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Generation of Myospheres From hESCs by Epigenetic Reprogramming

Generation of a homogeneous and abundant population of skeletal muscle cells from human embryonic stem cells (hESCs) is a requirement for cell-based therapies and for a "disease in a dish" model of human neuromuscular diseases. Major hurdles, such as low abundance and heterogeneity of the...

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Detalles Bibliográficos
Autores principales: Albini, Sonia, Puri, Pier Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203277/
https://www.ncbi.nlm.nih.gov/pubmed/24999032
http://dx.doi.org/10.3791/51243
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author Albini, Sonia
Puri, Pier Lorenzo
author_facet Albini, Sonia
Puri, Pier Lorenzo
author_sort Albini, Sonia
collection PubMed
description Generation of a homogeneous and abundant population of skeletal muscle cells from human embryonic stem cells (hESCs) is a requirement for cell-based therapies and for a "disease in a dish" model of human neuromuscular diseases. Major hurdles, such as low abundance and heterogeneity of the population of interest, as well as a lack of protocols for the formation of three-dimensional contractile structures, have limited the applications of stem cells for neuromuscular disorders. We have designed a protocol that overcomes these limits by ectopic introduction of defined factors in hESCs - the muscle determination factor MyoD and SWI/SNF chromatin remodeling complex component BAF60C - that are able to reprogram hESCs into skeletal muscle cells. Here we describe the protocol established to generate hESC-derived myoblasts and promote their clustering into tridimensional miniaturized structures (myospheres) that functionally mimic miniaturized skeletal muscles(7).
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spelling pubmed-42032772014-10-22 Generation of Myospheres From hESCs by Epigenetic Reprogramming Albini, Sonia Puri, Pier Lorenzo J Vis Exp Bioengineering Generation of a homogeneous and abundant population of skeletal muscle cells from human embryonic stem cells (hESCs) is a requirement for cell-based therapies and for a "disease in a dish" model of human neuromuscular diseases. Major hurdles, such as low abundance and heterogeneity of the population of interest, as well as a lack of protocols for the formation of three-dimensional contractile structures, have limited the applications of stem cells for neuromuscular disorders. We have designed a protocol that overcomes these limits by ectopic introduction of defined factors in hESCs - the muscle determination factor MyoD and SWI/SNF chromatin remodeling complex component BAF60C - that are able to reprogram hESCs into skeletal muscle cells. Here we describe the protocol established to generate hESC-derived myoblasts and promote their clustering into tridimensional miniaturized structures (myospheres) that functionally mimic miniaturized skeletal muscles(7). MyJove Corporation 2014-06-21 /pmc/articles/PMC4203277/ /pubmed/24999032 http://dx.doi.org/10.3791/51243 Text en Copyright © 2014, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Bioengineering
Albini, Sonia
Puri, Pier Lorenzo
Generation of Myospheres From hESCs by Epigenetic Reprogramming
title Generation of Myospheres From hESCs by Epigenetic Reprogramming
title_full Generation of Myospheres From hESCs by Epigenetic Reprogramming
title_fullStr Generation of Myospheres From hESCs by Epigenetic Reprogramming
title_full_unstemmed Generation of Myospheres From hESCs by Epigenetic Reprogramming
title_short Generation of Myospheres From hESCs by Epigenetic Reprogramming
title_sort generation of myospheres from hescs by epigenetic reprogramming
topic Bioengineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203277/
https://www.ncbi.nlm.nih.gov/pubmed/24999032
http://dx.doi.org/10.3791/51243
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