ArticleThe Journal of physiology1991
Comparison of initial stages of muscle differentiation in rat and mouse myoblastic and mouse mesodermal stem cell lines.
Article in The Journal of physiology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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Who cites it
20 citing papers in PubMed, 69 citations in OpenAlex.
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- Effects of miR-34c-5p on Sodium, Potassium, and Calcium Channel Currents in C2C12 Myotubes.Cellular and molecular neurobiology · 2020Article
- Bioelectric Properties of Myogenic Progenitor Cells.Bioelectricity · 2019Review
- Cancer affects microRNA expression, release, and function in cardiac and skeletal muscle.Cancer research · 2014Article
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- Transcriptional profile of GTP-mediated differentiation of C2C12 skeletal muscle cells.Purinergic signalling · 2012Article
- Sodium arsenite represses the expression of myogenin in C2C12 mouse myoblast cells through histone modifications and altered expression of Ezh2, Glp, and Igf-1.Toxicology and applied pharmacology · 2012Article
- Recombinant adenoviral microRNA-206 induces myogenesis in C2C12 cells.Medical science monitor : international medical journal of experimental and clinical research · 2011Article
- Sodium arsenite delays the differentiation of C2C12 mouse myoblast cells and alters methylation patterns on the transcription factor myogenin.Toxicology and applied pharmacology · 2011Article
- Autoregulation of Fox protein expression to produce dominant negative splicing factors.RNA (New York, N.Y.) · 2010Article
- Role of membrane potential in the regulation of cell proliferation and differentiation.Stem cell reviews and reports · 2009Review
- Secretion of adenylate kinase 1 is required for extracellular ATP synthesis in C2C12 myotubes.Experimental & molecular medicine · 2008Article
- Neural cell adhesion molecule (NCAM) marks adult myogenic cells committed to differentiation.Experimental cell research · 2008Article
- Hypercholesterolemia suppresses Kir channels in porcine bone marrow progenitor cells in vivo.Biochemical and biophysical research communications · 2007Article
- Extracellular guanosine-5'-triphosphate modulates myogenesis via intermediate Ca(2+)-activated K+ currents in C2C12 mouse cells.The Journal of physiology · 2006Article
- Homologues of the Caenorhabditis elegans Fox-1 protein are neuronal splicing regulators in mammals.Molecular and cellular biology · 2005Article
- Expression of ion channels during differentiation of a human skeletal muscle cell line.Journal of muscle research and cell motility · 1997Article
- Properties of ionic currents induced by external ATP in a mouse mesodermal stem cell line.The Journal of physiology · 1991Article
- Electrophysiological and immunohistochemical analysis of muscle differentiation in a mouse mesodermal stem cell line.The Journal of physiology · 1991Article
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Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
1. Electrophysiological and immunohistochemical properties during the early stages of muscle differentiation were studied in two myoblastic cell lines, mouse C2C12 and rat L6, and compared to those in myogenic clonal cells derived from the mouse mesodermal stem cell line C3H10T1/2, studied in the preceding paper. 2. Mouse C2C12 cells were induced to differentiate to muscle by changing from 10% fetal calf serum to 2% horse serum in the medium. Most of the C2C12 cells before serum reduction showed ATP-induced slow K+ current. Twelve per cent showed inward rectifier K+ current. They expressed fibronectin and Neural Cell Adhesion Molecule (NCAM). Small spindle-shaped cells at an early stage of muscle differentiation began to appear 24 h after serum reduction. In contrast to cells before serum reduction, only 13% of these spindle-shaped cells showed an ATP response. Most showed tetrodotoxin (TTX)-resistant Na+ current and outward K+ current. Thirty-eight per cent had inward rectifier K+ current. They expressed NCAM but not fibronectin. The T-type Ca2+ current was not observed up to the latest stage of differentiation investigated. 3. Rat L6 cells in maintaining culture medium showed only infrequent ATP responses, but already showed TTX-resistant Na+ current. No clear T-type Ca2+, inward rectifier K+ or outward K+ currents were observed. About one-third of the cells did not express fibronectin. From these results, L6 cells appear to be at a stage near to but slightly earlier than that of C2C12 cells after serum reduction. 4. The properties of the early stages of muscle differentiation in C3H10T1/2 cells, such as the disappearance of ATP-induced K+ current and fibronectin, and the appearance of NCAM, were also seen in C2C12 and L6. However, T-type Ca2+ and inward K+ currents, which were found in the initial stages of C3H10T1/2 muscle differentiation, were not clearly observed in C2C12 and L6. Instead, C2C12 and L6 showed a TTX-resistant Na+ current which was never observed in C3H10T1/2 cells. 5. The properties of the TTX-resistant Na+ current were investigated. In L6 cells, it was reduced to 60% by 1 microM-TTX. It could be evoked by depolarizations to a level above -50 mV with a maximum amplitude at around -15 mV. Steady-state inactivation was detectable with pre-pulses to -100 mV for 100 ms and reached half at pre-pulses of -78 mV. These parameters of inactivation are clearly different from those of the TTX-sensitive Na+ current observed in C3H10T1/2-derived mature muscle cells in the preceding paper.
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