiants

pubmed: 37992477
pii: S2772-9508(23)00425-9
doi: 10.1016/j.bioadv.2023.213702
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

213702

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Jessica Polak (J)

Department of Mechanical and Process Engineering, ETH Zurich, Zurich 8092, Switzerland. Electronic address: jessica.polak@gmail.com.

David Sachs (D)

Department of Mechanical and Process Engineering, ETH Zurich, Zurich 8092, Switzerland.

Nino Scherrer (N)

Department of Computer Science, ETH Zurich, Zurich 8092, Switzerland.

Adrian Süess (A)

Department of Mechanical and Process Engineering, ETH Zurich, Zurich 8092, Switzerland.

Huan Liu (H)

Institute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich 8093, Switzerland.

Mitchell Levesque (M)

Department of Dermatology, University Hospital Zurich, Zurich 8091, Switzerland.

Sabine Werner (S)

Institute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich 8093, Switzerland.

Edoardo Mazza (E)

Department of Mechanical and Process Engineering, ETH Zurich, Zurich 8092, Switzerland; Swiss Federal Laboratories for Materials Science and Technology (EMPA), Dubendorf 8600, Switzerland.

Gaetana Restivo (G)

Department of Dermatology, University Hospital Zurich, Zurich 8091, Switzerland.

Mirko Meboldt (M)

Department of Mechanical and Process Engineering, ETH Zurich, Zurich 8092, Switzerland.

Costanza Giampietro (C)

Department of Mechanical and Process Engineering, ETH Zurich, Zurich 8092, Switzerland; Swiss Federal Laboratories for Materials Science and Technology (EMPA), Dubendorf 8600, Switzerland.

Classifications MeSH