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. 1992 Dec 1;288(Pt 2):357–360. doi: 10.1042/bj2880357

Oscillations of cytosolic free calcium concentration in the presence of intracellular antibodies to phosphatidylinositol 4,5-bisphosphate in voltage-clamped guinea-pig hepatocytes.

J Noel 1, K Fukami 1, A M Hill 1, T Capiod 1
PMCID: PMC1132019  PMID: 1334405

Abstract

In liver cells, the stimulation of alpha 1-adrenoceptors by noradrenaline induces the production of Ins(1,4,5)P3 through the degradation of membrane polyphosphoinositides [PtdIns(4,5)P2]. InsP3 evokes in turn the release of Ca2+ from internal stores. Our results show that the internal perfusion of single guinea-pig hepatocytes with monoclonal anti-PtdInsP2 antibody blocks the rise in cytosolic free Ca2+ concn. ([Ca2+]i) evoked by noradrenaline, an InsP3-dependent agonist, but not by the monohydroxylated bile acid taurolithocholate 3-sulphate, which is known to permeabilize the endoplasmic reticulum. In these conditions, the bile acid elicited either fast or slow fluctuations of [Ca2+]i independently of any InsP3 production. The responses to the bile acid were also observed in the absence of external Ca2+. The presence of intracellular anti-PtdInsP2 antibody does not affect the response to a photolytic release of InsP3 (1.5 microM final concn.) from a caged precursor.

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Selected References

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  1. Augert G., Blackmore P. F., Exton J. H. Changes in the concentration and fatty acid composition of phosphoinositides induced by hormones in hepatocytes. J Biol Chem. 1989 Feb 15;264(5):2574–2580. [PubMed] [Google Scholar]
  2. Berridge M. J. Cytoplasmic calcium oscillations: a two pool model. Cell Calcium. 1991 Feb-Mar;12(2-3):63–72. doi: 10.1016/0143-4160(91)90009-4. [DOI] [PubMed] [Google Scholar]
  3. Bezprozvanny I., Watras J., Ehrlich B. E. Bell-shaped calcium-response curves of Ins(1,4,5)P3- and calcium-gated channels from endoplasmic reticulum of cerebellum. Nature. 1991 Jun 27;351(6329):751–754. doi: 10.1038/351751a0. [DOI] [PubMed] [Google Scholar]
  4. Capiod T., Combettes L., Noel J., Claret M. Evidence for bile acid-evoked oscillations of Ca2(+)-dependent K+ permeability unrelated to a D-myo-inositol 1,4,5-trisphosphate effect in isolated guinea pig liver cells. J Biol Chem. 1991 Jan 5;266(1):268–273. [PubMed] [Google Scholar]
  5. Capiod T., Ogden D. C. Properties of membrane ion conductances evoked by hormonal stimulation of guinea-pig and rabbit isolated hepatocytes. Proc R Soc Lond B Biol Sci. 1989 Mar 22;236(1283):187–201. doi: 10.1098/rspb.1989.0020. [DOI] [PubMed] [Google Scholar]
  6. Capiod T., Ogden D. C. The properties of calcium-activated potassium ion channels in guinea-pig isolated hepatocytes. J Physiol. 1989 Feb;409:285–295. doi: 10.1113/jphysiol.1989.sp017497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Combettes L., Berthon B., Doucet E., Erlinger S., Claret M. Bile acids mobilise internal Ca2+ independently of external Ca2+ in rat hepatocytes. Eur J Biochem. 1990 Jul 5;190(3):619–623. doi: 10.1111/j.1432-1033.1990.tb15617.x. [DOI] [PubMed] [Google Scholar]
  8. Combettes L., Berthon B., Doucet E., Erlinger S., Claret M. Characteristics of bile acid-mediated Ca2+ release from permeabilized liver cells and liver microsomes. J Biol Chem. 1989 Jan 5;264(1):157–167. [PubMed] [Google Scholar]
  9. Combettes L., Dumont M., Berthon B., Erlinger S., Claret M. Release of calcium from the endoplasmic reticulum by bile acids in rat liver cells. J Biol Chem. 1988 Feb 15;263(5):2299–2303. [PubMed] [Google Scholar]
  10. Dasso L. L., Taylor C. W. Heparin and other polyanions uncouple alpha 1-adrenoceptors from G-proteins. Biochem J. 1991 Dec 15;280(Pt 3):791–795. doi: 10.1042/bj2800791. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ey P. L., Prowse S. J., Jenkin C. R. Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-sepharose. Immunochemistry. 1978 Jul;15(7):429–436. doi: 10.1016/0161-5890(78)90070-6. [DOI] [PubMed] [Google Scholar]
  12. Field A. C., Jenkinson D. H. The effect of noradrenaline on the ion permeability of isolated mammalian hepatocytes, studied by intracellular recording. J Physiol. 1987 Nov;392:493–512. doi: 10.1113/jphysiol.1987.sp016793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Finch E. A., Turner T. J., Goldin S. M. Calcium as a coagonist of inositol 1,4,5-trisphosphate-induced calcium release. Science. 1991 Apr 19;252(5004):443–446. doi: 10.1126/science.2017683. [DOI] [PubMed] [Google Scholar]
  14. Fukami K., Matsuoka K., Nakanishi O., Yamakawa A., Kawai S., Takenawa T. Antibody to phosphatidylinositol 4,5-bisphosphate inhibits oncogene-induced mitogenesis. Proc Natl Acad Sci U S A. 1988 Dec;85(23):9057–9061. doi: 10.1073/pnas.85.23.9057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Huang C. L., Takenawa T., Ives H. E. Platelet-derived growth factor-mediated Ca2+ entry is blocked by antibodies to phosphatidylinositol 4,5-bisphosphate but does not involve heparin-sensitive inositol 1,4,5-trisphosphate receptors. J Biol Chem. 1991 Mar 5;266(7):4045–4048. [PubMed] [Google Scholar]
  16. Krause K. H. Ca(2+)-storage organelles. FEBS Lett. 1991 Jul 22;285(2):225–229. doi: 10.1016/0014-5793(91)80806-e. [DOI] [PubMed] [Google Scholar]
  17. Matuoka K., Fukami K., Nakanishi O., Kawai S., Takenawa T. Mitogenesis in response to PDGF and bombesin abolished by microinjection of antibody to PIP2. Science. 1988 Feb 5;239(4840):640–643. doi: 10.1126/science.2829356. [DOI] [PubMed] [Google Scholar]
  18. Missiaen L., Taylor C. W., Berridge M. J. Spontaneous calcium release from inositol trisphosphate-sensitive calcium stores. Nature. 1991 Jul 18;352(6332):241–244. doi: 10.1038/352241a0. [DOI] [PubMed] [Google Scholar]
  19. Ogden D. C., Capiod T., Walker J. W., Trentham D. R. Kinetics of the conductance evoked by noradrenaline, inositol trisphosphate or Ca2+ in guinea-pig isolated hepatocytes. J Physiol. 1990 Mar;422:585–602. doi: 10.1113/jphysiol.1990.sp018002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Oldershaw K. A., Taylor C. W. 2,5-Di-(tert-butyl)-1,4-benzohydroquinone mobilizes inositol 1,4,5-trisphosphate-sensitive and -insensitive Ca2+ stores. FEBS Lett. 1990 Nov 12;274(1-2):214–216. doi: 10.1016/0014-5793(90)81366-v. [DOI] [PubMed] [Google Scholar]
  21. Pusch M., Neher E. Rates of diffusional exchange between small cells and a measuring patch pipette. Pflugers Arch. 1988 Feb;411(2):204–211. doi: 10.1007/BF00582316. [DOI] [PubMed] [Google Scholar]
  22. Rapp G., Güth K. A low cost high intensity flash device for photolysis experiments. Pflugers Arch. 1988 Feb;411(2):200–203. doi: 10.1007/BF00582315. [DOI] [PubMed] [Google Scholar]
  23. Rooney T. A., Sass E. J., Thomas A. P. Characterization of cytosolic calcium oscillations induced by phenylephrine and vasopressin in single fura-2-loaded hepatocytes. J Biol Chem. 1989 Oct 15;264(29):17131–17141. [PubMed] [Google Scholar]
  24. Shoshan-Barmatz V., Zhang G. H., Garretson L., Kraus-Friedmann N. Distinct ryanodine- and inositol 1,4,5-trisphosphate-binding sites in hepatic microsomes. Biochem J. 1990 Jun 15;268(3):699–705. doi: 10.1042/bj2680699. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Volpe P., Villa A., Damiani E., Sharp A. H., Podini P., Snyder S. H., Meldolesi J. Heterogeneity of microsomal Ca2+ stores in chicken Purkinje neurons. EMBO J. 1991 Nov;10(11):3183–3189. doi: 10.1002/j.1460-2075.1991.tb04880.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Walker J. W., Feeney J., Trentham D. R. Photolabile precursors of inositol phosphates. Preparation and properties of 1-(2-nitrophenyl)ethyl esters of myo-inositol 1,4,5-trisphosphate. Biochemistry. 1989 Apr 18;28(8):3272–3280. doi: 10.1021/bi00434a023. [DOI] [PubMed] [Google Scholar]
  27. Woods N. M., Cuthbertson K. S., Cobbold P. H. Repetitive transient rises in cytoplasmic free calcium in hormone-stimulated hepatocytes. Nature. 1986 Feb 13;319(6054):600–602. doi: 10.1038/319600a0. [DOI] [PubMed] [Google Scholar]

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