Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1994-8-11
pubmed:abstractText
The mouse blastocyst-derived embryonic stem cell (ES cell) line BLC6 efficiently differentiates into myosin heavy chain-, desmin- and myogenin-positive skeletal muscle cells when cultivated in embryo-like aggregates (embryoid bodies). Here, we show that the muscle-specific determination genes myf5, myogenin, myoD, and myf6 are expressed in these embryoid bodies in a characteristic temporal pattern which precisely reflects the sequence observed during mouse development in vivo. Myf5 is the first gene to be expressed followed by myogenin, myoD, and myf6, in this order. In situ hybridization demonstrates transcripts for myogenin and myoD accumulating in mono- and multinucleated myogenic cells, while myf5 mRNA is already found in mononucleated myoblasts. The myocytes also express functional nicotinic cholinoceptors and exhibit T-type Ca2+ currents and later L-type Ca2+ currents, demonstrating physiological properties of skeletal muscle cells. During myocyte differentiation the density of L-type Ca2+ channels significantly increases while the density of T-type Ca2+ channels decreases. The effect of external signals on myogenic differentiation of BLC6 cells was demonstrated by cocultivation with visceral endodermal END-2 cells and the activin A-secreting WEHI-3 cells. END-2 cells essentially prevent skeletal muscle differentiation, whereas basic fibroblast growth factor, transforming growth factor-beta, and WEHI-3 cells have no or an attenuating effect, respectively. Our results suggest that ES cells recapitulate closely the early steps of muscle development in vivo and may serve as an excellent in vitro system to study this process.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Epidermal Growth Factor, http://linkedlifedata.com/resource/pubmed/chemical/Muscle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Myf5 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/MyoD Protein, http://linkedlifedata.com/resource/pubmed/chemical/Myog protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Myogenic Regulatory Factor 5, http://linkedlifedata.com/resource/pubmed/chemical/Myogenic Regulatory Factors, http://linkedlifedata.com/resource/pubmed/chemical/Myogenin, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Nicotinic, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/myogenic factor 6
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0012-1606
pubmed:author
pubmed:issnType
Print
pubmed:volume
164
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
87-101
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:8026639-Animals, pubmed-meshheading:8026639-Calcium Channels, pubmed-meshheading:8026639-Cell Differentiation, pubmed-meshheading:8026639-Cells, Cultured, pubmed-meshheading:8026639-DNA-Binding Proteins, pubmed-meshheading:8026639-Embryo, Mammalian, pubmed-meshheading:8026639-Epidermal Growth Factor, pubmed-meshheading:8026639-Gene Expression Regulation, pubmed-meshheading:8026639-Genes, Regulator, pubmed-meshheading:8026639-Mice, pubmed-meshheading:8026639-Muscle Proteins, pubmed-meshheading:8026639-Muscles, pubmed-meshheading:8026639-MyoD Protein, pubmed-meshheading:8026639-Myogenic Regulatory Factor 5, pubmed-meshheading:8026639-Myogenic Regulatory Factors, pubmed-meshheading:8026639-Myogenin, pubmed-meshheading:8026639-Receptors, Nicotinic, pubmed-meshheading:8026639-Stem Cells, pubmed-meshheading:8026639-Trans-Activators
pubmed:year
1994
pubmed:articleTitle
Muscle cell differentiation of embryonic stem cells reflects myogenesis in vivo: developmentally regulated expression of myogenic determination genes and functional expression of ionic currents.
pubmed:affiliation
Institute of Plant Genetics and Crop Plant Research, Gatersleben, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't