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. 1996 Jul;118(6):1327–1334. doi: 10.1111/j.1476-5381.1996.tb15541.x

Dual regulation of the Na+/H(+)-exchange in rat peritoneal mast cells: role of protein kinase C and calcium on pHi regulation and histamine release.

U G Friis 1, T Johansen 1
PMCID: PMC1909654  PMID: 8832053

Abstract

1. The purpose of this study was to compare the actions of phorbol 12-myristate 13-acetate (PMA) and ionomycin on Na+/H+ exchange activation and histamine release to that of compound 48/80 in order to study the possible relationship between pHi and secretion of histamine in rat peritoneal mast cells. 2. Resting pHi in mast cells suspended in a bicarbonate-free physiological salt solution amounted to 6.73 +/- 0.05 (mean +/- s.d., n = 52). 3. PMA (20 nM) induced a substantial but rather slow increase in pHi. This response was very sensitive to inhibition by staurosporine, very sensitive to inhibition by 5-(N,N-hexamethylene)amiloride (HMA), insensitive to the absence of extracellular calcium (without EGTA), and sensitive to partial depletion of intracellular calcium with EGTA. 4. Ionomycin (1 microM) induced a biphasic change in pHi that was sensitive to inhibition by HMA, insensitive to staurosporine. In the absence of extracellular calcium using EGTA, the biphasic response disappeared, leaving only a slow, and diminished change in pHi. 5. The effects of ionomycin and PMA on pHi were additive. 6. Addition of the secretagogue compound 48/80 (1 microgram ml-1) increased pHi, substantially, delta pHi amounting to 0.29 +/- 0.05 pH-units (n = 4). The biphasic pHi-response was insensitive to the absence of extracellular calcium (without EGTA). The initial fast response in pHi was, however, inhibited by HMA, not staurosporine. 7. The finding that staurosporine and HMA each inhibited approximately half of the compound 48/80-induced pHi-response, whereas both inhibitors completely abolished the compound 48/80-induced pHi-response seems to indicate that two independent pathways for the activation of the Na+/H+ exchange were stimulated by compound 48/80. 8. The histamine release induced via both PKC activation (using PMA) and calcium (using ionomycin) were much larger than the sum of each activation pathway, whereas in the absence of extracellular calcium using EGTA, the histamine release in response to PMA and ionomycin was completely abolished. 9. The compound 48/80-induced histamine release was partially sensitive to inhibition by HMA (approximately 30% inhibition) and partially sensitive to inhibition by staurosporine (approximately 50% inhibition). Preincubation with staurosporine and HMA before stimulation with compound 48/80 showed the same degree of inhibition as observed after staurosporine alone, even though this combination of drugs completely inhibited the pHi-response. Furthermore, compound 48/80-induced histamine release was not dependent on the presence of extracellular calcium (with and without EGTA). 10. In spite of the similarities in second messenger pathways for pHi regulation and histamine release, it is, however, not very likely that these two processes are directly related. It is, however, possible, that an increase in pHi plays a permissive, rather than an essential role for histamine release in rat peritoneal mast cells. This hypothesis was supported by the finding that preincubation with the Na+/H+ exchange-inhibitor HMA inhibited 30% of the compound 48/80-induced histamine secretion.

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Selected References

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  1. Alfonso A., Botana M. A., Vieytes M. R., Botana L. M. Functional characterization of the Na(+)-H+ exchanger in rat mast cells: crosstalks between different kinase pathways. Eur J Pharmacol. 1994 May 17;267(3):289–296. doi: 10.1016/0922-4106(94)90153-8. [DOI] [PubMed] [Google Scholar]
  2. Alfonso A., Botana M. A., Vieytes M. R., Louzao M. C., Botana L. M. Effect of signal transduction pathways on the action of thapsigargin on rat mast cells. Crosstalks between cellular signalling and cytosolic pH. Biochem Pharmacol. 1994 May 18;47(10):1813–1820. doi: 10.1016/0006-2952(94)90310-7. [DOI] [PubMed] [Google Scholar]
  3. Ali H., Collado-Escobar D. M., Beaven M. A. The rise in concentration of free Ca2+ and of pH provides sequential, synergistic signals for secretion in antigen-stimulated rat basophilic leukemia (RBL-2H3) cells. J Immunol. 1989 Oct 15;143(8):2626–2633. [PubMed] [Google Scholar]
  4. Alvarez J., García-Sancho J., Mollinedo F., Sanchez A. Intracellular Ca2+ potentiates Na+/H+ exchange and cell differentiation induced by phorbol ester in U937 cells. Eur J Biochem. 1989 Aug 15;183(3):709–714. doi: 10.1111/j.1432-1033.1989.tb21102.x. [DOI] [PubMed] [Google Scholar]
  5. Chakravarty N., Kjeldsen B., Hansen M., Nielsen E. H. The involvement of protein kinase C in exocytosis in mast cells. Exp Cell Res. 1990 Feb;186(2):245–249. doi: 10.1016/0014-4827(90)90302-q. [DOI] [PubMed] [Google Scholar]
  6. Chakravarty N. The role of protein kinase C in histamine secretion from mast cells. Acta Physiol Scand. 1990 Jun;139(2):319–331. doi: 10.1111/j.1748-1716.1990.tb08930.x. [DOI] [PubMed] [Google Scholar]
  7. Chakravarty N. The roles of calmodulin and protein kinase C in histamine secretion from mast cells. Agents Actions. 1992 Jul;36(3-4):183–191. [PubMed] [Google Scholar]
  8. Choi O. H., Adelstein R. S., Beaven M. A. Secretion from rat basophilic RBL-2H3 cells is associated with diphosphorylation of myosin light chains by myosin light chain kinase as well as phosphorylation by protein kinase C. J Biol Chem. 1994 Jan 7;269(1):536–541. [PubMed] [Google Scholar]
  9. Graham C. S., Tashjian A. H., Jr Mechanisms of activation of Na+/H+ exchange in human osteoblast-like SaOS-2 cells. Biochem J. 1992 Nov 15;288(Pt 1):137–143. doi: 10.1042/bj2880137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Grosman N. Influence of staurosporine, a more selective derivative CGP 41,251 and an inactive analogue CGP 42,700 on histamine release from isolated rat mast cells. Immunopharmacology. 1992 Jul-Aug;24(1):47–55. doi: 10.1016/0162-3109(92)90069-o. [DOI] [PubMed] [Google Scholar]
  11. Guse A. H., Roth E., Emmrich F. Ca2+ release and Ca2+ entry induced by rapid cytosolic alkalinization in Jurkat T-lymphocytes. Biochem J. 1994 Jul 1;301(Pt 1):83–88. doi: 10.1042/bj3010083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Izushi K., Tasaka K. Ca(2+)-induced translocation of protein kinase C during Ca(2+)-dependent histamine release from beta-escin-permeabilized rat mast cells. Pharmacology. 1992;44(2):61–70. doi: 10.1159/000138874. [DOI] [PubMed] [Google Scholar]
  13. Johansen T., Knudsen T., Bertelsen H. Reversal by EGTA of the enhanced secretory responsiveness of mast cells due to treatment with ouabain. FEBS Lett. 1990 Mar 26;262(2):228–230. doi: 10.1016/0014-5793(90)80196-p. [DOI] [PubMed] [Google Scholar]
  14. Katakami Y., Kaibuchi K., Sawamura M., Takai Y., Nishizuka Y. Synergistic action of protein kinase C and calcium for histamine release from rat peritoneal mast cells. Biochem Biophys Res Commun. 1984 Jun 15;121(2):573–578. doi: 10.1016/0006-291x(84)90220-1. [DOI] [PubMed] [Google Scholar]
  15. Kazanietz M. G., Krausz K. W., Blumberg P. M. Differential irreversible insertion of protein kinase C into phospholipid vesicles by phorbol esters and related activators. J Biol Chem. 1992 Oct 15;267(29):20878–20886. [PubMed] [Google Scholar]
  16. Koopmann W. R., Jr, Jackson R. C. Calcium- and guanine-nucleotide-dependent exocytosis in permeabilized rat mast cells. Modulation by protein kinase C. Biochem J. 1990 Jan 15;265(2):365–373. doi: 10.1042/bj2650365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kurosawa M., Kobayashi S. Changes in protein kinase C activity during histamine release from activated rat mast cells. Allergy. 1989 Apr;44(3):226–232. doi: 10.1111/j.1398-9995.1989.tb02267.x. [DOI] [PubMed] [Google Scholar]
  18. Linnebjerg H., Hansen H. S., Jensen B. Effect of amiloride on arachidonic acid and histamine release from rat mast cells. Agents Actions. 1989 Apr;27(1-2):39–42. doi: 10.1007/BF02222192. [DOI] [PubMed] [Google Scholar]
  19. Morgan A. J., Jacob R. Ionomycin enhances Ca2+ influx by stimulating store-regulated cation entry and not by a direct action at the plasma membrane. Biochem J. 1994 Jun 15;300(Pt 3):665–672. doi: 10.1042/bj3000665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Noël J., Pouysségur J. Hormonal regulation, pharmacology, and membrane sorting of vertebrate Na+/H+ exchanger isoforms. Am J Physiol. 1995 Feb;268(2 Pt 1):C283–C296. doi: 10.1152/ajpcell.1995.268.2.C283. [DOI] [PubMed] [Google Scholar]
  21. Penner R. Multiple signaling pathways control stimulus-secretion coupling in rat peritoneal mast cells. Proc Natl Acad Sci U S A. 1988 Dec;85(24):9856–9860. doi: 10.1073/pnas.85.24.9856. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Razin E., Pecht I., Rivera J. Signal transduction in the activation of mast cells and basophils. Immunol Today. 1995 Aug;16(8):370–373. doi: 10.1016/0167-5699(95)80003-4. [DOI] [PubMed] [Google Scholar]
  23. Rink T. J., Tsien R. Y., Pozzan T. Cytoplasmic pH and free Mg2+ in lymphocytes. J Cell Biol. 1982 Oct;95(1):189–196. doi: 10.1083/jcb.95.1.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Rodríguez Del Castillo A., Vitale M. L., Trifaró J. M. Ca2+ and pH determine the interaction of chromaffin cell scinderin with phosphatidylserine and phosphatidylinositol 4,5,-biphosphate and its cellular distribution during nicotinic-receptor stimulation and protein kinase C activation. J Cell Biol. 1992 Nov;119(4):797–810. doi: 10.1083/jcb.119.4.797. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. SHORE P. A., BURKHALTER A., COHN V. H., Jr A method for the fluorometric assay of histamine in tissues. J Pharmacol Exp Ther. 1959 Nov;127:182–186. [PubMed] [Google Scholar]
  26. Sagi-Eisenberg R., Lieman H., Pecht I. Protein kinase C regulation of the receptor-coupled calcium signal in histamine-secreting rat basophilic leukaemia cells. Nature. 1985 Jan 3;313(5997):59–60. doi: 10.1038/313059a0. [DOI] [PubMed] [Google Scholar]
  27. Slater S. J., Kelly M. B., Taddeo F. J., Rubin E., Stubbs C. D. Evidence for discrete diacylglycerol and phorbol ester activator sites on protein kinase C. Differences in effects of 1-alkanol inhibition, activation by phosphatidylethanolamine and calcium chelation. J Biol Chem. 1994 Jun 24;269(25):17160–17165. [PubMed] [Google Scholar]
  28. Tasaka K., Mio M., Okamoto M. The role of intracellular Ca2+ in the degranulation of skinned mast cells. Agents Actions. 1987 Apr;20(3-4):157–160. doi: 10.1007/BF02074656. [DOI] [PubMed] [Google Scholar]
  29. Tuominen H., Leino L., Akerman K. E. Does protein kinase C regulate receptor agonists-mediated elevation in the cytosolic Ca2+ in human neutrophils? Biochem Biophys Res Commun. 1994 Sep 15;203(2):998–1004. doi: 10.1006/bbrc.1994.2281. [DOI] [PubMed] [Google Scholar]
  30. Törnquist K., Tashjian A. H., Jr pH homeostasis in pituitary GH4C1 cells: basal intracellular pH is regulated by cytosolic free Ca2+ concentration. Endocrinology. 1992 Feb;130(2):717–725. doi: 10.1210/endo.130.2.1733720. [DOI] [PubMed] [Google Scholar]

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