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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
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.
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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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