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. 1994 Jan 1;474(1):65–73. doi: 10.1113/jphysiol.1994.sp020003

Effects of activin A on ionic channels in human FSH-secreting tumour cells.

K Takano 1, E Ogata 1, N Yamashita 1
PMCID: PMC1160296  PMID: 7516971

Abstract

1. Effects of activin A on ionic channels were examined in human FSH-secreting tumour cells using electrophysiological techniques. 2. Under voltage clamp with the conventional whole-cell clamp technique, the voltage-gated Na+ channel, the T- and L-type Ca2+ channels, the delayed K+ channel and the A-channel were observed. 3. With the nystatin-perforated whole-cell clamp technique, the same voltage-gated channels were recorded. Activin A (10(-7) M) increased the amplitude of the L-type Ca2+ current, whereas it decreased the amplitude of the delayed K+ current. 4. Under current clamp with the perforated whole-cell clamp technique, more than 80% of the cells exhibited spontaneous action potentials. Application of 10(-7) M activin A depolarized the membrane with a conductance increase and augmented action potential frequency. The reversal potential of the activin A-induced current was -20 to 0 mV. The activin A-induced current was abolished in a Na(+)-free extracellular solution, indicating that the membrane depolarization caused by activin A was due to the conductance increase to Na+ ions through non-selective cation channels.

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Selected References

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  1. Eto Y., Tsuji T., Takezawa M., Takano S., Yokogawa Y., Shibai H. Purification and characterization of erythroid differentiation factor (EDF) isolated from human leukemia cell line THP-1. Biochem Biophys Res Commun. 1987 Feb 13;142(3):1095–1103. doi: 10.1016/0006-291x(87)91528-2. [DOI] [PubMed] [Google Scholar]
  2. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  3. Horn R., Marty A. Muscarinic activation of ionic currents measured by a new whole-cell recording method. J Gen Physiol. 1988 Aug;92(2):145–159. doi: 10.1085/jgp.92.2.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kato M., Suzuki M. Growth hormone releasing factor depolarizes rat pituitary cells in Na+-dependent mechanism. Brain Res. 1989 Jan 2;476(1):145–148. doi: 10.1016/0006-8993(89)91547-3. [DOI] [PubMed] [Google Scholar]
  5. Marchetti C., Childs G. V., Brown A. M. Voltage-dependent calcium currents in rat gonadotropes separated by centrifugal elutriation. Am J Physiol. 1990 Apr;258(4 Pt 1):E589–E596. doi: 10.1152/ajpendo.1990.258.4.E589. [DOI] [PubMed] [Google Scholar]
  6. Mason W. T., Sikdar S. K. Characterization of voltage-gated sodium channels in ovine gonadotrophs: relationship to hormone secretion. J Physiol. 1988 May;399:493–517. doi: 10.1113/jphysiol.1988.sp017093. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Mason W. T., Waring D. W. Electrophysiological recordings from gonadotrophs. Evidence for Ca2+ channels mediated by gonadotrophin-releasing hormone. Neuroendocrinology. 1985 Sep;41(3):258–268. doi: 10.1159/000124186. [DOI] [PubMed] [Google Scholar]
  8. Murata M., Eto Y., Shibai H., Sakai M., Muramatsu M. Erythroid differentiation factor is encoded by the same mRNA as that of the inhibin beta A chain. Proc Natl Acad Sci U S A. 1988 Apr;85(8):2434–2438. doi: 10.1073/pnas.85.8.2434. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Neher E. The influence of intracellular calcium concentration on degranulation of dialysed mast cells from rat peritoneum. J Physiol. 1988 Jan;395:193–214. doi: 10.1113/jphysiol.1988.sp016914. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Schubert D., Kimura H., LaCorbiere M., Vaughan J., Karr D., Fischer W. H. Activin is a nerve cell survival molecule. Nature. 1990 Apr 26;344(6269):868–870. doi: 10.1038/344868a0. [DOI] [PubMed] [Google Scholar]
  11. Stutzin A., Stojilković S. S., Catt K. J., Rojas E. Characteristics of two types of calcium channels in rat pituitary gonadotrophs. Am J Physiol. 1989 Nov;257(5 Pt 1):C865–C874. doi: 10.1152/ajpcell.1989.257.5.C865. [DOI] [PubMed] [Google Scholar]
  12. Takano K., Yamashita N., Kojima I., Kitaoka M., Teramoto A., Ogata E. Effects of activin A and somatostatin on intact FSH secretion and intracellular Ca2+ concentration in human FSH-secreting pituitary adenoma cells. Biochem Biophys Res Commun. 1992 Feb 14;182(3):1408–1415. doi: 10.1016/0006-291x(92)91890-3. [DOI] [PubMed] [Google Scholar]
  13. Totsuka Y., Tabuchi M., Kojima I., Shibai H., Ogata E. A novel action of activin A: stimulation of insulin secretion in rat pancreatic islets. Biochem Biophys Res Commun. 1988 Oct 14;156(1):335–339. doi: 10.1016/s0006-291x(88)80845-3. [DOI] [PubMed] [Google Scholar]
  14. Vale W., Rivier J., Vaughan J., McClintock R., Corrigan A., Woo W., Karr D., Spiess J. Purification and characterization of an FSH releasing protein from porcine ovarian follicular fluid. Nature. 1986 Jun 19;321(6072):776–779. doi: 10.1038/321776a0. [DOI] [PubMed] [Google Scholar]
  15. Yamashita N., Hagiwara S. Membrane depolarization and intracellular Ca2+ increase caused by high external Ca2+ in a rat calcitonin-secreting cell line. J Physiol. 1990 Dec;431:243–267. doi: 10.1113/jphysiol.1990.sp018329. [DOI] [PMC free article] [PubMed] [Google Scholar]

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