Effects of lysophosphatidylcholine and arachidonic acid on the regulation of intracellular Ca2+ transport

  • I. Rustenbeck
  • S. Lenzen
Article

Summary

The role of lysophosphatidylcholine and arachidonic acid in signal transduction was investigated using subcellular organelles and permeabilized cells from liver. Both substances can be generated intracellularly by the action of phospholipase A2 on phosphatidy1choline. Lysophosphatidylcholine as well as arachidonic acid raised the free Ca2+ concentration in the incubation media of permeabilized cells, isolated mitochondria and microsomes. The half maximally effective concentrations for Ca2+ release from mitochondria were 78 ± 1 μmol/l for lysophosphatidylcholine and 80 ± 11 μmol/l for arachidonic acid. Though isolated microsomes released Ca2+ in response to both agents, the combined presence of mitochondria and microsomes did not exhibit a synergism in Ca2+ release in response to arachidonic acid; the increase in the free Ca2+ concentration in response to lysophosphatidylcholine was even smaller than with mitochondria alone. It is concluded that the two reaction products of phospholipase A2 can raise the cytoplasmic Ca2+ concentration and therefore may participate in cellular signal transduction.

Key words

Lysophosphatidylcholine Arachidonic acid Phospholipase A2 Ca2+ Transport Permeabilized hepatocytes Mitochondria Microsomes 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Becker GL, Fiskum G, Lehninger A (1980) Regulation of free calcium by liver mitochondria and endoplasmic reticulum. J Biol Chem 255:9009–9012Google Scholar
  2. Berridge MJ, Irvine RF (1984) Inositol trisphosphate, a novel second messenger in cellular signal transduction. Nature 312:315–321Google Scholar
  3. Brenner RR (1984) Effect of unsaturated acids on membrane structure and enzyme kinetics. Prog Lipid Res 23:69–96Google Scholar
  4. Burgoyne RD, Cheek TR, O'Sullivan A (1987) Receptor-activation of phospholipase A2 in cellular signalling. Trends Biochem Sci 12:332–333Google Scholar
  5. Carafoli E (1987) Intracellular calcium homeostasis. Annu Rev Biochem 56:395–433Google Scholar
  6. Chang J, Musser JH, McGregor H (1987) Phospholipase A2: function and pharmacological regulation. Biochem Pharmacol 36:2429–2436Google Scholar
  7. Cheah AM (1981) Effect of long chain unsaturated fatty acids on the calcium transport of sarcoplasmic reticulum. Biochim Biophys Acta 648:113–119Google Scholar
  8. Dennis EA (1987) Phospholipase A2 mechanisms: inhibition and role in arachidonic acid release. Drug Dev Res 10:205–220Google Scholar
  9. Garcia-Gil M, Siraganian PR (1986) Phospholipase A2 stimulation during cell secretion in rat basophilic leukemia cells. J Immunol 136:259–263Google Scholar
  10. Igbavboa U, Pfeiffer DR (1988) EGTA inhibits reverse uniport-dependent Ca2+ release from uncoupled mitochondria. J Biol Chem 263:1405–1412Google Scholar
  11. Jeffcoat R, James AT (1984) The regulation of desaturation and elongation of fatty acids in mammals. In: Numa S (ed) Fatty acid metabolism and its regulation. Elsevier Biomedical, Amsterdam, pp 85–112Google Scholar
  12. Jelsema CL (1987) Light activation of phospholipase A2 in rod outer segments of bovine retina and its modulation by GTP-binding proteins. J Biol Chem 262:163–168Google Scholar
  13. Lenzen S, Panten U (1985) A versatile Ca2+ ion-sensitive minielectrode with a microincubation chamber. Anal Biochem 149:301–308Google Scholar
  14. Lenzen S, Schmidt W, Panten U (1985) Transamination of neutral amino acids and α-keto acids in pancreatic B-cell mitochondria. J Biol Chem 260:12629–12634Google Scholar
  15. Lenzen S, Hickethier R, Panten U (1986) Interactions between spermine and Mg2+ on mitochondrial Ca2+ transport. J Biol Chem 261:16478–16483Google Scholar
  16. McKnight GS (1977) A colorimetric method for the determination of submicrogram quantities of protein. Anal Biochem 78: 86–92Google Scholar
  17. Needleman P, Turk J, Jakschik BA, Morrison AR, Lelkowith JB (1986) Arachidonic acid metabolism. Annu Rev Biochem 55:69–102Google Scholar
  18. Nicchitta CV, Williamson JR (1984) Spermine; a regulator of mitochondrial calcium cycling. J Biol Chem 259:12978–12983Google Scholar
  19. Okayasu T, Hasegawa K, Ishibashi T (1987) Platelet-activating factor stimulates metabolism of phosphoinositides via phospholipase A2 in primary cultured rat hepatocytes. J Lipid Res 28:760–767Google Scholar
  20. Probst I, Unthan-Fechner K (1985) Activation of glycolysis by insulin with a sequential increase of the 6-phosphofructo-2-kinase activity, fructose-2,6-bisphosphate level and pyruvate kinase activity in cultured rat hepatocytes. Eur J Biochem 153:347–353Google Scholar
  21. Roman I, Gmai P, Nowicka C, Angielski S (1979) Regulation of Ca2+ efflux from kidney and liver mitochondria by unsaturated fatty acids and Na+ ions. Eur J Biochem 102:615–623Google Scholar
  22. Rottenberg H, Hashimoto K (1986) Fatty acid uncoupling of oxidative phosphorylation in rat liver mitochondria. Biochemistry 25:1747–1755Google Scholar
  23. Seglen PO (1973) Preparation of rat liver cells. 3. Enzymatic requirements for tissue dispersion. Exp Cell Res 82:391–398Google Scholar
  24. Slotboom AJ, Verheij HM, De Haas GH (1982) On the mechanism of phospholipase A2. In: Hawthorne JN, Ansell GB (eds) Phospholipids. Elsevier Biomedical, Amsterdam, pp 359–434Google Scholar
  25. Whiting JA, Barritt GJ (1982) On the mechanism by which hormones induce the release of Ca2+ from mitochondria in the liver cell. Biochem J 206:121–129Google Scholar
  26. Wolf BA, Turk J, Sherman WR, McDaniel ML (1986) Intracellular Ca2+ mobilization by arachidonic acid. J Biol Chem 261: 3501–3511Google Scholar

Copyright information

© Springer-Verlag 1989

Authors and Affiliations

  • I. Rustenbeck
    • 1
  • S. Lenzen
    • 1
  1. 1.Institute of Pharmacology and ToxicologyUnversity of GöttingenGöttingenFederal Republic of Germany

Personalised recommendations