Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro

Abstract The integration of metabolic competence in developmental toxicity assays in vitro is of fundamental importance to better predict adverse drug effects. Here, a microfluidic hanging‐drop platform is presented that seamlessly integrates liver metabolism into the embryonic stem cell test (EST)....

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Main Authors: Julia Alicia Boos, Patrick Mark Misun, Astrid Michlmayr, Andreas Hierlemann, Olivier Frey
Format: Article
Language:English
Published: Wiley 2019-07-01
Series:Advanced Science
Subjects:
Online Access:https://doi.org/10.1002/advs.201900294
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spelling doaj-cd856205f3d740beaa251331be29a2942020-11-24T21:27:38ZengWileyAdvanced Science2198-38442019-07-01613n/an/a10.1002/advs.201900294Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In VitroJulia Alicia Boos0Patrick Mark Misun1Astrid Michlmayr2Andreas Hierlemann3Olivier Frey4Bioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandBioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandBioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandBioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandBioengineering Laboratory Department of Biosystems Science and Engineering ETH Zürich Mattenstrasse 26 4058 Basel SwitzerlandAbstract The integration of metabolic competence in developmental toxicity assays in vitro is of fundamental importance to better predict adverse drug effects. Here, a microfluidic hanging‐drop platform is presented that seamlessly integrates liver metabolism into the embryonic stem cell test (EST). Primary human liver microtissues (hLiMTs) and embryoid bodies (EBs) are combined in the same fluidic network, so that hLiMT‐generated metabolites are directly transported to the EBs. Gravity‐driven flow through the network enables continuous intertissue communication, constant medium turnover, and, most importantly, immediate exchange of metabolites. As a proof of concept, the prodrug cyclophosphamide is investigated and a fourfold lower ID50 concentration (50% inhibition of EB differentiation) is found after biotransformation, which demonstrates the potentially adverse effects of metabolites on embryotoxicity. The metaEST platform provides a promising tool to increase the predictive power of the current EST assay by more comprehensively including and better reflecting physiological processes in in vitro tests.https://doi.org/10.1002/advs.2019002943D microtissuesbody‐on‐a‐chipdevelopmental toxicityembryonic stem cell testsmicrofluidics
collection DOAJ
language English
format Article
sources DOAJ
author Julia Alicia Boos
Patrick Mark Misun
Astrid Michlmayr
Andreas Hierlemann
Olivier Frey
spellingShingle Julia Alicia Boos
Patrick Mark Misun
Astrid Michlmayr
Andreas Hierlemann
Olivier Frey
Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro
Advanced Science
3D microtissues
body‐on‐a‐chip
developmental toxicity
embryonic stem cell tests
microfluidics
author_facet Julia Alicia Boos
Patrick Mark Misun
Astrid Michlmayr
Andreas Hierlemann
Olivier Frey
author_sort Julia Alicia Boos
title Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro
title_short Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro
title_full Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro
title_fullStr Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro
title_full_unstemmed Microfluidic Multitissue Platform for Advanced Embryotoxicity Testing In Vitro
title_sort microfluidic multitissue platform for advanced embryotoxicity testing in vitro
publisher Wiley
series Advanced Science
issn 2198-3844
publishDate 2019-07-01
description Abstract The integration of metabolic competence in developmental toxicity assays in vitro is of fundamental importance to better predict adverse drug effects. Here, a microfluidic hanging‐drop platform is presented that seamlessly integrates liver metabolism into the embryonic stem cell test (EST). Primary human liver microtissues (hLiMTs) and embryoid bodies (EBs) are combined in the same fluidic network, so that hLiMT‐generated metabolites are directly transported to the EBs. Gravity‐driven flow through the network enables continuous intertissue communication, constant medium turnover, and, most importantly, immediate exchange of metabolites. As a proof of concept, the prodrug cyclophosphamide is investigated and a fourfold lower ID50 concentration (50% inhibition of EB differentiation) is found after biotransformation, which demonstrates the potentially adverse effects of metabolites on embryotoxicity. The metaEST platform provides a promising tool to increase the predictive power of the current EST assay by more comprehensively including and better reflecting physiological processes in in vitro tests.
topic 3D microtissues
body‐on‐a‐chip
developmental toxicity
embryonic stem cell tests
microfluidics
url https://doi.org/10.1002/advs.201900294
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