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A Novel Bioreactor System for the Assessment of Endothelialization on Deformable Surfaces

The generation of a living protective layer at the luminal surface of cardiovascular devices, composed of an autologous functional endothelium, represents the ideal solution to life-threatening, implant-related complications in cardiovascular patients. The initial evaluation of engineering strategie...

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Autores principales: Bachmann, Björn J., Bernardi, Laura, Loosli, Christian, Marschewski, Julian, Perrini, Michela, Ehrbar, Martin, Ermanni, Paolo, Poulikakos, Dimos, Ferrari, Aldo, Mazza, Edoardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5150819/
https://www.ncbi.nlm.nih.gov/pubmed/27941901
http://dx.doi.org/10.1038/srep38861
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author Bachmann, Björn J.
Bernardi, Laura
Loosli, Christian
Marschewski, Julian
Perrini, Michela
Ehrbar, Martin
Ermanni, Paolo
Poulikakos, Dimos
Ferrari, Aldo
Mazza, Edoardo
author_facet Bachmann, Björn J.
Bernardi, Laura
Loosli, Christian
Marschewski, Julian
Perrini, Michela
Ehrbar, Martin
Ermanni, Paolo
Poulikakos, Dimos
Ferrari, Aldo
Mazza, Edoardo
author_sort Bachmann, Björn J.
collection PubMed
description The generation of a living protective layer at the luminal surface of cardiovascular devices, composed of an autologous functional endothelium, represents the ideal solution to life-threatening, implant-related complications in cardiovascular patients. The initial evaluation of engineering strategies fostering endothelial cell adhesion and proliferation as well as the long-term tissue homeostasis requires in vitro testing in environmental model systems able to recapitulate the hemodynamic conditions experienced at the blood-to-device interface of implants as well as the substrate deformation. Here, we introduce the design and validation of a novel bioreactor system which enables the long-term conditioning of human endothelial cells interacting with artificial materials under dynamic combinations of flow-generated wall shear stress and wall deformation. The wall shear stress and wall deformation values obtained encompass both the physiological and supraphysiological range. They are determined through separate actuation systems which are controlled based on validated computational models. In addition, we demonstrate the good optical conductivity of the system permitting online monitoring of cell activities through live-cell imaging as well as standard biochemical post-processing. Altogether, the bioreactor system defines an unprecedented testing hub for potential strategies toward the endothelialization or re-endothelialization of target substrates.
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spelling pubmed-51508192016-12-19 A Novel Bioreactor System for the Assessment of Endothelialization on Deformable Surfaces Bachmann, Björn J. Bernardi, Laura Loosli, Christian Marschewski, Julian Perrini, Michela Ehrbar, Martin Ermanni, Paolo Poulikakos, Dimos Ferrari, Aldo Mazza, Edoardo Sci Rep Article The generation of a living protective layer at the luminal surface of cardiovascular devices, composed of an autologous functional endothelium, represents the ideal solution to life-threatening, implant-related complications in cardiovascular patients. The initial evaluation of engineering strategies fostering endothelial cell adhesion and proliferation as well as the long-term tissue homeostasis requires in vitro testing in environmental model systems able to recapitulate the hemodynamic conditions experienced at the blood-to-device interface of implants as well as the substrate deformation. Here, we introduce the design and validation of a novel bioreactor system which enables the long-term conditioning of human endothelial cells interacting with artificial materials under dynamic combinations of flow-generated wall shear stress and wall deformation. The wall shear stress and wall deformation values obtained encompass both the physiological and supraphysiological range. They are determined through separate actuation systems which are controlled based on validated computational models. In addition, we demonstrate the good optical conductivity of the system permitting online monitoring of cell activities through live-cell imaging as well as standard biochemical post-processing. Altogether, the bioreactor system defines an unprecedented testing hub for potential strategies toward the endothelialization or re-endothelialization of target substrates. Nature Publishing Group 2016-12-12 /pmc/articles/PMC5150819/ /pubmed/27941901 http://dx.doi.org/10.1038/srep38861 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Bachmann, Björn J.
Bernardi, Laura
Loosli, Christian
Marschewski, Julian
Perrini, Michela
Ehrbar, Martin
Ermanni, Paolo
Poulikakos, Dimos
Ferrari, Aldo
Mazza, Edoardo
A Novel Bioreactor System for the Assessment of Endothelialization on Deformable Surfaces
title A Novel Bioreactor System for the Assessment of Endothelialization on Deformable Surfaces
title_full A Novel Bioreactor System for the Assessment of Endothelialization on Deformable Surfaces
title_fullStr A Novel Bioreactor System for the Assessment of Endothelialization on Deformable Surfaces
title_full_unstemmed A Novel Bioreactor System for the Assessment of Endothelialization on Deformable Surfaces
title_short A Novel Bioreactor System for the Assessment of Endothelialization on Deformable Surfaces
title_sort novel bioreactor system for the assessment of endothelialization on deformable surfaces
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5150819/
https://www.ncbi.nlm.nih.gov/pubmed/27941901
http://dx.doi.org/10.1038/srep38861
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