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Fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities

Over the last decade, Organ-on-Chip (OoC) emerged as a promising technology for advanced in vitro models, recapitulating key physiological cues. OoC approaches tailored for cardiac tissue engineering resulted in a variety of platforms, some of which integrate stimulation or probing capabilities. Due...

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Detalles Bibliográficos
Autores principales: Schneider, Oliver, Moruzzi, Alessia, Fuchs, Stefanie, Grobel, Alina, Schulze, Henrike S., Mayr, Torsten, Loskill, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120495/
https://www.ncbi.nlm.nih.gov/pubmed/35601892
http://dx.doi.org/10.1016/j.mtbio.2022.100280
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author Schneider, Oliver
Moruzzi, Alessia
Fuchs, Stefanie
Grobel, Alina
Schulze, Henrike S.
Mayr, Torsten
Loskill, Peter
author_facet Schneider, Oliver
Moruzzi, Alessia
Fuchs, Stefanie
Grobel, Alina
Schulze, Henrike S.
Mayr, Torsten
Loskill, Peter
author_sort Schneider, Oliver
collection PubMed
description Over the last decade, Organ-on-Chip (OoC) emerged as a promising technology for advanced in vitro models, recapitulating key physiological cues. OoC approaches tailored for cardiac tissue engineering resulted in a variety of platforms, some of which integrate stimulation or probing capabilities. Due to manual handling processes, however, a large-scale standardized and robust tissue generation, applicable in an industrial setting, is still out of reach. Here, we present a novel cell injection and tissue generation concept relying on spheroids, which can be produced in large quantities and uniform size from induced pluripotent stem cell-derived human cardiomyocytes. Hydrostatic flow transports and accumulates spheroids in dogbone-shaped tissue chambers, which subsequently fuse and form aligned, contracting cardiac muscle fibers. Furthermore, we demonstrate electrical stimulation capabilities by utilizing fluidic media connectors as electrodes and provide the blueprint of a low-cost, open-source, scriptable pulse generator. We report on a novel integration strategy of optical O(2) sensor spots into resin-based microfluidic systems, enabling in situ determination of O(2) partial pressures. Finally, a proof-of-concept demonstrating electrical stimulation combined with in situ monitoring of metabolic activity in cardiac tissues is provided. The developed system thus opens the door for advanced OoCs integrating biophysical stimulation as well as probing capabilities and serves as a blueprint for the facile and robust generation of high density microtissues in microfluidic modules amenable to scaling-up and automation.
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spelling pubmed-91204952022-05-21 Fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities Schneider, Oliver Moruzzi, Alessia Fuchs, Stefanie Grobel, Alina Schulze, Henrike S. Mayr, Torsten Loskill, Peter Mater Today Bio Full Length Article Over the last decade, Organ-on-Chip (OoC) emerged as a promising technology for advanced in vitro models, recapitulating key physiological cues. OoC approaches tailored for cardiac tissue engineering resulted in a variety of platforms, some of which integrate stimulation or probing capabilities. Due to manual handling processes, however, a large-scale standardized and robust tissue generation, applicable in an industrial setting, is still out of reach. Here, we present a novel cell injection and tissue generation concept relying on spheroids, which can be produced in large quantities and uniform size from induced pluripotent stem cell-derived human cardiomyocytes. Hydrostatic flow transports and accumulates spheroids in dogbone-shaped tissue chambers, which subsequently fuse and form aligned, contracting cardiac muscle fibers. Furthermore, we demonstrate electrical stimulation capabilities by utilizing fluidic media connectors as electrodes and provide the blueprint of a low-cost, open-source, scriptable pulse generator. We report on a novel integration strategy of optical O(2) sensor spots into resin-based microfluidic systems, enabling in situ determination of O(2) partial pressures. Finally, a proof-of-concept demonstrating electrical stimulation combined with in situ monitoring of metabolic activity in cardiac tissues is provided. The developed system thus opens the door for advanced OoCs integrating biophysical stimulation as well as probing capabilities and serves as a blueprint for the facile and robust generation of high density microtissues in microfluidic modules amenable to scaling-up and automation. Elsevier 2022-05-07 /pmc/articles/PMC9120495/ /pubmed/35601892 http://dx.doi.org/10.1016/j.mtbio.2022.100280 Text en © 2022 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Schneider, Oliver
Moruzzi, Alessia
Fuchs, Stefanie
Grobel, Alina
Schulze, Henrike S.
Mayr, Torsten
Loskill, Peter
Fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities
title Fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities
title_full Fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities
title_fullStr Fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities
title_full_unstemmed Fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities
title_short Fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities
title_sort fusing spheroids to aligned μ-tissues in a heart-on-chip featuring oxygen sensing and electrical pacing capabilities
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120495/
https://www.ncbi.nlm.nih.gov/pubmed/35601892
http://dx.doi.org/10.1016/j.mtbio.2022.100280
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