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Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells

Induced pluripotent stem cells (iPSCs) obtained by reprogramming primary somatic cells have revolutionized the fields of cell biology and disease modeling. However, the number protocols for generating mature muscle fibers with sarcolemmal organization using iPSCs remain limited, and partly mimic the...

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Autores principales: Mazaleyrat, Kilian, Badja, Cherif, Broucqsault, Natacha, Chevalier, Raphaël, Laberthonnière, Camille, Dion, Camille, Baldasseroni, Lyla, El-Yazidi, Claire, Thomas, Morgane, Bachelier, Richard, Altié, Alexandre, Nguyen, Karine, Lévy, Nicolas, Robin, Jérôme D., Magdinier, Frédérique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349825/
https://www.ncbi.nlm.nih.gov/pubmed/32585982
http://dx.doi.org/10.3390/cells9061531
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author Mazaleyrat, Kilian
Badja, Cherif
Broucqsault, Natacha
Chevalier, Raphaël
Laberthonnière, Camille
Dion, Camille
Baldasseroni, Lyla
El-Yazidi, Claire
Thomas, Morgane
Bachelier, Richard
Altié, Alexandre
Nguyen, Karine
Lévy, Nicolas
Robin, Jérôme D.
Magdinier, Frédérique
author_facet Mazaleyrat, Kilian
Badja, Cherif
Broucqsault, Natacha
Chevalier, Raphaël
Laberthonnière, Camille
Dion, Camille
Baldasseroni, Lyla
El-Yazidi, Claire
Thomas, Morgane
Bachelier, Richard
Altié, Alexandre
Nguyen, Karine
Lévy, Nicolas
Robin, Jérôme D.
Magdinier, Frédérique
author_sort Mazaleyrat, Kilian
collection PubMed
description Induced pluripotent stem cells (iPSCs) obtained by reprogramming primary somatic cells have revolutionized the fields of cell biology and disease modeling. However, the number protocols for generating mature muscle fibers with sarcolemmal organization using iPSCs remain limited, and partly mimic the complexity of mature skeletal muscle. Methods: We used a novel combination of small molecules added in a precise sequence for the simultaneous codifferentiation of human iPSCs into skeletal muscle cells and motor neurons. Results: We show that the presence of both cell types reduces the production time for millimeter-long multinucleated muscle fibers with sarcolemmal organization. Muscle fiber contractions are visible in 19–21 days, and can be maintained over long period thanks to the production of innervated multinucleated mature skeletal muscle fibers with autonomous cell regeneration of PAX7-positive cells and extracellular matrix synthesis. The sequential addition of specific molecules recapitulates key steps of human peripheral neurogenesis and myogenesis. Furthermore, this organoid-like culture can be used for functional evaluation and drug screening. Conclusion: Our protocol, which is applicable to hiPSCs from healthy individuals, was validated in Duchenne Muscular Dystrophy, Myotonic Dystrophy, Facio-Scapulo-Humeral Dystrophy and type 2A Limb-Girdle Muscular Dystrophy, opening new paths for the exploration of muscle differentiation, disease modeling and drug discovery.
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spelling pubmed-73498252020-07-15 Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells Mazaleyrat, Kilian Badja, Cherif Broucqsault, Natacha Chevalier, Raphaël Laberthonnière, Camille Dion, Camille Baldasseroni, Lyla El-Yazidi, Claire Thomas, Morgane Bachelier, Richard Altié, Alexandre Nguyen, Karine Lévy, Nicolas Robin, Jérôme D. Magdinier, Frédérique Cells Article Induced pluripotent stem cells (iPSCs) obtained by reprogramming primary somatic cells have revolutionized the fields of cell biology and disease modeling. However, the number protocols for generating mature muscle fibers with sarcolemmal organization using iPSCs remain limited, and partly mimic the complexity of mature skeletal muscle. Methods: We used a novel combination of small molecules added in a precise sequence for the simultaneous codifferentiation of human iPSCs into skeletal muscle cells and motor neurons. Results: We show that the presence of both cell types reduces the production time for millimeter-long multinucleated muscle fibers with sarcolemmal organization. Muscle fiber contractions are visible in 19–21 days, and can be maintained over long period thanks to the production of innervated multinucleated mature skeletal muscle fibers with autonomous cell regeneration of PAX7-positive cells and extracellular matrix synthesis. The sequential addition of specific molecules recapitulates key steps of human peripheral neurogenesis and myogenesis. Furthermore, this organoid-like culture can be used for functional evaluation and drug screening. Conclusion: Our protocol, which is applicable to hiPSCs from healthy individuals, was validated in Duchenne Muscular Dystrophy, Myotonic Dystrophy, Facio-Scapulo-Humeral Dystrophy and type 2A Limb-Girdle Muscular Dystrophy, opening new paths for the exploration of muscle differentiation, disease modeling and drug discovery. MDPI 2020-06-23 /pmc/articles/PMC7349825/ /pubmed/32585982 http://dx.doi.org/10.3390/cells9061531 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mazaleyrat, Kilian
Badja, Cherif
Broucqsault, Natacha
Chevalier, Raphaël
Laberthonnière, Camille
Dion, Camille
Baldasseroni, Lyla
El-Yazidi, Claire
Thomas, Morgane
Bachelier, Richard
Altié, Alexandre
Nguyen, Karine
Lévy, Nicolas
Robin, Jérôme D.
Magdinier, Frédérique
Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells
title Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells
title_full Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells
title_fullStr Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells
title_full_unstemmed Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells
title_short Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells
title_sort multilineage differentiation for formation of innervated skeletal muscle fibers from healthy and diseased human pluripotent stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349825/
https://www.ncbi.nlm.nih.gov/pubmed/32585982
http://dx.doi.org/10.3390/cells9061531
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