Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1989 Nov;98(3):809–816. doi: 10.1111/j.1476-5381.1989.tb14609.x

Thapsigargin, a new calcium-dependent epithelial anion secretagogue.

D J Brayden 1, M R Hanley 1, O Thastrup 1, A W Cuthbert 1
PMCID: PMC1854789  PMID: 2511993

Abstract

1. Thapsigargin, a sesquiterpene lactone, was shown to cause electrogenic anion secretion in monolayers of human colonic epithelial cells, an effect which was crucially dependent upon calcium and did not involve eicosanoid formation. 2. To measure the secretory effect calcium needed to be present in the external bathing solution. By means of Fura-2 fluorescence measurements thapsigargin was shown to raise Cai by around 250 nM when the bathing solution contained calcium. In the nominal absence of external calcium thapsigargin raised Cai by only 60 nM, but from a lower basal value. This was insufficient to cause secretion. 3. Effects of other calcium-dependent secretagogues (e.g. lysylbradykinin) were inhibited in the presence of thapsigargin, whereas kinin responses were potentiated if the peptide was added following a stimulus which increases cyclic AMP. 4. From the data given here and the known behaviour of colonic epithelia it is concluded that thapsigargin increases Cai by a non-ionophoric mechanism by release from internal stores. Calcium-stimulated calcium influx then follows resulting in the opening of basolateral K channels, increasing the electrochemical gradient for chloride efflux, or alternatively by activating anion channels in the apical membrane. It is concluded that thapsigargin is a potentially important tool for examining epithelial mechanisms.

Full text

PDF
809

Selected References

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

  1. Cartwright C. A., McRoberts J. A., Mandel K. G., Dharmsathaphorn K. Synergistic action of cyclic adenosine monophosphate- and calcium-mediated chloride secretion in a colonic epithelial cell line. J Clin Invest. 1985 Nov;76(5):1837–1842. doi: 10.1172/JCI112176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cuthbert A. W. Calcium-dependent chloride secretion in rat colon epithelium. J Physiol. 1985 Apr;361:1–17. doi: 10.1113/jphysiol.1985.sp015629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cuthbert A. W., Egléme C., Greenwood H., Hickman M. E., Kirkland S. C., MacVinish L. J. Calcium- and cyclic AMP-dependent chloride secretion in human colonic epithelia. Br J Pharmacol. 1987 Jul;91(3):503–515. doi: 10.1111/j.1476-5381.1987.tb11243.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cuthbert A. W., Kirkland S. C., MacVinish L. J. Kinin effects on ion transport in monolayers of HCA-7 cells, a line from a human colonic adenocarcinoma. Br J Pharmacol. 1985 Sep;86(1):3–5. doi: 10.1111/j.1476-5381.1985.tb09428.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dharmsathaphorn K., Pandol S. J. Mechanism of chloride secretion induced by carbachol in a colonic epithelial cell line. J Clin Invest. 1986 Feb;77(2):348–354. doi: 10.1172/JCI112311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Erlij D., Gersten L., Sterba G., Schoen H. F. Role of prostaglandin release in the response of tight epithelia to Ca2+ ionophores. Am J Physiol. 1986 Apr;250(4 Pt 1):C629–C636. doi: 10.1152/ajpcell.1986.250.4.C629. [DOI] [PubMed] [Google Scholar]
  7. Frizzell R. A. Active chloride secretion by rabbit colon: calcium-dependent stimulation by ionophore A23187. J Membr Biol. 1977 Jun 30;35(2):175–187. doi: 10.1007/BF01869948. [DOI] [PubMed] [Google Scholar]
  8. Hanley M. R., Jackson T. R., Cheung W. T., Dreher M., Gatti A., Hawkins P., Patterson S. I., Vallejo M., Dawson A. P., Thastrup O. Molecular mechanisms of phospholipid signaling pathways in mammalian nerve cells. Cold Spring Harb Symp Quant Biol. 1988;53(Pt 1):435–445. doi: 10.1101/sqb.1988.053.01.051. [DOI] [PubMed] [Google Scholar]
  9. Hanley M. R., Jackson T. R., Vallejo M., Patterson S. I., Thastrup O., Lightman S., Rogers J., Henderson G., Pini A. Neural function: metabolism and actions of inositol metabolites in mammalian brain. Philos Trans R Soc Lond B Biol Sci. 1988 Jul 26;320(1199):381–398. doi: 10.1098/rstb.1988.0083. [DOI] [PubMed] [Google Scholar]
  10. Jackson T. R., Patterson S. I., Thastrup O., Hanley M. R. A novel tumour promoter, thapsigargin, transiently increases cytoplasmic free Ca2+ without generation of inositol phosphates in NG115-401L neuronal cells. Biochem J. 1988 Jul 1;253(1):81–86. doi: 10.1042/bj2530081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kirkland S. C. Dome formation by a human colonic adenocarcinoma cell line (HCA-7). Cancer Res. 1985 Aug;45(8):3790–3795. [PubMed] [Google Scholar]
  12. Ohuchi K., Sugawara T., Watanabe M., Hirasawa N., Tsurufuji S., Fujiki H., Christensen S. B., Sugimura T. Analysis of the stimulative effect of thapsigargin, a non-TPA-type tumour promoter, on arachidonic acid metabolism in rat peritoneal macrophages. Br J Pharmacol. 1988 Jul;94(3):917–923. doi: 10.1111/j.1476-5381.1988.tb11604.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ohuchi K., Sugawara T., Watanabe M., Hirasawa N., Tsurufuji S., Fujiki H., Sugimura T., Christensen S. B. Stimulation of arachidonic acid metabolism in rat peritoneal macrophages by thapsigargin, a non-(12-O-tetradecanoylphorbol-13-acetate) (TPA)-type tumor promoter. J Cancer Res Clin Oncol. 1987;113(4):319–324. doi: 10.1007/BF00397715. [DOI] [PubMed] [Google Scholar]
  14. Poenie M., Alderton J., Tsien R. Y., Steinhardt R. A. Changes of free calcium levels with stages of the cell division cycle. Nature. 1985 May 9;315(6015):147–149. doi: 10.1038/315147a0. [DOI] [PubMed] [Google Scholar]
  15. Putney J. W., Jr A model for receptor-regulated calcium entry. Cell Calcium. 1986 Feb;7(1):1–12. doi: 10.1016/0143-4160(86)90026-6. [DOI] [PubMed] [Google Scholar]
  16. Smith P. L., McCabe R. D. A23187-induced changes in colonic K and Cl transport are mediated by separate mechanisms. Am J Physiol. 1984 Dec;247(6 Pt 1):G695–G702. doi: 10.1152/ajpgi.1984.247.6.G695. [DOI] [PubMed] [Google Scholar]
  17. Smith P. L., Welsh M. J., Stoff J. S., Frizzell R. A. Chloride secretion by canine tracheal epithelium: I. Role of intracellular c AMP levels. J Membr Biol. 1982;70(3):217–226. doi: 10.1007/BF01870564. [DOI] [PubMed] [Google Scholar]
  18. Thastrup O., Foder B., Scharff O. The calcium mobilizing tumor promoting agent, thapsigargin elevates the platelet cytoplasmic free calcium concentration to a higher steady state level. A possible mechanism of action for the tumor promotion. Biochem Biophys Res Commun. 1987 Feb 13;142(3):654–660. doi: 10.1016/0006-291x(87)91464-1. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES