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An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds

The embryonic stem cell test (EST) represents the only validated and accepted in vitro system for the detection and classification of compounds according to their developmental and reproductive teratogenic potency. The widespread implementation of the EST, however, in particular for routine applicat...

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Autores principales: Witt, Gesa, Keminer, Oliver, Leu, Jennifer, Tandon, Rashmi, Meiser, Ina, Willing, Anne, Winschel, Ingo, Abt, Jana-Christin, Brändl, Björn, Sébastien, Isabelle, Friese, Manuel A., Müller, Franz-Josef, Neubauer, Julia C., Claussen, Carsten, Zimmermann, Heiko, Gribbon, Philip, Pless, Ole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012336/
https://www.ncbi.nlm.nih.gov/pubmed/32564278
http://dx.doi.org/10.1007/s10565-020-09538-0
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author Witt, Gesa
Keminer, Oliver
Leu, Jennifer
Tandon, Rashmi
Meiser, Ina
Willing, Anne
Winschel, Ingo
Abt, Jana-Christin
Brändl, Björn
Sébastien, Isabelle
Friese, Manuel A.
Müller, Franz-Josef
Neubauer, Julia C.
Claussen, Carsten
Zimmermann, Heiko
Gribbon, Philip
Pless, Ole
author_facet Witt, Gesa
Keminer, Oliver
Leu, Jennifer
Tandon, Rashmi
Meiser, Ina
Willing, Anne
Winschel, Ingo
Abt, Jana-Christin
Brändl, Björn
Sébastien, Isabelle
Friese, Manuel A.
Müller, Franz-Josef
Neubauer, Julia C.
Claussen, Carsten
Zimmermann, Heiko
Gribbon, Philip
Pless, Ole
author_sort Witt, Gesa
collection PubMed
description The embryonic stem cell test (EST) represents the only validated and accepted in vitro system for the detection and classification of compounds according to their developmental and reproductive teratogenic potency. The widespread implementation of the EST, however, in particular for routine application in pharmaceutical development, has not been achieved so far. Several drawbacks still limit the high-throughput screening of potential drug candidates in this format: The long assay period, the use of non-homogeneous viability assays, the low throughput analysis of marker protein expression and the compatibility of the assay procedures to automation. We have therefore introduced several advancements into the EST workflow: A reduction of the assay period, an introduction of homogeneous viability assays, and a straightforward analysis of marker proteins by flow cytometry and high content imaging to assess the impact of small molecules on differentiation capacity. Most importantly, essential parts of the assay procedure have been adapted to lab automation in 96-well format, thus enabling the interrogation of several compounds in parallel. In addition, extensive investigations were performed to explore the predictive capacity of this next-generation EST, by testing a set of well-known embryotoxicants that encompasses the full range of chemical-inherent embryotoxic potencies possible. Due to these significant improvements, the augmented workflow provides a basis for a sensitive, more rapid, and reproducible high throughput screening compatible platform to predict in vivo developmental toxicity from in vitro data which paves the road towards application in an industrial setting. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10565-020-09538-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-80123362021-04-16 An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds Witt, Gesa Keminer, Oliver Leu, Jennifer Tandon, Rashmi Meiser, Ina Willing, Anne Winschel, Ingo Abt, Jana-Christin Brändl, Björn Sébastien, Isabelle Friese, Manuel A. Müller, Franz-Josef Neubauer, Julia C. Claussen, Carsten Zimmermann, Heiko Gribbon, Philip Pless, Ole Cell Biol Toxicol Original Article The embryonic stem cell test (EST) represents the only validated and accepted in vitro system for the detection and classification of compounds according to their developmental and reproductive teratogenic potency. The widespread implementation of the EST, however, in particular for routine application in pharmaceutical development, has not been achieved so far. Several drawbacks still limit the high-throughput screening of potential drug candidates in this format: The long assay period, the use of non-homogeneous viability assays, the low throughput analysis of marker protein expression and the compatibility of the assay procedures to automation. We have therefore introduced several advancements into the EST workflow: A reduction of the assay period, an introduction of homogeneous viability assays, and a straightforward analysis of marker proteins by flow cytometry and high content imaging to assess the impact of small molecules on differentiation capacity. Most importantly, essential parts of the assay procedure have been adapted to lab automation in 96-well format, thus enabling the interrogation of several compounds in parallel. In addition, extensive investigations were performed to explore the predictive capacity of this next-generation EST, by testing a set of well-known embryotoxicants that encompasses the full range of chemical-inherent embryotoxic potencies possible. Due to these significant improvements, the augmented workflow provides a basis for a sensitive, more rapid, and reproducible high throughput screening compatible platform to predict in vivo developmental toxicity from in vitro data which paves the road towards application in an industrial setting. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10565-020-09538-0) contains supplementary material, which is available to authorized users. Springer Netherlands 2020-06-20 2021 /pmc/articles/PMC8012336/ /pubmed/32564278 http://dx.doi.org/10.1007/s10565-020-09538-0 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Witt, Gesa
Keminer, Oliver
Leu, Jennifer
Tandon, Rashmi
Meiser, Ina
Willing, Anne
Winschel, Ingo
Abt, Jana-Christin
Brändl, Björn
Sébastien, Isabelle
Friese, Manuel A.
Müller, Franz-Josef
Neubauer, Julia C.
Claussen, Carsten
Zimmermann, Heiko
Gribbon, Philip
Pless, Ole
An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds
title An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds
title_full An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds
title_fullStr An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds
title_full_unstemmed An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds
title_short An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds
title_sort automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012336/
https://www.ncbi.nlm.nih.gov/pubmed/32564278
http://dx.doi.org/10.1007/s10565-020-09538-0
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