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Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders
One of the major obstacles to the identification of therapeutic interventions for central nervous system disorders has been the difficulty in studying the step-by-step progression of diseases in neuronal networks that are amenable to drug screening. Recent advances in the field of human pluripotent...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699352/ https://www.ncbi.nlm.nih.gov/pubmed/34943799 http://dx.doi.org/10.3390/cells10123290 |
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author | Benchoua, Alexandra Lasbareilles, Marie Tournois, Johana |
author_facet | Benchoua, Alexandra Lasbareilles, Marie Tournois, Johana |
author_sort | Benchoua, Alexandra |
collection | PubMed |
description | One of the major obstacles to the identification of therapeutic interventions for central nervous system disorders has been the difficulty in studying the step-by-step progression of diseases in neuronal networks that are amenable to drug screening. Recent advances in the field of human pluripotent stem cell (PSC) biology offers the capability to create patient-specific human neurons with defined clinical profiles using reprogramming technology, which provides unprecedented opportunities for both the investigation of pathogenic mechanisms of brain disorders and the discovery of novel therapeutic strategies via drug screening. Many examples not only of the creation of human pluripotent stem cells as models of monogenic neurological disorders, but also of more challenging cases of complex multifactorial disorders now exist. Here, we review the state-of-the art brain cell types obtainable from PSCs and amenable to compound-screening formats. We then provide examples illustrating how these models contribute to the definition of new molecular or functional targets for drug discovery and to the design of novel pharmacological approaches for rare genetic disorders, as well as frequent neurodegenerative diseases and psychiatric disorders. |
format | Online Article Text |
id | pubmed-8699352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86993522021-12-24 Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders Benchoua, Alexandra Lasbareilles, Marie Tournois, Johana Cells Review One of the major obstacles to the identification of therapeutic interventions for central nervous system disorders has been the difficulty in studying the step-by-step progression of diseases in neuronal networks that are amenable to drug screening. Recent advances in the field of human pluripotent stem cell (PSC) biology offers the capability to create patient-specific human neurons with defined clinical profiles using reprogramming technology, which provides unprecedented opportunities for both the investigation of pathogenic mechanisms of brain disorders and the discovery of novel therapeutic strategies via drug screening. Many examples not only of the creation of human pluripotent stem cells as models of monogenic neurological disorders, but also of more challenging cases of complex multifactorial disorders now exist. Here, we review the state-of-the art brain cell types obtainable from PSCs and amenable to compound-screening formats. We then provide examples illustrating how these models contribute to the definition of new molecular or functional targets for drug discovery and to the design of novel pharmacological approaches for rare genetic disorders, as well as frequent neurodegenerative diseases and psychiatric disorders. MDPI 2021-11-24 /pmc/articles/PMC8699352/ /pubmed/34943799 http://dx.doi.org/10.3390/cells10123290 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Benchoua, Alexandra Lasbareilles, Marie Tournois, Johana Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders |
title | Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders |
title_full | Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders |
title_fullStr | Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders |
title_full_unstemmed | Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders |
title_short | Contribution of Human Pluripotent Stem Cell-Based Models to Drug Discovery for Neurological Disorders |
title_sort | contribution of human pluripotent stem cell-based models to drug discovery for neurological disorders |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699352/ https://www.ncbi.nlm.nih.gov/pubmed/34943799 http://dx.doi.org/10.3390/cells10123290 |
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