Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1973 Mar;229(3):751–766.2. doi: 10.1113/jphysiol.1973.sp010165

A physiological study of chick myotubes grown in tissue culture

J B Harris, M W Marshall, P Wilson
PMCID: PMC1350561  PMID: 4735059

Abstract

1. A study has been made of some passive and active membrane properties of myotubes of different ages obtained in culture from explants of chick embryo thigh muscle.

2. After 3 days in vitro the mean values for the myotube resting membrane potential and input resistance were - 63·8 mV and 1·30 MΩ respectively. By 13 days these values had fallen to - 51·0 mV and 0·80 MΩ.

3. Current/voltage relations were measured in the presence of tetrodotoxin. The relations were linear for membrane potentials between - 120 and - 35 mV. Further depolarization usually resulted in a delayed increase in conductance which inactivated with time.

4. All myotubes tested using anodal break excitation were capable of generating action potentials. Action potentials were blocked by tetrodotoxin, saxitoxin and procaine.

5. All myotubes were sensitive to iontophoretically applied ACh. The potential change produced by ACh reversed polarity at a membrane potential between 0 and + 10 mV. The depolarization produced by ACh was unaffected by anticholinesterases.

6. The ACh response was blocked by cobra neurotoxin, D-tubocurarine and atropine.

7. The electrical properties of the myotubes appear to resemble those of normal adult twitch-type skeletal muscle fibres.

8. The pharmacological properties of the myotube cholinergic receptor have been compared with those of the neuromuscular junction and the denervated muscle fibre membrane.

Full text

PDF
751

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AXELSSON J., THESLEFF S. A study of supersensitivity in denervated mammalian skeletal muscle. J Physiol. 1959 Jun 23;147(1):178–193. doi: 10.1113/jphysiol.1959.sp006233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Adrian R. H., Chandler W. K., Hodgkin A. L. Voltage clamp experiments in striated muscle fibres. J Physiol. 1970 Jul;208(3):607–644. doi: 10.1113/jphysiol.1970.sp009139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Beránek R., Vyskocil F. The action of tubocurarine and atropine on the normal and denervated rat diaphragm. J Physiol. 1967 Jan;188(1):53–66. doi: 10.1113/jphysiol.1967.sp008123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DEL CASTILLO J., KATZ B. On the localization of acetylcholine receptors. J Physiol. 1955 Apr 28;128(1):157–181. doi: 10.1113/jphysiol.1955.sp005297. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DIAMOND J., MILEDI R. A study of foetal and new-born rat muscle fibres. J Physiol. 1962 Aug;162:393–408. doi: 10.1113/jphysiol.1962.sp006941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Eaker D., Harris J. B., Thesleff S. Action of a cobra neurotoxin on denervated rat skeletal muscle. Eur J Pharmacol. 1971 Jul;15(2):254–256. doi: 10.1016/0014-2999(71)90182-8. [DOI] [PubMed] [Google Scholar]
  7. Fambrough D., Rash J. E. Development of acetylcholine sensitivity during myogenesis. Dev Biol. 1971 Sep;26(1):55–68. doi: 10.1016/0012-1606(71)90107-2. [DOI] [PubMed] [Google Scholar]
  8. Fedde M. R. Electrical properties and acetylcholine sensitivity of singly and multiply innervated avian muscle fibers. J Gen Physiol. 1969 May;53(5):624–637. doi: 10.1085/jgp.53.5.624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Feltz A., Mallart A. Ionic permeability changes induced by some cholinergic agonists on normal and denervated frog muscles. J Physiol. 1971 Oct;218(1):101–116. doi: 10.1113/jphysiol.1971.sp009606. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fischbach G. D., Nameroff M., Nelson P. G. Electrical properties of chick skeletal muscle fibers developing in cell culture. J Cell Physiol. 1971 Oct;78(2):289–299. doi: 10.1002/jcp.1040780218. [DOI] [PubMed] [Google Scholar]
  11. Fischbach G. D. Synaptic potentials recorded in cell cultures of nerve and muscle. Science. 1970 Sep 25;169(3952):1331–1333. doi: 10.1126/science.169.3952.1331. [DOI] [PubMed] [Google Scholar]
  12. Gainer H. Plasma membrane structure: effects of hydrolases on muscle resting potentials. Biochim Biophys Acta. 1967 Jul 3;135(3):560–562. doi: 10.1016/0005-2736(67)90045-4. [DOI] [PubMed] [Google Scholar]
  13. Grampp W., Harris J. B., Thesleff S. Inhibition of denervation changes in skeletal muscle by blockers of protein synthesis. J Physiol. 1972 Mar;221(3):743–754. doi: 10.1113/jphysiol.1972.sp009780. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Harris J. B., Thesleff S. Studies on tetrodotoxin resistant action potentials in denervated skeletal muscle. Acta Physiol Scand. 1971 Nov;83(3):382–388. doi: 10.1111/j.1748-1716.1971.tb05091.x. [DOI] [PubMed] [Google Scholar]
  15. Kano M., Shimada Y., Ishikawa K. Acetylcholine sensitivity of skeletal muscle cells differentiated in vitro from chick embryo. Brain Res. 1971 Jan 8;25(1):216–219. doi: 10.1016/0006-8993(71)90586-5. [DOI] [PubMed] [Google Scholar]
  16. Karlsson E., Arnberg H., Eaker D. Isolation of the principal neurotoxins of two Naja naja subspecies. Eur J Biochem. 1971 Jul 15;21(1):1–16. doi: 10.1111/j.1432-1033.1971.tb01433.x. [DOI] [PubMed] [Google Scholar]
  17. Lester H. A. Postsynaptic action of cobra toxin at the myoneural junction. Nature. 1970 Aug 15;227(5259):727–728. doi: 10.1038/227727a0. [DOI] [PubMed] [Google Scholar]
  18. Redfern P., Thesleff S. Action potential generation in denervated rat skeletal muscle. II. The action of tetrodotoxin. Acta Physiol Scand. 1971 May;82(1):70–78. doi: 10.1111/j.1748-1716.1971.tb04943.x. [DOI] [PubMed] [Google Scholar]
  19. Robbins N., Yonezawa T. Physiological studies during formation and development of rat neuromuscular junctions in tissue culture. J Gen Physiol. 1971 Oct;58(4):467–481. doi: 10.1085/jgp.58.4.467. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Shimada Y., Kano M. Formation of neuromuscular junctions in embryonic cultures. Arch Histol Jpn. 1971 Jun;33(2):95–114. doi: 10.1679/aohc1950.33.95. [DOI] [PubMed] [Google Scholar]
  21. THESLEFF S. Supersensitivity of skeletal muscle produced by botulinum toxin. J Physiol. 1960 Jun;151:598–607. doi: 10.1113/jphysiol.1960.sp006463. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES