Cargando…

3D artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions

In the context of xenotransplantation, in ischemia/reperfusion injury as well as in cardiovascular research, the study of the fascinating interplay between endothelial cells (EC) and the plasma cascade systems often requires in vitro models. Blood vessels are hardly reproducible with standard flat-b...

Descripción completa

Detalles Bibliográficos
Autores principales: Sfriso, Riccardo, Zhang, Shengye, Bichsel, Colette Andrea, Steck, Oliver, Despont, Alain, Guenat, Olivier Thierry, Rieben, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897395/
https://www.ncbi.nlm.nih.gov/pubmed/29651108
http://dx.doi.org/10.1038/s41598-018-24273-7
_version_ 1783313949744168960
author Sfriso, Riccardo
Zhang, Shengye
Bichsel, Colette Andrea
Steck, Oliver
Despont, Alain
Guenat, Olivier Thierry
Rieben, Robert
author_facet Sfriso, Riccardo
Zhang, Shengye
Bichsel, Colette Andrea
Steck, Oliver
Despont, Alain
Guenat, Olivier Thierry
Rieben, Robert
author_sort Sfriso, Riccardo
collection PubMed
description In the context of xenotransplantation, in ischemia/reperfusion injury as well as in cardiovascular research, the study of the fascinating interplay between endothelial cells (EC) and the plasma cascade systems often requires in vitro models. Blood vessels are hardly reproducible with standard flat-bed culture systems and flow-plate assays are limited in their low surface-to-volume ratio which impedes the study of the anticoagulant properties of the endothelial cells. According to the 3R regulations (reduce, replace and refine animal experimentation) we developed a closed circuit microfluidic in vitro system in which endothelial cells are cultured in 3D round section microchannels and subjected to physiological, pulsatile flow. In this study, a 3D monolayer of porcine aortic EC was perfused with human serum to mimic a xenotransplantation setting. Complement as well as EC activation was assessed in the presence or absence of complement inhibitors showing the versatility of the model for drug testing. Complement activation products as well as E-selectin expression were detected and visualized in situ by high resolution confocal microscopy. Furthermore, porcine pro-inflammatory cytokines as well as soluble complement components in the recirculating fluid phase were detected after human serum perfusion providing a better overview of the artificial vascular environment.
format Online
Article
Text
id pubmed-5897395
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-58973952018-04-20 3D artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions Sfriso, Riccardo Zhang, Shengye Bichsel, Colette Andrea Steck, Oliver Despont, Alain Guenat, Olivier Thierry Rieben, Robert Sci Rep Article In the context of xenotransplantation, in ischemia/reperfusion injury as well as in cardiovascular research, the study of the fascinating interplay between endothelial cells (EC) and the plasma cascade systems often requires in vitro models. Blood vessels are hardly reproducible with standard flat-bed culture systems and flow-plate assays are limited in their low surface-to-volume ratio which impedes the study of the anticoagulant properties of the endothelial cells. According to the 3R regulations (reduce, replace and refine animal experimentation) we developed a closed circuit microfluidic in vitro system in which endothelial cells are cultured in 3D round section microchannels and subjected to physiological, pulsatile flow. In this study, a 3D monolayer of porcine aortic EC was perfused with human serum to mimic a xenotransplantation setting. Complement as well as EC activation was assessed in the presence or absence of complement inhibitors showing the versatility of the model for drug testing. Complement activation products as well as E-selectin expression were detected and visualized in situ by high resolution confocal microscopy. Furthermore, porcine pro-inflammatory cytokines as well as soluble complement components in the recirculating fluid phase were detected after human serum perfusion providing a better overview of the artificial vascular environment. Nature Publishing Group UK 2018-04-12 /pmc/articles/PMC5897395/ /pubmed/29651108 http://dx.doi.org/10.1038/s41598-018-24273-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sfriso, Riccardo
Zhang, Shengye
Bichsel, Colette Andrea
Steck, Oliver
Despont, Alain
Guenat, Olivier Thierry
Rieben, Robert
3D artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions
title 3D artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions
title_full 3D artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions
title_fullStr 3D artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions
title_full_unstemmed 3D artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions
title_short 3D artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions
title_sort 3d artificial round section micro-vessels to investigate endothelial cells under physiological flow conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897395/
https://www.ncbi.nlm.nih.gov/pubmed/29651108
http://dx.doi.org/10.1038/s41598-018-24273-7
work_keys_str_mv AT sfrisoriccardo 3dartificialroundsectionmicrovesselstoinvestigateendothelialcellsunderphysiologicalflowconditions
AT zhangshengye 3dartificialroundsectionmicrovesselstoinvestigateendothelialcellsunderphysiologicalflowconditions
AT bichselcoletteandrea 3dartificialroundsectionmicrovesselstoinvestigateendothelialcellsunderphysiologicalflowconditions
AT steckoliver 3dartificialroundsectionmicrovesselstoinvestigateendothelialcellsunderphysiologicalflowconditions
AT despontalain 3dartificialroundsectionmicrovesselstoinvestigateendothelialcellsunderphysiologicalflowconditions
AT guenatolivierthierry 3dartificialroundsectionmicrovesselstoinvestigateendothelialcellsunderphysiologicalflowconditions
AT riebenrobert 3dartificialroundsectionmicrovesselstoinvestigateendothelialcellsunderphysiologicalflowconditions