Abstract
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 muscles7.
Original language | English |
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Article number | e51243 |
Journal | Journal of visualized experiments : JoVE |
Issue number | 88 |
DOIs | |
Publication status | Published - Jun 21 2014 |
Keywords
- Bioengineering
- Cells
- Chromatin
- Embryonic Structures
- Epinegetics
- hESC
- Infection
- Issue 88
- Lentivirus
- Musculoskeletal Diseases
- Musculoskeletal System
- Myosphere
- Skeletal Myogenesis
- Tissues
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Chemical Engineering(all)
- Immunology and Microbiology(all)
- Neuroscience(all)
- Medicine(all)