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. 1975 Jan;244(1):129–143. doi: 10.1113/jphysiol.1975.sp010787

Developmental changes of membrane electrical properties in a rat skeletal muscle cell line.

Y Kidokoro
PMCID: PMC1330748  PMID: 1168256

Abstract

1. The developmental changes of the cell membrane electrical properties were studied with micro-electrodes in a rat skeletal muscle cell line. 2. The resting potentials in myoblasts were minus 71 plus or minus 3 mV (mean plus or minus S.D.) and those in myotubes which were formed by fusion of myoblasts were minus 69 plus or minus 3 mV. There was no developmental change in the resting potential during the period examined. 3. The ionic mechanism for the resting potential was the same in myoblasts and myotubes. The resting membrane was almost exclusively permeable to K ions, while permeability to Na ions was not detectable. There was a small permeability to Cl ions. 4. The specific membrane resistance and capacitance were 8 k omega. cm-2 and 1 muF/cm-2 for myoblasts and 12 k omege. cm-2 and 5 muF/cm-2 for myotubes, respectively. 5. Action potentials in myoblasts were evoked by anode break stimulation. They were small and did not overshoot zero membrane potential. The action potentials in myotubes were larger, and had an average overshoot of 32 plus or minus 7 mV and a maximum rate of rise of 93 plus or minus 28 V/sec. 6. The current-voltage relation was examined. Delayed rectification was found in myotubes but not in myoblasts.

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Selected References

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

  1. Albuquerque E. X., Thesleff S. A comparative study of membrane properties of innervated and chronically denervated fast and slow skeletal muscles of the rat. Acta Physiol Scand. 1968 Aug;73(4):471–480. doi: 10.1111/j.1365-201x.1968.tb10886.x. [DOI] [PubMed] [Google Scholar]
  2. Boethius J., Knutsson E. Resting membrane potential in chick muscle cells during ontogeny. J Exp Zool. 1970 Jul;174(3):281–286. doi: 10.1002/jez.1401740304. [DOI] [PubMed] [Google Scholar]
  3. Bryant S. H., Morales-Aguilera A. Chloride conductance in normal and myotonic muscle fibres and the action of monocarboxylic aromatic acids. J Physiol. 1971 Dec;219(2):367–383. doi: 10.1113/jphysiol.1971.sp009667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. 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]
  5. 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]
  6. HODGKIN A. L., HOROWICZ P. The effect of sudden changes in ionic concentrations on the membrane potential of single muscle fibres. J Physiol. 1960 Sep;153:370–385. doi: 10.1113/jphysiol.1960.sp006540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hagiwara S., Toyama K., Hayashi H. Mechanisms of anion and cation permeations in the resting membrane of a barnacle muscle fiber. J Gen Physiol. 1971 Apr;57(4):408–434. doi: 10.1085/jgp.57.4.408. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Harris A. J., Heinemann S., Schubert D., Tarakis H. Trophic interaction between cloned tissue culture lines of nerve and muscle. Nature. 1971 Jun 4;231(5301):296–301. doi: 10.1038/231296a0. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. Hutter O. F., Warner A. E. The pH sensitivity of the chloride conductance of frog skeletal muscle. J Physiol. 1967 Apr;189(3):403–425. doi: 10.1113/jphysiol.1967.sp008176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kidokoro Y. Development of action potentials in a clonal rat skeletal muscle cell line. Nat New Biol. 1973 Jan 31;241(109):158–159. doi: 10.1038/newbio241158a0. [DOI] [PubMed] [Google Scholar]
  12. Miyazaki S., Takahashi K., Tsuda K. Calcium and sodium contributions to regenerative responses in the embryonic excitable cell membrane. Science. 1972 Jun 30;176(4042):1441–1443. doi: 10.1126/science.176.4042.1441. [DOI] [PubMed] [Google Scholar]
  13. NAKAJIMA S., IWASAKI S., OBATA K. Delayed rectification and anomalous rectification in frog's skeletal muscle membrane. J Gen Physiol. 1962 Sep;46:97–115. doi: 10.1085/jgp.46.1.97. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Powell J. A., Fambrough D. M. Electrical properties of normal and dysgenic mouse skeletal muscle in culture. J Cell Physiol. 1973 Aug;82(1):21–38. doi: 10.1002/jcp.1040820104. [DOI] [PubMed] [Google Scholar]
  15. Redfern P., Thesleff S. Action potential generation in denervated rat skeletal muscle. I. Quantitative aspects. Acta Physiol Scand. 1971 Apr;81(4):557–564. doi: 10.1111/j.1748-1716.1971.tb04932.x. [DOI] [PubMed] [Google Scholar]
  16. Schubert D., Tarikas H., Humphreys S., Heinemann S., Patrick J. Protein synthesis and secretion in a myogenic cell line. Dev Biol. 1973 Jul;33(1):18–37. doi: 10.1016/0012-1606(73)90161-9. [DOI] [PubMed] [Google Scholar]
  17. Stefani E., Steinbach A. B. Resting potential and electrical properties of frog slow muscle fibres. Effect of different external solutions. J Physiol. 1969 Aug;203(2):383–401. doi: 10.1113/jphysiol.1969.sp008869. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Takahashi K., Miyazaki S. I., Kidokoro Y. Development of excitability in embryonic muscle cell membranes in certain tunicates. Science. 1971 Jan 29;171(3969):415–418. doi: 10.1126/science.171.3969.415. [DOI] [PubMed] [Google Scholar]
  19. VOGT M., DULBECCO R. Steps in the neoplastic transformation of hamster embryo cells by polyoma virus. Proc Natl Acad Sci U S A. 1963 Feb 15;49:171–179. doi: 10.1073/pnas.49.2.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. WEIDMANN S. The electrical constants of Purkinje fibres. J Physiol. 1952 Nov;118(3):348–360. doi: 10.1113/jphysiol.1952.sp004799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Yaffe D. Retention of differentiation potentialities during prolonged cultivation of myogenic cells. Proc Natl Acad Sci U S A. 1968 Oct;61(2):477–483. doi: 10.1073/pnas.61.2.477. [DOI] [PMC free article] [PubMed] [Google Scholar]

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