Micropattern-based platform as a physiologically relevant model to study epithelial morphogenesis and nephrotoxicity.


Journal

Biomaterials
ISSN: 1878-5905
Titre abrégé: Biomaterials
Pays: Netherlands
ID NLM: 8100316

Informations de publication

Date de publication:
10 2019
Historique:
received: 16 11 2018
revised: 04 07 2019
accepted: 05 07 2019
pubmed: 22 7 2019
medline: 22 9 2020
entrez: 22 7 2019
Statut: ppublish

Résumé

Tubulogenesis in epithelial organs often initiates with the acquisition of apicobasal polarity, giving rise to the formation of small lumens that expand and fuse to generate a single opened cavity. In this study, we present a micropattern-based device engineered to generate epithelial tubes through a process that recapitulates in vivo tubule morphogenesis. Interestingly, tubulogenesis in this device is dependent on microenvironmental cues such as cell confinement, extracellular matrix composition, and substrate stiffness, and our set-up specifically allows the control of these extracellular conditions. Additionally, proximal tubule cell lines growing on micropatterns express higher levels of drug transporters and are more sensitive to nephrotoxicity. These tubes display specific morphological defects that can be linked to nephrotoxicity, which would be helpful to predict potential toxicity when developing new compounds. This device, with the ability to recapitulate tube formation in vitro, has emerged as a powerful tool to study the molecular mechanisms involved in organogenesis and, by being more physiologically relevant than existing cellular models, becomes an innovative platform to conduct drug discovery assays.

Identifiants

pubmed: 31326655
pii: S0142-9612(19)30438-7
doi: 10.1016/j.biomaterials.2019.119339
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

119339

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Minerva Bosch-Fortea (M)

Department of Development and Regeneration, Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Madrid, Spain; Institute of Bioengineering and School of Engineering and Materials Science, Queen Mary University of London, London, UK.

Alejo E Rodriguez-Fraticelli (AE)

Department of Development and Regeneration, Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Madrid, Spain; Stem Cell Program and Dept. of Hematology/Oncology, Boston Children's Hospital, Boston, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, USA; Dept. of Pediatrics, Harvard Medical School, Boston, USA.

Gonzalo Herranz (G)

Department of Development and Regeneration, Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Madrid, Spain.

Mariam Hachimi (M)

Department of Development and Regeneration, Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Madrid, Spain; Stem Cell Program and Dept. of Hematology/Oncology, Boston Children's Hospital, Boston, USA; Dept. of Pathology, Harvard Medical School, Boston, USA.

Maria D Barea (MD)

Department of Development and Regeneration, Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Madrid, Spain.

Joanne Young (J)

CYTOO SA, Minatec, Grenoble, France.

Benoit Ladoux (B)

Institut Jacques Monod (IJM), Centre National de la Recherche Scientifique (CNRS) Unité Mixte de Recherche (UMR) and Université Paris Diderot, Paris, France; Mechanobiology Institute, National University of Singapore, Singapore.

Fernando Martin-Belmonte (F)

Department of Development and Regeneration, Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Madrid, Spain. Electronic address: fmartin@cbm.csic.es.

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