Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1984 Jul 1;99(1 Pt 1):83–87. doi: 10.1083/jcb.99.1.83

Thyrotropin-releasing hormone increases cytosolic free Ca2+ in clonal pituitary cells (GH3 cells): direct evidence for the mobilization of cellular calcium

PMCID: PMC2275624  PMID: 6429159

Abstract

Changes in the cytosolic free Ca2+ concentration following cell surface receptor activation have been proposed to mediate a wide variety of cellular responses. Using the specific Ca2+ chelator quin2 as a fluorescent intracellular probe, we measured the Ca2+ levels in the cytosol of clonal rat pituitary cells, GH3 cells. We demonstrate that thyrotropin-releasing hormone (TRH) at nanomolar concentrations leads to a rapid and transient increase in cytosolic Ca2+. This increase was found to occur in Ca2+-free media in the presence of EGTA, thus at extracellular Ca2+ levels that are below the cytosolic concentrations, and was not prevented by verapamil, a Ca2+ channel blocker. Depolarization of GH3 cells with K+, which can mimic the action of TRH on prolactin release, increased cytosolic Ca2+ levels only in the presence of free extracellular Ca2+, and this increase could be blocked by verapamil. These data show that the mobilization of intracellular Ca2+ due to TRH action that has been proposed by previous studies actually leads to an increase in cytosolic free Ca2+. The kinetic features of this response emphasize the key role of cytosolic free Ca2+ in stimulus-secretion coupling.

Full Text

The Full Text of this article is available as a PDF (544.1 KB).

Selected References

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

  1. Borle A. B., Snowdowne K. W. Measurement of intracellular free calcium in monkey kidney cells with aequorin. Science. 1982 Jul 16;217(4556):252–254. doi: 10.1126/science.6806904. [DOI] [PubMed] [Google Scholar]
  2. Drust D. S., Martin T. F. Thyrotropin-releasing hormone rapidly and transiently stimulates cytosolic calcium-dependent protein phosphorylation in GH3 pituitary cells. J Biol Chem. 1982 Jul 10;257(13):7566–7573. [PubMed] [Google Scholar]
  3. Dufy B., Vincent J. D., Fleury H., Du Pasquier P., Gourdji D., Tixier-Vidal A. Membrane effects of thyrotropin-releasing hormone and estrogen shown by intracellular recording from pituitary cells. Science. 1979 May 4;204(4392):509–511. doi: 10.1126/science.107590. [DOI] [PubMed] [Google Scholar]
  4. Gershengorn M. C., Hoffstein S. T., Rebecchi M. J., Geras E., Rubin B. G. Thyrotropin-releasing hormone stimulation of prolactin release from clonal rat pituitary cells: evidence for action independent of extracellular calcium. J Clin Invest. 1981 Jun;67(6):1769–1776. doi: 10.1172/JCI110216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gershengorn M. C. Thyrotropin releasing hormone stimulation of prolactin release. Evidence for a membrane potential-independent, Ca2+-dependent mechanism of action. J Biol Chem. 1980 Mar 10;255(5):1801–1803. [PubMed] [Google Scholar]
  6. Gershengorn M. C. Thyrotropin releasing hormone. A review of the mechanisms of acute stimulation of pituitary hormone release. Mol Cell Biochem. 1982 Jun 25;45(3):163–179. doi: 10.1007/BF00230085. [DOI] [PubMed] [Google Scholar]
  7. Hesketh T. R., Smith G. A., Moore J. P., Taylor M. V., Metcalfe J. C. Free cytoplasmic calcium concentration and the mitogenic stimulation of lymphocytes. J Biol Chem. 1983 Apr 25;258(8):4876–4882. [PubMed] [Google Scholar]
  8. Kidokoro Y. Spontaneous calcium action potentials in a clonal pituitary cell line and their relationship to prolactin secretion. Nature. 1975 Dec 25;258(5537):741–742. doi: 10.1038/258741a0. [DOI] [PubMed] [Google Scholar]
  9. Lee C. O., Taylor A., Windhager E. E. Cytosolic calcium ion activity in epithelial cells of Necturus kidney. Nature. 1980 Oct 30;287(5785):859–861. doi: 10.1038/287859a0. [DOI] [PubMed] [Google Scholar]
  10. O'Doherty J., Youmans S. J., Armstrong W. M., Stark R. J. Calcium regulation during stimulus-secretion coupling: continuous measurement of intracellular calcium activities. Science. 1980 Jul 25;209(4455):510–513. doi: 10.1126/science.7394518. [DOI] [PubMed] [Google Scholar]
  11. Ostlund R. E., Jr, Leung J. T., Hajek S. V., Winokur T., Melman M. Acute stimulated hormone release from cultured GH3 pituitary cells. Endocrinology. 1978 Oct;103(4):1245–1252. doi: 10.1210/endo-103-4-1245. [DOI] [PubMed] [Google Scholar]
  12. Ozawa S. Biphasic effect of thyrotropin-releasing hormone on membrane K+ permeability in rat clonal pituitary cells. Brain Res. 1981 Mar 23;209(1):240–244. doi: 10.1016/0006-8993(81)91188-4. [DOI] [PubMed] [Google Scholar]
  13. Pozzan T., Lew D. P., Wollheim C. B., Tsien R. Y. Is cytosolic ionized calcium regulating neutrophil activation? Science. 1983 Sep 30;221(4618):1413–1415. doi: 10.1126/science.6310757. [DOI] [PubMed] [Google Scholar]
  14. Rebecchi M. J., Gerry R. H., Gershengorn M. C. Thyrotropin-releasing hormone causes loss of cellular calcium without calcium uptake by rat pituitary cells in culture. Studies using arsenazo III for direct measurement of calcium. J Biol Chem. 1982 Mar 25;257(6):2751–2753. [PubMed] [Google Scholar]
  15. Rink T. J., Montecucco C., Hesketh T. R., Tsien R. Y. Lymphocyte membrane potential assessed with fluorescent probes. Biochim Biophys Acta. 1980;595(1):15–30. doi: 10.1016/0005-2736(80)90243-6. [DOI] [PubMed] [Google Scholar]
  16. Rink T. J., Smith S. W., Tsien R. Y. Cytoplasmic free Ca2+ in human platelets: Ca2+ thresholds and Ca-independent activation for shape-change and secretion. FEBS Lett. 1982 Nov 1;148(1):21–26. doi: 10.1016/0014-5793(82)81234-9. [DOI] [PubMed] [Google Scholar]
  17. Ronning S. A., Heatley G. A., Martin T. F. Thyrotropin-releasing hormone mobilizes Ca2+ from endoplasmic reticulum and mitochondria of GH3 pituitary cells: characterization of cellular Ca2+ pools by a method based on digitonin permeabilization. Proc Natl Acad Sci U S A. 1982 Oct;79(20):6294–6298. doi: 10.1073/pnas.79.20.6294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Schrey M. P., Brown B. L., Ekins R. P. Studies on the role of calcium and cyclic nucleotides in the control of TSH secretion. Mol Cell Endocrinol. 1978 Sep;11(3):249–264. doi: 10.1016/0303-7207(78)90012-6. [DOI] [PubMed] [Google Scholar]
  19. Tan K. N., Tashjian A. H., Jr Receptor-mediated release of plasma membrane-associated calcium and stimulation of calcium uptake by thyrotropin-releasing hormone in pituitary cells in culture. J Biol Chem. 1981 Sep 10;256(17):8994–9002. [PubMed] [Google Scholar]
  20. Taraskevich P. S., Douglas W. W. Action potentials occur in cells of the normal anterior pituitary gland and are stimulated by the hypophysiotropic peptide thyrotropin-releasing hormone. Proc Natl Acad Sci U S A. 1977 Sep;74(9):4064–4067. doi: 10.1073/pnas.74.9.4064. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Tashjian A. H., Jr Clonal strains of hormone-producing pituitary cells. Methods Enzymol. 1979;58:527–535. doi: 10.1016/s0076-6879(79)58167-1. [DOI] [PubMed] [Google Scholar]
  22. Tsien R. Y. New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures. Biochemistry. 1980 May 27;19(11):2396–2404. doi: 10.1021/bi00552a018. [DOI] [PubMed] [Google Scholar]
  23. Tsien R. Y., Pozzan T., Rink T. J. Calcium homeostasis in intact lymphocytes: cytoplasmic free calcium monitored with a new, intracellularly trapped fluorescent indicator. J Cell Biol. 1982 Aug;94(2):325–334. doi: 10.1083/jcb.94.2.325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Wollheim C. B., Pozzan T. Correlation between cytosolic free Ca2+ and insulin release in an insulin-secreting cell line. J Biol Chem. 1984 Feb 25;259(4):2262–2267. [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES