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Creating tissue on chip constructs in microtitre plates for drug discovery

We report upon a novel coplanar dielectrophoresis (DEP) based cell patterning system for generating transferrable hepatic cell constructs, resembling a liver-lobule, in culture. The use of paper reinforced gel substrates provided sufficient strength to enable these constructs to be transfered into 9...

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Detalles Bibliográficos
Autores principales: Macdonald, N. P., Menachery, A., Reboud, J., Cooper, J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078682/
https://www.ncbi.nlm.nih.gov/pubmed/35540822
http://dx.doi.org/10.1039/c8ra00849c
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author Macdonald, N. P.
Menachery, A.
Reboud, J.
Cooper, J. M.
author_facet Macdonald, N. P.
Menachery, A.
Reboud, J.
Cooper, J. M.
author_sort Macdonald, N. P.
collection PubMed
description We report upon a novel coplanar dielectrophoresis (DEP) based cell patterning system for generating transferrable hepatic cell constructs, resembling a liver-lobule, in culture. The use of paper reinforced gel substrates provided sufficient strength to enable these constructs to be transfered into 96-well plates for long term functional studies, including in the future, drug development studies. Experimental results showed that hepatic cells formed DEP field-induced structures corresponding to an array of lobule-mimetic patterns. Hepatic viability was observed over a period of 3 days by the use of a fluorescent cell staining technique, whilst the liver specific functionality of albumin secretion showed a significant enhancement due to the layer patterning of cell lines (HepG2/C3A), compared to 2D patterned cells and un-patterned control. This “build and transfer” concept could, in future, also be adapted for the layer-by-layer construction of organs-on-chip in microtitre formats.
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spelling pubmed-90786822022-05-09 Creating tissue on chip constructs in microtitre plates for drug discovery Macdonald, N. P. Menachery, A. Reboud, J. Cooper, J. M. RSC Adv Chemistry We report upon a novel coplanar dielectrophoresis (DEP) based cell patterning system for generating transferrable hepatic cell constructs, resembling a liver-lobule, in culture. The use of paper reinforced gel substrates provided sufficient strength to enable these constructs to be transfered into 96-well plates for long term functional studies, including in the future, drug development studies. Experimental results showed that hepatic cells formed DEP field-induced structures corresponding to an array of lobule-mimetic patterns. Hepatic viability was observed over a period of 3 days by the use of a fluorescent cell staining technique, whilst the liver specific functionality of albumin secretion showed a significant enhancement due to the layer patterning of cell lines (HepG2/C3A), compared to 2D patterned cells and un-patterned control. This “build and transfer” concept could, in future, also be adapted for the layer-by-layer construction of organs-on-chip in microtitre formats. The Royal Society of Chemistry 2018-03-06 /pmc/articles/PMC9078682/ /pubmed/35540822 http://dx.doi.org/10.1039/c8ra00849c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Macdonald, N. P.
Menachery, A.
Reboud, J.
Cooper, J. M.
Creating tissue on chip constructs in microtitre plates for drug discovery
title Creating tissue on chip constructs in microtitre plates for drug discovery
title_full Creating tissue on chip constructs in microtitre plates for drug discovery
title_fullStr Creating tissue on chip constructs in microtitre plates for drug discovery
title_full_unstemmed Creating tissue on chip constructs in microtitre plates for drug discovery
title_short Creating tissue on chip constructs in microtitre plates for drug discovery
title_sort creating tissue on chip constructs in microtitre plates for drug discovery
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078682/
https://www.ncbi.nlm.nih.gov/pubmed/35540822
http://dx.doi.org/10.1039/c8ra00849c
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