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Modeling and Targeting Neuroglial Interactions with Human Pluripotent Stem Cell Models

Generation of relevant and robust models for neurological disorders is of main importance for both target identification and drug discovery. The non-cell autonomous effects of glial cells on neurons have been described in a broad range of neurodegenerative and neurodevelopmental disorders, pointing...

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Autores principales: Bigarreau, Julie, Rouach, Nathalie, Perrier, Anselme L., Mouthon, Franck, Charvériat, Mathieu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836094/
https://www.ncbi.nlm.nih.gov/pubmed/35163606
http://dx.doi.org/10.3390/ijms23031684
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author Bigarreau, Julie
Rouach, Nathalie
Perrier, Anselme L.
Mouthon, Franck
Charvériat, Mathieu
author_facet Bigarreau, Julie
Rouach, Nathalie
Perrier, Anselme L.
Mouthon, Franck
Charvériat, Mathieu
author_sort Bigarreau, Julie
collection PubMed
description Generation of relevant and robust models for neurological disorders is of main importance for both target identification and drug discovery. The non-cell autonomous effects of glial cells on neurons have been described in a broad range of neurodegenerative and neurodevelopmental disorders, pointing to neuroglial interactions as novel alternative targets for therapeutics development. Interestingly, the recent breakthrough discovery of human induced pluripotent stem cells (hiPSCs) has opened a new road for studying neurological and neurodevelopmental disorders “in a dish”. Here, we provide an overview of the generation and modeling of both neuronal and glial cells from human iPSCs and a brief synthesis of recent work investigating neuroglial interactions using hiPSCs in a pathophysiological context.
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spelling pubmed-88360942022-02-12 Modeling and Targeting Neuroglial Interactions with Human Pluripotent Stem Cell Models Bigarreau, Julie Rouach, Nathalie Perrier, Anselme L. Mouthon, Franck Charvériat, Mathieu Int J Mol Sci Review Generation of relevant and robust models for neurological disorders is of main importance for both target identification and drug discovery. The non-cell autonomous effects of glial cells on neurons have been described in a broad range of neurodegenerative and neurodevelopmental disorders, pointing to neuroglial interactions as novel alternative targets for therapeutics development. Interestingly, the recent breakthrough discovery of human induced pluripotent stem cells (hiPSCs) has opened a new road for studying neurological and neurodevelopmental disorders “in a dish”. Here, we provide an overview of the generation and modeling of both neuronal and glial cells from human iPSCs and a brief synthesis of recent work investigating neuroglial interactions using hiPSCs in a pathophysiological context. MDPI 2022-01-31 /pmc/articles/PMC8836094/ /pubmed/35163606 http://dx.doi.org/10.3390/ijms23031684 Text en © 2022 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
Bigarreau, Julie
Rouach, Nathalie
Perrier, Anselme L.
Mouthon, Franck
Charvériat, Mathieu
Modeling and Targeting Neuroglial Interactions with Human Pluripotent Stem Cell Models
title Modeling and Targeting Neuroglial Interactions with Human Pluripotent Stem Cell Models
title_full Modeling and Targeting Neuroglial Interactions with Human Pluripotent Stem Cell Models
title_fullStr Modeling and Targeting Neuroglial Interactions with Human Pluripotent Stem Cell Models
title_full_unstemmed Modeling and Targeting Neuroglial Interactions with Human Pluripotent Stem Cell Models
title_short Modeling and Targeting Neuroglial Interactions with Human Pluripotent Stem Cell Models
title_sort modeling and targeting neuroglial interactions with human pluripotent stem cell models
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836094/
https://www.ncbi.nlm.nih.gov/pubmed/35163606
http://dx.doi.org/10.3390/ijms23031684
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