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. 1976 Aug 15;158(2):211–221. doi: 10.1042/bj1580211

The effect of intracellular calcium ions on adrenaline-stimulated adenosine 3':5'-cyclic monophosphate concentrations in pigeon erythrocytes, studied by using the ionophore A23187.

A K Campbell, K Siddle
PMCID: PMC1163961  PMID: 186033

Abstract

1. The bivalent cation ionophore A23187 was used to increase the intracellular concentration of Ca2+ in pigeon erythrocytes to investigate whether the increase in cyclic AMP content caused by adrenaline might be influenced by a change in intracellular Ca2+ in intact cells. 2. Incubation of cells with adrenaline, in the concentration range 0.55--55 muM, resulted in an increase in the concentration of cyclic AMP over a period of 60 min. The effect of adrenaline was inhibited by more than 90% with ionophore A23187 (1.9 muM) in the presence of 1 mM-Ca2+. This inhibition could be decreased by decreasing either the concentration of the ionophore or the concentration of extracellular Ca2+, and was independent of the concentration of adrenaline. 3. The effect of ionophore A23187 depended on the time of incubation. Time-course studies showed that maximum inhibition by ionophore A23187 was only observed when the cells were incubated with the ionophore for at least 15 min before the addition of adrenaline. 4. The inhibition by ionophore A23187 depended on the concentration of extracellular Ca2+. In the absence of Mg2+, ionophore A23187 (1.9 muM) inhibited the effect of adrenaline by approx. 30% without added Ca2+, by approx. 66% with 10 muM-Ca2+ and by more than 90% with concentrations of added Ca2+ greater than 30 muM. However, even in the presence of EGTA [ethanedioxybis(ethylamine)tetra-acetate](0.1--10 mM), ionophore A23187 caused an inhibition of the cyclic AMP response of at least 30%, which may have been due to a decrease in cell Mg2+ concentration. 5. The addition of EGTA after incubation of cells with ionophore A23187 resulted in a partial reversal of the inhibition of the effect of adrenaline. 6. Inclusion of Mg2+ (2 mM) in the incubation medium antagonized the inhibitory action of ionophore A23187. This effect was most marked when the ionophore A23187 was added to medium containing Mg2+ before the addition of the cells. 7. The cellular content of Mg2+ was decreased by approx. 50% after 20 min incubation with ionophore A23187 (1.9 muM) in the presence of Ca2+ (1 mM) but no Mg2+. When Mg2+ (2 mM) was also present in the medium, ionophore A23187 caused an increase of approx. 80% in cell Mg2+ content. Ionophore A23187 had no significant effect on cell K+ content. 8. Ionophore A23187 caused a decrease in cell ATP content under some conditions. Since effects on cyclic AMP content could also be shown when ATP was not significanlty lowered, it appeared that a decrease in ATP in the cells could not explain the effect of ionophore A23187 on cyclic AMP. 9. Ionophore A23187 (1.9 muM), with 1 mM-Ca2+, did not enhance cyclic AMP degradation in intact cells, suggesting that the effect of ionophore A23187 on cyclic AMP content was mediated through an inhibition of adenylate cyclase rather than a stimulation of cyclic AMP phosphodiesterase. 10. It was concluded that in intact pigeon erythrocytes adenylate cyclase may be inhibited by intracellular concentrations of Ca2+ in the range 1-10 muM.

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Selected References

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  1. Andersson R., Nilsson K. Cyclic AMP and calcium in relaxation in intestinal smooth muscle. Nat New Biol. 1972 Jul 26;238(82):119–120. doi: 10.1038/newbio238119a0. [DOI] [PubMed] [Google Scholar]
  2. Ashley C. C., Ridgway E. B. Simultaneous recording of membrane potential, calcium transient and tension in single muscle fibers. Nature. 1968 Sep 14;219(5159):1168–1169. doi: 10.1038/2191168a0. [DOI] [PubMed] [Google Scholar]
  3. Baker P. F. Transport and metabolism of calcium ions in nerve. Prog Biophys Mol Biol. 1972;24:177–223. doi: 10.1016/0079-6107(72)90007-7. [DOI] [PubMed] [Google Scholar]
  4. Birnbaumer L. Hormone-sensitive adenylyl cyclases. Useful models for studying hormone receptor functions in cell-free systems. Biochim Biophys Acta. 1973 Sep 10;300(2):129–158. doi: 10.1016/0304-4157(73)90002-6. [DOI] [PubMed] [Google Scholar]
  5. Birnbaumer L., Pohl S. L., Rodbell M. Adenyl cyclase in fat cells. 1. Properties and the effects of adrenocorticotropin and fluoride. J Biol Chem. 1969 Jul 10;244(13):3468–3476. [PubMed] [Google Scholar]
  6. Butcher F. R. The role of calcium and cyclic nucleotides in alpha-amylase release from slices of rat parotid: studies with the divalent cation ionophore A-23187. Metabolism. 1975 Mar;24(3):409–418. doi: 10.1016/0026-0495(75)90120-1. [DOI] [PubMed] [Google Scholar]
  7. Campbell A. K., Dormer R. L. Permeability to calcium of pigeon erythrocyte 'ghosts' studied by using the calcium-activated luminescent protein, obelin. Biochem J. 1975 Nov;152(2):255–265. doi: 10.1042/bj1520255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Campbell A. K. Extraction, partial purification and properties of obelin, the calcium-activated luminescent protein from the hydroid Obelia geniculata. Biochem J. 1974 Nov;143(2):411–418. doi: 10.1042/bj1430411. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Carafoli E. Mitochondrial uptake of calcium ions and the regulation of cell function. Biochem Soc Symp. 1974;(39):89–109. [PubMed] [Google Scholar]
  10. Cohen P. The role of phosphorylase kinase in the nervous and hormonal control of glycogenolysis in muscle. Biochem Soc Symp. 1974;(39):51–73. [PubMed] [Google Scholar]
  11. DAVOREN P. R., SUTHERLAND E. W. THE EFFECT OF L-EPINEPHRINE AND OTHER AGENTS ON THE SYNTHESIS AND RELEASE OF ADENOSINE 3',5'-PHOSPHATE BY WHOLE PIGEON ERYTHROCYTES. J Biol Chem. 1963 Sep;238:3009–3015. [PubMed] [Google Scholar]
  12. Drummond G. I., Duncan L. Adenyl cyclase in cardiac tissue. J Biol Chem. 1970 Mar 10;245(5):976–983. [PubMed] [Google Scholar]
  13. Eimerl S., Savion N., Heichal O., Selinger Z. Induction of enzyme secretion in rat pancreatic slices using the ionophore A-23187 and calcium. An experimental bypass of the hormone receptor pathway. J Biol Chem. 1974 Jun 25;249(12):3991–3993. [PubMed] [Google Scholar]
  14. Entman M. L., Allen J. C., Bornet E. P., Gillette P. C., Wallick E. T., Schwart A. Mechanisms of calcium accumulation and transport in cardiac relaxing system (sarcoplasmic reticulum membranes): effects of Verapamil, D-600, X537A and A23187. J Mol Cell Cardiol. 1972 Dec;4(6):681–687. doi: 10.1016/0022-2828(72)90121-6. [DOI] [PubMed] [Google Scholar]
  15. Entman M. L., Levey G. S., Epstein S. E. Mechanism of action of epinephrine and glucagon on the canine heart. Evidence for increase in sarcotubular calcium stores mediated by cyclic 3',5'-AMP. Circ Res. 1969 Oct;25(4):429–438. doi: 10.1161/01.res.25.4.429. [DOI] [PubMed] [Google Scholar]
  16. Friedmann N., Rasmussen H. Calcium, manganese and hepatic gluconeogenesis. Biochim Biophys Acta. 1970 Oct 27;222(1):41–52. doi: 10.1016/0304-4165(70)90349-1. [DOI] [PubMed] [Google Scholar]
  17. Garcia A. G., Kirpekar S. M., Prat J. C. A calcium ionophore stimulating the secretion of catecholamines from the cat adrenal. J Physiol. 1975 Jan;244(1):253–262. doi: 10.1113/jphysiol.1975.sp010795. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Gardner J. D., Mensh R. S., Kiino D. R., Aurbach G. D. Effects of beta-adrenergic catecholamines on potassium transport in turkey erythrocytes. J Biol Chem. 1975 Feb 25;250(4):1155–1163. [PubMed] [Google Scholar]
  19. Hardman J. G., Beavo J. A., Gray J. P., Chrisman T. D., Patterson W. D., Sutherland E. W. The formation and metabolism of cyclic GMP. Ann N Y Acad Sci. 1971 Dec 30;185:27–35. doi: 10.1111/j.1749-6632.1971.tb45232.x. [DOI] [PubMed] [Google Scholar]
  20. Ho R. J., Sutherland E. W. Formation and release of a hormone antagonist by rat adipocytes. J Biol Chem. 1971 Nov 25;246(22):6822–6827. [PubMed] [Google Scholar]
  21. Kakiuchi S., Yamazaki R., Teshima Y., Uenishi K. Regulation of nucleoside cyclic 3':5'-monophosphate phosphodiesterase activity from rat brain by a modulator and Ca2+. Proc Natl Acad Sci U S A. 1973 Dec;70(12):3526–3530. doi: 10.1073/pnas.70.12.3526. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Levitzki A., Reuben J. Abortive complexes of -amylases with lanthanides. Biochemistry. 1973 Jan 2;12(1):41–44. doi: 10.1021/bi00725a007. [DOI] [PubMed] [Google Scholar]
  23. Oye I., Sutherland E. W. The effect of epinephrine and other agents on adenyl cyclase in the cell membrane of avian erythrocytes. Biochim Biophys Acta. 1966 Oct 31;127(2):347–354. doi: 10.1016/0304-4165(66)90389-8. [DOI] [PubMed] [Google Scholar]
  24. PORTZEHL H., CALDWELL P. C., RUEEGG J. C. THE DEPENDENCE OF CONTRACTION AND RELAXATION OF MUSCLE FIBRES FROM THE CRAB MAIA SQUINADO ON THE INTERNAL CONCENTRATION OF FREE CALCIUM IONS. Biochim Biophys Acta. 1964 May 25;79:581–591. doi: 10.1016/0926-6577(64)90224-4. [DOI] [PubMed] [Google Scholar]
  25. Pfeiffer D. R., Reed P. W., Lardy H. A. Ultraviolet and fluorescent spectral properties of the divalent cation ionophore A23187 and its metal ion complexes. Biochemistry. 1974 Sep 10;13(19):4007–4014. doi: 10.1021/bi00716a029. [DOI] [PubMed] [Google Scholar]
  26. Randle P. J., Denton R. M., Pask H. T., Severson D. L. Calcium ions and the regulation of pyruvate dehydrogenase. Biochem Soc Symp. 1974;(39):75–88. [PubMed] [Google Scholar]
  27. Rasmussen H., Goodman D. B., Tenenhouse A. The role of cyclic AMP and calcium in cell activation. CRC Crit Rev Biochem. 1972 Feb;1(1):95–148. doi: 10.3109/10409237209102545. [DOI] [PubMed] [Google Scholar]
  28. Rasmussen H., Jensen P., Lake W., Friedmann N., Goodman D. B. Cyclic nucleotides and cellular calcium metabolism. Adv Cyclic Nucleotide Res. 1975;5:375–394. [PubMed] [Google Scholar]
  29. Rasmussen H., Tenenhouse A. Cyclic adenosine monophosphate, CA++, and membranes. Proc Natl Acad Sci U S A. 1968 Apr;59(4):1364–1370. doi: 10.1073/pnas.59.4.1364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Reed P. W., Lardy H. A. A23187: a divalent cation ionophore. J Biol Chem. 1972 Nov 10;247(21):6970–6977. [PubMed] [Google Scholar]
  31. Rosen O. M., Goren E. N., Erlichman J., Rosen S. M. Synthesis and degradation of cyclic 3',5'-adenosine monophosphate in frog erythrocytes. Adv Biochem Psychopharmacol. 1970;3:31–50. [PubMed] [Google Scholar]
  32. Rudolph S. A., Greengard P. Regulation of protein phosphorylation and membrane permeability by beta-adrenergic agents and cyclic adenosine 3':5'-monophosphate in the avian erythrocyte. J Biol Chem. 1974 Sep 10;249(17):5684–5687. [PubMed] [Google Scholar]
  33. Scarpa A., Baldassare J., Inesi G. The effect of calcium ionophores on fragmented sarcoplasmic reticulum. J Gen Physiol. 1972 Dec;60(6):735–749. doi: 10.1085/jgp.60.6.735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Schultz G., Hardman J. G., Schultz K., Baird C. E., Sutherland E. W. The importance of calcium ions for the regulation of guanosine 3':5'-cyclic monophosphage levels. Proc Natl Acad Sci U S A. 1973 Dec;70(12):3889–3893. doi: 10.1073/pnas.70.12.3889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Selinger Z., Eimerl S., Schramm M. A calcium ionophore simulating the action of epinephrine on the alpha-adrenergic receptor. Proc Natl Acad Sci U S A. 1974 Jan;71(1):128–131. doi: 10.1073/pnas.71.1.128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Shimomura O., Johnson F. H. Further data on the specificity of aequorin luminescence to calcium. Biochem Biophys Res Commun. 1973 Jul 17;53(2):490–494. doi: 10.1016/0006-291x(73)90688-8. [DOI] [PubMed] [Google Scholar]
  37. Siddle K., Hales C. N. Hormonal control of adipose tissue lipolysis. Proc Nutr Soc. 1975 Dec;34(3):233–239. doi: 10.1079/pns19750044. [DOI] [PubMed] [Google Scholar]
  38. Siddle K., Kane-Maguire B., Campbell A. K. The effects of glucagon and insulin on adenosine 3':5'-cyclic monophosphate concentrations in an organ culture of mature rat liver. Biochem J. 1973 Apr;132(4):765–773. doi: 10.1042/bj1320765. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Steer M. L., Levitzki A. The control of adenylate cyclase by calcium in turkey erythrocyte ghosts. J Biol Chem. 1975 Mar 25;250(6):2080–2084. [PubMed] [Google Scholar]
  40. Steer M. L., Levitzki A. The interaction of catecholamines, Ca2+ and adenylate cyclase in the intact turkey erythrocyte. Arch Biochem Biophys. 1975 Mar;167(1):371–376. doi: 10.1016/0003-9861(75)90473-7. [DOI] [PubMed] [Google Scholar]
  41. Steiner A. L., Kipnis D. M., Utiger R., Parker C. Radioimmunoassay for the measurement of adenosine 3',5'-cyclic phosphate. Proc Natl Acad Sci U S A. 1969 Sep;64(1):367–373. doi: 10.1073/pnas.64.1.367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Steinhardt R. A., Epel D., Carroll E. J., Jr, Yanagimachi R. Is calcium ionophore a universal activator for unfertilised eggs? Nature. 1974 Nov 1;252(5478):41–43. doi: 10.1038/252041a0. [DOI] [PubMed] [Google Scholar]
  43. Teo T. S., Wang J. H. Mechanism of activation of a cyclic adenosine 3':5'-monophosphate phosphodiesterase from bovine heart by calcium ions. Identification of the protein activator as a Ca2+ binding protein. J Biol Chem. 1973 Sep 10;248(17):5950–5955. [PubMed] [Google Scholar]
  44. Weller M., Rodnight R. Protein kinase activity stimulated by adenosine 3' :5'-cyclic monophosphate in synaptic-membrane fragments from ox brain. Inhibition of intrinsic activity by free and membrane-bound calcium ions. Biochem J. 1974 Sep;142(3):605–609. doi: 10.1042/bj1420605. [DOI] [PMC free article] [PubMed] [Google Scholar]

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