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. 1993 Dec 1;296(Pt 2):481–488. doi: 10.1042/bj2960481

Activation of phosphatidylinositol 4,5-bisphosphate supply by agonists and non-hydrolysable GTP analogues.

L Stephens 1, T R Jackson 1, P T Hawkins 1
PMCID: PMC1137720  PMID: 8257441

Abstract

PtdIns(4,5)P2 serves as a precursor of a diverse family of signalling molecules, including diacylglycerol (and hence phosphatidic acid), Ins(1,4,5)P3 [and hence Ins(1,3,4,5)P4] and PtdIns(3,4,5)P3. The production of these messengers can be activated by agonists, and therefore the rate of utilization of PtdIns(4,5)P2 can vary dramatically. Although cells can only meet these large changes in demand for PtdIns(4,5)P2 by increasing its synthesis and/or by continuously cycling it at a rate that exceeds its potential consumption (avoiding the need for a co-ordinated activation mechanism), no satisfactory explanation for how this is achieved in agonist-stimulated cells has yet been provided. We show here that, in streptolysin-O-permeabilized neutrophils, N-formylmethionyl-leucyl-phenylalanine (FMLP), platelet-activating factor (PAF) and non-hydrolysable GTP analogues can cause large activations of PtdIns4P 5-kinase, suggesting that cells can accommodate agonist-activated rates of consumption of PtdIns(4,5)P2 without having to sustain continuous, comparably rapid and energetically expensive 'futile cycling' reactions.

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Selected References

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  1. Aub D. L., Putney J. W., Jr Metabolism of inositol phosphates in parotid cells: implications for the pathway of the phosphoinositide effect and for the possible messenger role of inositol trisphosphate. Life Sci. 1984 Apr 2;34(14):1347–1355. doi: 10.1016/0024-3205(84)90006-7. [DOI] [PubMed] [Google Scholar]
  2. Auger K. R., Serunian L. A., Soltoff S. P., Libby P., Cantley L. C. PDGF-dependent tyrosine phosphorylation stimulates production of novel polyphosphoinositides in intact cells. Cell. 1989 Apr 7;57(1):167–175. doi: 10.1016/0092-8674(89)90182-7. [DOI] [PubMed] [Google Scholar]
  3. BROCKERHOFF H., BALLOU C. E. On the metabolism of the brain phosphoinositide complex. J Biol Chem. 1962 Jun;237:1764–1766. [PubMed] [Google Scholar]
  4. Bazenet C. E., Ruano A. R., Brockman J. L., Anderson R. A. The human erythrocyte contains two forms of phosphatidylinositol-4-phosphate 5-kinase which are differentially active toward membranes. J Biol Chem. 1990 Oct 15;265(29):18012–18022. [PubMed] [Google Scholar]
  5. Benistant C., Thomas A. P., Rubin R. Effect of guanine nucleotides on polyphosphoinositide synthesis in rat liver plasma membranes. Biochem J. 1990 Nov 1;271(3):591–597. doi: 10.1042/bj2710591. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Billah M. M., Eckel S., Mullmann T. J., Egan R. W., Siegel M. I. Phosphatidylcholine hydrolysis by phospholipase D determines phosphatidate and diglyceride levels in chemotactic peptide-stimulated human neutrophils. Involvement of phosphatidate phosphohydrolase in signal transduction. J Biol Chem. 1989 Oct 15;264(29):17069–17077. [PubMed] [Google Scholar]
  7. Camps M., Hou C., Sidiropoulos D., Stock J. B., Jakobs K. H., Gierschik P. Stimulation of phospholipase C by guanine-nucleotide-binding protein beta gamma subunits. Eur J Biochem. 1992 Jun 15;206(3):821–831. doi: 10.1111/j.1432-1033.1992.tb16990.x. [DOI] [PubMed] [Google Scholar]
  8. Cantley L. C., Auger K. R., Carpenter C., Duckworth B., Graziani A., Kapeller R., Soltoff S. Oncogenes and signal transduction. Cell. 1991 Jan 25;64(2):281–302. doi: 10.1016/0092-8674(91)90639-g. [DOI] [PubMed] [Google Scholar]
  9. Carpenter C. L., Cantley L. C. Phosphoinositide kinases. Biochemistry. 1990 Dec 25;29(51):11147–11156. doi: 10.1021/bi00503a001. [DOI] [PubMed] [Google Scholar]
  10. Chahwala S. B., Fleischman L. F., Cantley L. Kinetic analysis of guanosine 5'-O-(3-thiotriphosphate) effects on phosphatidylinositol turnover in NRK cell homogenates. Biochemistry. 1987 Jan 27;26(2):612–622. doi: 10.1021/bi00376a037. [DOI] [PubMed] [Google Scholar]
  11. Cochet C., Filhol O., Payrastre B., Hunter T., Gill G. N. Interaction between the epidermal growth factor receptor and phosphoinositide kinases. J Biol Chem. 1991 Jan 5;266(1):637–644. [PubMed] [Google Scholar]
  12. Cockcroft S., Lamb J. R., Zanders E. D. Inositol lipid metabolism in human T lymphocytes activated via the T3 complex. Immunology. 1987 Feb;60(2):209–212. [PMC free article] [PubMed] [Google Scholar]
  13. Cockcroft S., Stutchfield J. G-proteins, the inositol lipid signalling pathway, and secretion. Philos Trans R Soc Lond B Biol Sci. 1988 Jul 26;320(1199):247–265. doi: 10.1098/rstb.1988.0075. [DOI] [PubMed] [Google Scholar]
  14. Corey S., Eguinoa A., Puyana-Theall K., Bolen J. B., Cantley L., Mollinedo F., Jackson T. R., Hawkins P. T., Stephens L. R. Granulocyte macrophage-colony stimulating factor stimulates both association and activation of phosphoinositide 3OH-kinase and src-related tyrosine kinase(s) in human myeloid derived cells. EMBO J. 1993 Jul;12(7):2681–2690. doi: 10.1002/j.1460-2075.1993.tb05929.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Creba J. A., Downes C. P., Hawkins P. T., Brewster G., Michell R. H., Kirk C. J. Rapid breakdown of phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate in rat hepatocytes stimulated by vasopressin and other Ca2+-mobilizing hormones. Biochem J. 1983 Jun 15;212(3):733–747. doi: 10.1042/bj2120733. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Dale G. L. Phosphatidylinositol 4-phosphate kinase is associated with the membrane skeleton in human erythrocytes. Biochem Biophys Res Commun. 1985 Nov 27;133(1):189–194. doi: 10.1016/0006-291x(85)91859-5. [DOI] [PubMed] [Google Scholar]
  17. Divecha N., Banfić H., Irvine R. F. The polyphosphoinositide cycle exists in the nuclei of Swiss 3T3 cells under the control of a receptor (for IGF-I) in the plasma membrane, and stimulation of the cycle increases nuclear diacylglycerol and apparently induces translocation of protein kinase C to the nucleus. EMBO J. 1991 Nov;10(11):3207–3214. doi: 10.1002/j.1460-2075.1991.tb04883.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Divecha N., Brooksbank C. E., Irvine R. F. Purification and characterization of phosphatidylinositol 4-phosphate 5-kinases. Biochem J. 1992 Dec 1;288(Pt 2):637–642. doi: 10.1042/bj2880637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Downes P., Michell R. H. Phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate: lipids in search of a function. Cell Calcium. 1982 Oct;3(4-5):467–502. doi: 10.1016/0143-4160(82)90031-8. [DOI] [PubMed] [Google Scholar]
  20. Fujita-Yamaguchi Y., Kathuria S. Characterization of receptor tyrosine-specific protein kinases by the use of inhibitors. Staurosporine is a 100-times more potent inhibitor of insulin receptor than IGF-I receptor. Biochem Biophys Res Commun. 1988 Dec 30;157(3):955–962. doi: 10.1016/s0006-291x(88)80967-7. [DOI] [PubMed] [Google Scholar]
  21. Halenda S. P., Feinstein M. B. Phorbol myristate acetate stimulates formation of phosphatidyl inositol 4-phosphate and phosphatidyl inositol 4,5-bisphosphate in human platelets. Biochem Biophys Res Commun. 1984 Oct 30;124(2):507–513. doi: 10.1016/0006-291x(84)91583-3. [DOI] [PubMed] [Google Scholar]
  22. Imai A., Gershengorn M. C. Phosphatidylinositol 4,5-bisphosphate turnover is transient while phosphatidylinositol turnover is persistent in thyrotropin-releasing hormone-stimulated rat pituitary cells. Proc Natl Acad Sci U S A. 1986 Nov;83(22):8540–8544. doi: 10.1073/pnas.83.22.8540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Inokuchi S., Imboden J. B. Antigen receptor-mediated regulation of sustained polyphosphoinositide turnover in a human T cell line. Evidence for a receptor-regulated pathway for production of phosphatidylinositol 4,5-bisphosphate. J Biol Chem. 1990 Apr 15;265(11):5983–5989. [PubMed] [Google Scholar]
  24. Irvine R. F. The enzymology of stimulated inositol lipid turnover. Cell Calcium. 1982 Oct;3(4-5):295–309. doi: 10.1016/0143-4160(82)90018-5. [DOI] [PubMed] [Google Scholar]
  25. King C. E., Hawkins P. T., Stephens L. R., Michell R. H. Determination of the steady-state turnover rates of the metabolically active pools of phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate in human erythrocytes. Biochem J. 1989 May 1;259(3):893–896. doi: 10.1042/bj2590893. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Lassing I., Lindberg U. Polyphosphoinositide synthesis in platelets stimulated with low concentrations of thrombin is enhanced before the activation of phospholipase C. FEBS Lett. 1990 Mar 26;262(2):231–233. doi: 10.1016/0014-5793(90)80197-q. [DOI] [PubMed] [Google Scholar]
  27. Ling L. E., Schulz J. T., Cantley L. C. Characterization and purification of membrane-associated phosphatidylinositol-4-phosphate kinase from human red blood cells. J Biol Chem. 1989 Mar 25;264(9):5080–5088. [PubMed] [Google Scholar]
  28. Moritz A., De Graan P. N., Gispen W. H., Wirtz K. W. Phosphatidic acid is a specific activator of phosphatidylinositol-4-phosphate kinase. J Biol Chem. 1992 Apr 15;267(11):7207–7210. [PubMed] [Google Scholar]
  29. Müller E., Hegewald H., Jaroszewicz K., Cumme G. A., Hoppe H., Frunder H. Turnover of phosphomonoester groups and compartmentation of polyphosphoinositides in human erythrocytes. Biochem J. 1986 May 1;235(3):775–783. doi: 10.1042/bj2350775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Nahas N., Plantavid M., Mauco G., Chap H. Association of phosphatidylinositol kinase and phosphatidylinositol 4-phosphate kinase activities with the cytoskeleton in human platelets. FEBS Lett. 1989 Mar 27;246(1-2):30–34. doi: 10.1016/0014-5793(89)80247-9. [DOI] [PubMed] [Google Scholar]
  31. Newsholme E. A., Crabtree B. Metabolic aspects of enzyme activity regulation. Symp Soc Exp Biol. 1973;27:429–460. [PubMed] [Google Scholar]
  32. Palmer S., Hawkins P. T., Michell R. H., Kirk C. J. The labelling of polyphosphoinositides with [32P]Pi and the accumulation of inositol phosphates in vasopressin-stimulated hepatocytes. Biochem J. 1986 Sep 1;238(2):491–499. doi: 10.1042/bj2380491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Pike L. J., Eakes A. T. Epidermal growth factor stimulates the production of phosphatidylinositol monophosphate and the breakdown of polyphosphoinositides in A431 cells. J Biol Chem. 1987 Feb 5;262(4):1644–1651. [PubMed] [Google Scholar]
  34. Pike M. C., Arndt C. Characterization of phosphatidylinositol and phosphatidylinositol-4-phosphate kinases in human neutrophils. J Immunol. 1988 Mar 15;140(6):1967–1973. [PubMed] [Google Scholar]
  35. Renard D., Poggioli J., Berthon B., Claret M. How far does phospholipase C activity depend on the cell calcium concentration? A study in intact cells. Biochem J. 1987 Apr 15;243(2):391–398. doi: 10.1042/bj2430391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Rhee S. G., Choi K. D. Regulation of inositol phospholipid-specific phospholipase C isozymes. J Biol Chem. 1992 Jun 25;267(18):12393–12396. [PubMed] [Google Scholar]
  37. Shears S. B. Regulation of the metabolism of 1,2-diacylglycerols and inositol phosphates that respond to receptor activation. Pharmacol Ther. 1991;49(1-2):79–104. doi: 10.1016/0163-7258(91)90023-f. [DOI] [PubMed] [Google Scholar]
  38. Smith C. D., Chang K. J. Regulation of brain phosphatidylinositol-4-phosphate kinase by GTP analogues. A potential role for guanine nucleotide regulatory proteins. J Biol Chem. 1989 Feb 25;264(6):3206–3210. [PubMed] [Google Scholar]
  39. Stephens L. R., Berrie C. P., Irvine R. F. Agonist-stimulated inositol phosphate metabolism in avian erythrocytes. Biochem J. 1990 Jul 1;269(1):65–72. doi: 10.1042/bj2690065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Stephens L. R., Downes C. P. Product-precursor relationships amongst inositol polyphosphates. Incorporation of [32P]Pi into myo-inositol 1,3,4,6-tetrakisphosphate, myo-inositol 1,3,4,5-tetrakisphosphate, myo-inositol 3,4,5,6-tetrakisphosphate and myo-inositol 1,3,4,5,6-pentakisphosphate in intact avian erythrocytes. Biochem J. 1990 Jan 15;265(2):435–452. doi: 10.1042/bj2650435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Stephens L. R., Hughes K. T., Irvine R. F. Pathway of phosphatidylinositol(3,4,5)-trisphosphate synthesis in activated neutrophils. Nature. 1991 May 2;351(6321):33–39. doi: 10.1038/351033a0. [DOI] [PubMed] [Google Scholar]
  42. Stephens L., Jackson T., Hawkins P. T. Synthesis of phosphatidylinositol 3,4,5-trisphosphate in permeabilized neutrophils regulated by receptors and G-proteins. J Biol Chem. 1993 Aug 15;268(23):17162–17172. [PubMed] [Google Scholar]
  43. Taylor M. V., Metcalfe J. C., Hesketh T. R., Smith G. A., Moore J. P. Mitogens increase phosphorylation of phosphoinositides in thymocytes. 1984 Nov 29-Dec 5Nature. 312(5993):462–465. doi: 10.1038/312462a0. [DOI] [PubMed] [Google Scholar]
  44. Thomas A. P., Marks J. S., Coll K. E., Williamson J. R. Quantitation and early kinetics of inositol lipid changes induced by vasopressin in isolated and cultured hepatocytes. J Biol Chem. 1983 May 10;258(9):5716–5725. [PubMed] [Google Scholar]
  45. Traynor-Kaplan A. E., Thompson B. L., Harris A. L., Taylor P., Omann G. M., Sklar L. A. Transient increase in phosphatidylinositol 3,4-bisphosphate and phosphatidylinositol trisphosphate during activation of human neutrophils. J Biol Chem. 1989 Sep 15;264(26):15668–15673. [PubMed] [Google Scholar]
  46. Urumow T., Wieland O. H. Purification and partial characterization of phosphatidylinositol-4-phosphate kinase from rat liver plasma membranes. Further evidence for a stimulatory G-protein. Biochim Biophys Acta. 1990 Apr 9;1052(1):152–158. doi: 10.1016/0167-4889(90)90070-t. [DOI] [PubMed] [Google Scholar]
  47. Wilson D. B., Neufeld E. J., Majerus P. W. Phosphoinositide interconversion in thrombin-stimulated human platelets. J Biol Chem. 1985 Jan 25;260(2):1046–1051. [PubMed] [Google Scholar]
  48. von zur Mühlen F., Eckstein F., Penner R. Guanosine 5'-[beta-thio]triphosphate selectively activates calcium signaling in mast cells. Proc Natl Acad Sci U S A. 1991 Feb 1;88(3):926–930. doi: 10.1073/pnas.88.3.926. [DOI] [PMC free article] [PubMed] [Google Scholar]

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