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Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening
Patient-derived cellular models become an increasingly powerful tool to model human diseases for precision medicine approaches. The identification of robust cellular disease phenotypes in these models paved the way towards high throughput screenings (HTS) including the implementation of laboratory a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809482/ https://www.ncbi.nlm.nih.gov/pubmed/33446877 http://dx.doi.org/10.1038/s41598-021-81129-3 |
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author | Boussaad, Ibrahim Cruciani, Gérald Bolognin, Silvia Antony, Paul Dording, Claire M. Kwon, Yong-Jun Heutink, Peter Fava, Eugenio Schwamborn, Jens C. Krüger, Rejko |
author_facet | Boussaad, Ibrahim Cruciani, Gérald Bolognin, Silvia Antony, Paul Dording, Claire M. Kwon, Yong-Jun Heutink, Peter Fava, Eugenio Schwamborn, Jens C. Krüger, Rejko |
author_sort | Boussaad, Ibrahim |
collection | PubMed |
description | Patient-derived cellular models become an increasingly powerful tool to model human diseases for precision medicine approaches. The identification of robust cellular disease phenotypes in these models paved the way towards high throughput screenings (HTS) including the implementation of laboratory advanced automation. However, maintenance and expansion of cells for HTS remains largely manual work. Here, we describe an integrated, complex automated platform for HTS in a translational research setting also designed for maintenance and expansion of different cell types. The comprehensive design allows automation of all cultivation steps and is flexible for development of methods for variable cell types. We demonstrate protocols for controlled cell seeding, splitting and expansion of human fibroblasts, induced pluripotent stem cells (iPSC), and neural progenitor cells (NPC) that allow for subsequent differentiation into different cell types and image-based multiparametric screening. Furthermore, we provide automated protocols for neuronal differentiation of NPC in 2D culture and 3D midbrain organoids for HTS. The flexibility of this multitask platform makes it an ideal solution for translational research settings involving experiments on different patient-derived cellular models for precision medicine. |
format | Online Article Text |
id | pubmed-7809482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78094822021-01-21 Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening Boussaad, Ibrahim Cruciani, Gérald Bolognin, Silvia Antony, Paul Dording, Claire M. Kwon, Yong-Jun Heutink, Peter Fava, Eugenio Schwamborn, Jens C. Krüger, Rejko Sci Rep Article Patient-derived cellular models become an increasingly powerful tool to model human diseases for precision medicine approaches. The identification of robust cellular disease phenotypes in these models paved the way towards high throughput screenings (HTS) including the implementation of laboratory advanced automation. However, maintenance and expansion of cells for HTS remains largely manual work. Here, we describe an integrated, complex automated platform for HTS in a translational research setting also designed for maintenance and expansion of different cell types. The comprehensive design allows automation of all cultivation steps and is flexible for development of methods for variable cell types. We demonstrate protocols for controlled cell seeding, splitting and expansion of human fibroblasts, induced pluripotent stem cells (iPSC), and neural progenitor cells (NPC) that allow for subsequent differentiation into different cell types and image-based multiparametric screening. Furthermore, we provide automated protocols for neuronal differentiation of NPC in 2D culture and 3D midbrain organoids for HTS. The flexibility of this multitask platform makes it an ideal solution for translational research settings involving experiments on different patient-derived cellular models for precision medicine. Nature Publishing Group UK 2021-01-14 /pmc/articles/PMC7809482/ /pubmed/33446877 http://dx.doi.org/10.1038/s41598-021-81129-3 Text en © The Author(s) 2021 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 | Article Boussaad, Ibrahim Cruciani, Gérald Bolognin, Silvia Antony, Paul Dording, Claire M. Kwon, Yong-Jun Heutink, Peter Fava, Eugenio Schwamborn, Jens C. Krüger, Rejko Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening |
title | Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening |
title_full | Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening |
title_fullStr | Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening |
title_full_unstemmed | Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening |
title_short | Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening |
title_sort | integrated, automated maintenance, expansion and differentiation of 2d and 3d patient-derived cellular models for high throughput drug screening |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809482/ https://www.ncbi.nlm.nih.gov/pubmed/33446877 http://dx.doi.org/10.1038/s41598-021-81129-3 |
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