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A multiparametric activity profiling platform for neuron disease phenotyping and drug screening
Patient stem cell–derived models enable imaging of complex disease phenotypes and the development of scalable drug discovery platforms. Current preclinical methods for assessing cellular activity do not, however, capture the full intricacies of disease-induced disturbances and instead typically focu...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9265164/ https://www.ncbi.nlm.nih.gov/pubmed/34910584 http://dx.doi.org/10.1091/mbc.E21-10-0481 |
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author | Boivin, Bruno Roet, Kasper C. D. Huang, Xuan Karhohs, Kyle W. Rohban, Mohammad H. Sandoe, Jack Wiskow, Ole Maeda, Rie Grantham, Alyssa Dornon, Mary K. Shao, Jenny Frost, Devlin Baker, Dylan Eggan, Kevin Carpenter, Anne E. Woolf, Clifford J. |
author_facet | Boivin, Bruno Roet, Kasper C. D. Huang, Xuan Karhohs, Kyle W. Rohban, Mohammad H. Sandoe, Jack Wiskow, Ole Maeda, Rie Grantham, Alyssa Dornon, Mary K. Shao, Jenny Frost, Devlin Baker, Dylan Eggan, Kevin Carpenter, Anne E. Woolf, Clifford J. |
author_sort | Boivin, Bruno |
collection | PubMed |
description | Patient stem cell–derived models enable imaging of complex disease phenotypes and the development of scalable drug discovery platforms. Current preclinical methods for assessing cellular activity do not, however, capture the full intricacies of disease-induced disturbances and instead typically focus on a single parameter, which impairs both the understanding of disease and the discovery of effective therapeutics. Here, we describe a cloud-based image processing and analysis platform that captures the intricate activity profile revealed by GCaMP fluorescence recordings of intracellular calcium changes and enables the discovery of molecules that correct 153 parameters that define the amyotrophic lateral sclerosis motor neuron disease phenotype. In a high-throughput screen, we identified compounds that revert the multiparametric disease profile to that found in healthy cells, a novel and robust measure of therapeutic potential quite distinct from unidimensional screening. This platform can guide the development of therapeutics that counteract the multifaceted pathological features of diseased cellular activity. |
format | Online Article Text |
id | pubmed-9265164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92651642022-07-27 A multiparametric activity profiling platform for neuron disease phenotyping and drug screening Boivin, Bruno Roet, Kasper C. D. Huang, Xuan Karhohs, Kyle W. Rohban, Mohammad H. Sandoe, Jack Wiskow, Ole Maeda, Rie Grantham, Alyssa Dornon, Mary K. Shao, Jenny Frost, Devlin Baker, Dylan Eggan, Kevin Carpenter, Anne E. Woolf, Clifford J. Mol Biol Cell Articles Patient stem cell–derived models enable imaging of complex disease phenotypes and the development of scalable drug discovery platforms. Current preclinical methods for assessing cellular activity do not, however, capture the full intricacies of disease-induced disturbances and instead typically focus on a single parameter, which impairs both the understanding of disease and the discovery of effective therapeutics. Here, we describe a cloud-based image processing and analysis platform that captures the intricate activity profile revealed by GCaMP fluorescence recordings of intracellular calcium changes and enables the discovery of molecules that correct 153 parameters that define the amyotrophic lateral sclerosis motor neuron disease phenotype. In a high-throughput screen, we identified compounds that revert the multiparametric disease profile to that found in healthy cells, a novel and robust measure of therapeutic potential quite distinct from unidimensional screening. This platform can guide the development of therapeutics that counteract the multifaceted pathological features of diseased cellular activity. The American Society for Cell Biology 2022-05-12 /pmc/articles/PMC9265164/ /pubmed/34910584 http://dx.doi.org/10.1091/mbc.E21-10-0481 Text en © 2022 Boivin, Roet, et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License. |
spellingShingle | Articles Boivin, Bruno Roet, Kasper C. D. Huang, Xuan Karhohs, Kyle W. Rohban, Mohammad H. Sandoe, Jack Wiskow, Ole Maeda, Rie Grantham, Alyssa Dornon, Mary K. Shao, Jenny Frost, Devlin Baker, Dylan Eggan, Kevin Carpenter, Anne E. Woolf, Clifford J. A multiparametric activity profiling platform for neuron disease phenotyping and drug screening |
title | A multiparametric activity profiling platform for neuron disease phenotyping and drug screening |
title_full | A multiparametric activity profiling platform for neuron disease phenotyping and drug screening |
title_fullStr | A multiparametric activity profiling platform for neuron disease phenotyping and drug screening |
title_full_unstemmed | A multiparametric activity profiling platform for neuron disease phenotyping and drug screening |
title_short | A multiparametric activity profiling platform for neuron disease phenotyping and drug screening |
title_sort | multiparametric activity profiling platform for neuron disease phenotyping and drug screening |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9265164/ https://www.ncbi.nlm.nih.gov/pubmed/34910584 http://dx.doi.org/10.1091/mbc.E21-10-0481 |
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