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3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing
Parkinson's disease (PD)‐specific neurons, grown in standard 2D cultures, typically only display weak endophenotypes. The cultivation of PD patient‐specific neurons, derived from induced pluripotent stem cells carrying the LRRK2‐G2019S mutation, is optimized in 3D microfluidics. The automated i...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325628/ https://www.ncbi.nlm.nih.gov/pubmed/30643711 http://dx.doi.org/10.1002/advs.201800927 |
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author | Bolognin, Silvia Fossépré, Marie Qing, Xiaobing Jarazo, Javier Ščančar, Janez Moreno, Edinson Lucumi Nickels, Sarah L. Wasner, Kobi Ouzren, Nassima Walter, Jonas Grünewald, Anne Glaab, Enrico Salamanca, Luis Fleming, Ronan M. T. Antony, Paul M. A. Schwamborn, Jens C. |
author_facet | Bolognin, Silvia Fossépré, Marie Qing, Xiaobing Jarazo, Javier Ščančar, Janez Moreno, Edinson Lucumi Nickels, Sarah L. Wasner, Kobi Ouzren, Nassima Walter, Jonas Grünewald, Anne Glaab, Enrico Salamanca, Luis Fleming, Ronan M. T. Antony, Paul M. A. Schwamborn, Jens C. |
author_sort | Bolognin, Silvia |
collection | PubMed |
description | Parkinson's disease (PD)‐specific neurons, grown in standard 2D cultures, typically only display weak endophenotypes. The cultivation of PD patient‐specific neurons, derived from induced pluripotent stem cells carrying the LRRK2‐G2019S mutation, is optimized in 3D microfluidics. The automated image analysis algorithms are implemented to enable pharmacophenomics in disease‐relevant conditions. In contrast to 2D cultures, this 3D approach reveals robust endophenotypes. High‐content imaging data show decreased dopaminergic differentiation and branching complexity, altered mitochondrial morphology, and increased cell death in LRRK2‐G2019S neurons compared to isogenic lines without using stressor agents. Treatment with the LRRK2 inhibitor 2 (Inh2) rescues LRRK2‐G2019S‐dependent dopaminergic phenotypes. Strikingly, a holistic analysis of all studied features shows that the genetic background of the PD patients, and not the LRRK2‐G2019S mutation, constitutes the strongest contribution to the phenotypes. These data support the use of advanced in vitro models for future patient stratification and personalized drug development. |
format | Online Article Text |
id | pubmed-6325628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63256282019-01-14 3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing Bolognin, Silvia Fossépré, Marie Qing, Xiaobing Jarazo, Javier Ščančar, Janez Moreno, Edinson Lucumi Nickels, Sarah L. Wasner, Kobi Ouzren, Nassima Walter, Jonas Grünewald, Anne Glaab, Enrico Salamanca, Luis Fleming, Ronan M. T. Antony, Paul M. A. Schwamborn, Jens C. Adv Sci (Weinh) Full Papers Parkinson's disease (PD)‐specific neurons, grown in standard 2D cultures, typically only display weak endophenotypes. The cultivation of PD patient‐specific neurons, derived from induced pluripotent stem cells carrying the LRRK2‐G2019S mutation, is optimized in 3D microfluidics. The automated image analysis algorithms are implemented to enable pharmacophenomics in disease‐relevant conditions. In contrast to 2D cultures, this 3D approach reveals robust endophenotypes. High‐content imaging data show decreased dopaminergic differentiation and branching complexity, altered mitochondrial morphology, and increased cell death in LRRK2‐G2019S neurons compared to isogenic lines without using stressor agents. Treatment with the LRRK2 inhibitor 2 (Inh2) rescues LRRK2‐G2019S‐dependent dopaminergic phenotypes. Strikingly, a holistic analysis of all studied features shows that the genetic background of the PD patients, and not the LRRK2‐G2019S mutation, constitutes the strongest contribution to the phenotypes. These data support the use of advanced in vitro models for future patient stratification and personalized drug development. John Wiley and Sons Inc. 2018-11-20 /pmc/articles/PMC6325628/ /pubmed/30643711 http://dx.doi.org/10.1002/advs.201800927 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Bolognin, Silvia Fossépré, Marie Qing, Xiaobing Jarazo, Javier Ščančar, Janez Moreno, Edinson Lucumi Nickels, Sarah L. Wasner, Kobi Ouzren, Nassima Walter, Jonas Grünewald, Anne Glaab, Enrico Salamanca, Luis Fleming, Ronan M. T. Antony, Paul M. A. Schwamborn, Jens C. 3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing |
title | 3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing |
title_full | 3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing |
title_fullStr | 3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing |
title_full_unstemmed | 3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing |
title_short | 3D Cultures of Parkinson's Disease‐Specific Dopaminergic Neurons for High Content Phenotyping and Drug Testing |
title_sort | 3d cultures of parkinson's disease‐specific dopaminergic neurons for high content phenotyping and drug testing |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325628/ https://www.ncbi.nlm.nih.gov/pubmed/30643711 http://dx.doi.org/10.1002/advs.201800927 |
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