The regulation and cellular functions of phosphatidylcholine hydrolysis (original) (raw)

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Selected References

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  1. Abdel-Latif A. A. Calcium-mobilizing receptors, polyphosphoinositides, and the generation of second messengers. Pharmacol Rev. 1986 Sep;38(3):227–272. [PubMed] [Google Scholar]
  2. Agwu D. E., McPhail L. C., Chabot M. C., Daniel L. W., Wykle R. L., McCall C. E. Choline-linked phosphoglycerides. A source of phosphatidic acid and diglycerides in stimulated neutrophils. J Biol Chem. 1989 Jan 25;264(3):1405–1413. [PubMed] [Google Scholar]
  3. Agwu D. E., McPhail L. C., Wykle R. L., McCall C. E. Mass determination of receptor-mediated accumulation of phosphatidate and diglycerides in human neutrophils measured by Coomassie blue staining and densitometry. Biochem Biophys Res Commun. 1989 Feb 28;159(1):79–86. doi: 10.1016/0006-291x(89)92407-8. [DOI] [PubMed] [Google Scholar]
  4. Alling C., Gustavsson L., Anggård E. An abnormal phospholipid in rat organs after ethanol treatment. FEBS Lett. 1983 Feb 7;152(1):24–28. doi: 10.1016/0014-5793(83)80474-8. [DOI] [PubMed] [Google Scholar]
  5. Anthes J. C., Eckel S., Siegel M. I., Egan R. W., Billah M. M. Phospholipase D in homogenates from HL-60 granulocytes: implications of calcium and G protein control. Biochem Biophys Res Commun. 1989 Aug 30;163(1):657–664. doi: 10.1016/0006-291x(89)92187-6. [DOI] [PubMed] [Google Scholar]
  6. Arthur G., Mock T., Zaborniak C., Choy P. C. The distribution and acyl composition of plasmalogens in guinea pig heart. Lipids. 1985 Oct;20(10):693–698. doi: 10.1007/BF02534389. [DOI] [PubMed] [Google Scholar]
  7. Asaoka Y., Kikkawa U., Sekiguchi K., Shearman M. S., Kosaka Y., Nakano Y., Satoh T., Nishizuka Y. Activation of a brain-specific protein kinase C subspecies in the presence of phosphatidylethanol. FEBS Lett. 1988 Apr 11;231(1):221–224. doi: 10.1016/0014-5793(88)80735-x. [DOI] [PubMed] [Google Scholar]
  8. Balsinde J., Diez E., Mollinedo F. Phosphatidylinositol-specific phospholipase D: a pathway for generation of a second messenger. Biochem Biophys Res Commun. 1988 Jul 29;154(2):502–508. doi: 10.1016/0006-291x(88)90168-4. [DOI] [PubMed] [Google Scholar]
  9. Berridge M. J. Inositol trisphosphate and diacylglycerol as second messengers. Biochem J. 1984 Jun 1;220(2):345–360. doi: 10.1042/bj2200345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Berridge M. J., Irvine R. F. Inositol phosphates and cell signalling. Nature. 1989 Sep 21;341(6239):197–205. doi: 10.1038/341197a0. [DOI] [PubMed] [Google Scholar]
  11. Besterman J. M., Duronio V., Cuatrecasas P. Rapid formation of diacylglycerol from phosphatidylcholine: a pathway for generation of a second messenger. Proc Natl Acad Sci U S A. 1986 Sep;83(18):6785–6789. doi: 10.1073/pnas.83.18.6785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Besterman J. M., Pollenz R. S., Booker E. L., Jr, Cuatrecasas P. Diacylglycerol-induced translocation of diacylglycerol kinase: use of affinity-purified enzyme in a reconstitution system. Proc Natl Acad Sci U S A. 1986 Dec;83(24):9378–9382. doi: 10.1073/pnas.83.24.9378. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. 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]
  14. Billah M. M., Pai J. K., Mullmann T. J., Egan R. W., Siegel M. I. Regulation of phospholipase D in HL-60 granulocytes. Activation by phorbol esters, diglyceride, and calcium ionophore via protein kinase- independent mechanisms. J Biol Chem. 1989 May 25;264(15):9069–9076. [PubMed] [Google Scholar]
  15. Bishop W. R., Ganong B. R., Bell R. M. Attenuation of sn-1,2-diacylglycerol second messengers by diacylglycerol kinase. Inhibition by diacylglycerol analogs in vitro and in human platelets. J Biol Chem. 1986 May 25;261(15):6993–7000. [PubMed] [Google Scholar]
  16. Blusztajn J. K., Liscovitch M., Mauron C., Richardson U. I., Wurtman R. J. Phosphatidylcholine as a precursor of choline for acetylcholine synthesis. J Neural Transm Suppl. 1987;24:247–259. [PubMed] [Google Scholar]
  17. Bocckino S. B., Blackmore P. F., Exton J. H. Stimulation of 1,2-diacylglycerol accumulation in hepatocytes by vasopressin, epinephrine, and angiotensin II. J Biol Chem. 1985 Nov 15;260(26):14201–14207. [PubMed] [Google Scholar]
  18. Bocckino S. B., Blackmore P. F., Wilson P. B., Exton J. H. Phosphatidate accumulation in hormone-treated hepatocytes via a phospholipase D mechanism. J Biol Chem. 1987 Nov 5;262(31):15309–15315. [PubMed] [Google Scholar]
  19. Bocckino S. B., Wilson P. B., Exton J. H. Ca2+-mobilizing hormones elicit phosphatidylethanol accumulation via phospholipase D activation. FEBS Lett. 1987 Dec 10;225(1-2):201–204. doi: 10.1016/0014-5793(87)81157-2. [DOI] [PubMed] [Google Scholar]
  20. Brindley D. N. Intracellular translocation of phosphatidate phosphohydrolase and its possible role in the control of glycerolipid synthesis. Prog Lipid Res. 1984;23(3):115–133. doi: 10.1016/0163-7827(84)90001-8. [DOI] [PubMed] [Google Scholar]
  21. Cabot M. C., Welsh C. J., Cao H. T., Chabbott H. The phosphatidylcholine pathway of diacylglycerol formation stimulated by phorbol diesters occurs via phospholipase D activation. FEBS Lett. 1988 Jun 6;233(1):153–157. doi: 10.1016/0014-5793(88)81374-7. [DOI] [PubMed] [Google Scholar]
  22. Cabot M. C., Welsh C. J., Zhang Z. C., Cao H. T., Chabbott H., Lebowitz M. Vasopressin, phorbol diesters and serum elicit choline glycerophospholipid hydrolysis and diacylglycerol formation in nontransformed cells: transformed derivatives do not respond. Biochim Biophys Acta. 1988 Mar 4;959(1):46–57. doi: 10.1016/0005-2760(88)90148-8. [DOI] [PubMed] [Google Scholar]
  23. Cabot M. C., Welsh C. J., Zhang Z. C., Cao H. T. Evidence for a protein kinase C-directed mechanism in the phorbol diester-induced phospholipase D pathway of diacylglycerol generation from phosphatidylcholine. FEBS Lett. 1989 Mar 13;245(1-2):85–90. doi: 10.1016/0014-5793(89)80197-8. [DOI] [PubMed] [Google Scholar]
  24. Chalifour R. J., Kanfer J. N. Microsomal phospholipase D of rat brain and lung tissues. Biochem Biophys Res Commun. 1980 Sep 30;96(2):742–747. doi: 10.1016/0006-291x(80)91417-5. [DOI] [PubMed] [Google Scholar]
  25. Chalifour R., Kanfer J. N. Fatty acid activation and temperature perturbation of rat brain microsomal phospholipase D. J Neurochem. 1982 Aug;39(2):299–305. doi: 10.1111/j.1471-4159.1982.tb03946.x. [DOI] [PubMed] [Google Scholar]
  26. Clark M. A., Littlejohn D., Conway T. M., Mong S., Steiner S., Crooke S. T. Leukotriene D4 treatment of bovine aortic endothelial cells and murine smooth muscle cells in culture results in an increase in phospholipase A2 activity. J Biol Chem. 1986 Aug 15;261(23):10713–10718. [PubMed] [Google Scholar]
  27. Clark M. A., Shorr R. G., Bomalaski J. S. Antibodies prepared to Bacillus cereus phospholipase C crossreact with a phosphatidylcholine preferring phospholipase C in mammalian cells. Biochem Biophys Res Commun. 1986 Oct 15;140(1):114–119. doi: 10.1016/0006-291x(86)91065-x. [DOI] [PubMed] [Google Scholar]
  28. Clarke N. G., Irvine R. F., Dawson R. M. Formation of bis(phosphatidyl)inositol and phosphatidic acid by phospholipase D action on phosphatidylinositol. Biochem J. 1981 May 1;195(2):521–523. doi: 10.1042/bj1950521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Cockcroft S., Allan D. The fatty acid composition of phosphatidylinositol, phosphatidate and 1,2-diacylglycerol in stimulated human neutrophils. Biochem J. 1984 Sep 1;222(2):557–559. doi: 10.1042/bj2220557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Cockcroft S. Ca2+-dependent conversion of phosphatidylinositol to phosphatidate in neutrophils stimulated with fMet-Leu-Phe or ionophore A23187. Biochim Biophys Acta. 1984 Aug 15;795(1):37–46. doi: 10.1016/0005-2760(84)90102-4. [DOI] [PubMed] [Google Scholar]
  31. Corradetti R., Lindmar R., Löffelholz K. Mobilization of cellular choline by stimulation of muscarine receptors in isolated chicken heart and rat cortex in vivo. J Pharmacol Exp Ther. 1983 Sep;226(3):826–832. [PubMed] [Google Scholar]
  32. Daniel L. W., Small G. W., Schmitt J. D., Marasco C. J., Ishaq K., Piantadosi C. Alkyl-linked diglycerides inhibit protein kinase C activation by diacylglycerols. Biochem Biophys Res Commun. 1988 Feb 29;151(1):291–297. doi: 10.1016/0006-291x(88)90592-x. [DOI] [PubMed] [Google Scholar]
  33. Daniel L. W., Waite M., Wykle R. L. A novel mechanism of diglyceride formation. 12-O-tetradecanoylphorbol-13-acetate stimulates the cyclic breakdown and resynthesis of phosphatidylcholine. J Biol Chem. 1986 Jul 15;261(20):9128–9132. [PubMed] [Google Scholar]
  34. Dawson R. M. The formation of phosphatidylglycerol and other phospholipids by the transferase activity of phospholipase D. Biochem J. 1967 Jan;102(1):205–210. doi: 10.1042/bj1020205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Domino S. E., Bocckino S. B., Garbers D. L. Activation of phospholipase D by the fucose-sulfate glycoconjugate that induces an acrosome reaction in spermatozoa. J Biol Chem. 1989 Jun 5;264(16):9412–9419. [PubMed] [Google Scholar]
  36. Dunlop M., Metz S. A. A phospholipase D-like mechanism in pancreatic islet cells: stimulation by calcium ionophore, phorbol ester and sodium fluoride. Biochem Biophys Res Commun. 1989 Sep 15;163(2):922–928. doi: 10.1016/0006-291x(89)92310-3. [DOI] [PubMed] [Google Scholar]
  37. Duronio V., Nip L., Pelech S. L. Interleukin 3 stimulates phosphatidylcholine turnover in a mast/megakaryocyte cell line. Biochem Biophys Res Commun. 1989 Oct 31;164(2):804–808. doi: 10.1016/0006-291x(89)91530-1. [DOI] [PubMed] [Google Scholar]
  38. Edgar A. D., Freysz L. Phospholipase activities of rat brain cytosol. Occurrence of phospholipase C activity with phosphatidylcholine. Biochim Biophys Acta. 1982 May 13;711(2):224–228. doi: 10.1016/0005-2760(82)90030-3. [DOI] [PubMed] [Google Scholar]
  39. Exton J. H. Mechanisms of action of calcium-mobilizing agonists: some variations on a young theme. FASEB J. 1988 Aug;2(11):2670–2676. doi: 10.1096/fasebj.2.11.2456243. [DOI] [PubMed] [Google Scholar]
  40. Farese R. V. Calcium as an intracellular mediator of hormone action: intracellular phospholipid signaling systems. Am J Med Sci. 1988 Oct;296(4):223–230. [PubMed] [Google Scholar]
  41. Ford D. A., Miyake R., Glaser P. E., Gross R. W. Activation of protein kinase C by naturally occurring ether-linked diglycerides. J Biol Chem. 1989 Aug 15;264(23):13818–13824. [PubMed] [Google Scholar]
  42. Fukami K., Takenawa T. Quantitative changes in polyphosphoinositides 1,2-diacylglycerol and inositol 1,4,5-trisphosphate by platelet-derived growth factor and prostaglandin F2 alpha. J Biol Chem. 1989 Sep 5;264(25):14985–14989. [PubMed] [Google Scholar]
  43. Ganong B. R., Loomis C. R., Hannun Y. A., Bell R. M. Specificity and mechanism of protein kinase C activation by sn-1,2-diacylglycerols. Proc Natl Acad Sci U S A. 1986 Mar;83(5):1184–1188. doi: 10.1073/pnas.83.5.1184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Gelas P., Ribbes G., Record M., Terce F., Chap H. Differential activation by fMet-Leu-Phe and phorbol ester of a plasma membrane phosphatidylcholine-specific phospholipase D in human neutrophil. FEBS Lett. 1989 Jul 17;251(1-2):213–218. doi: 10.1016/0014-5793(89)81457-7. [DOI] [PubMed] [Google Scholar]
  45. Griendling K. K., Rittenhouse S. E., Brock T. A., Ekstein L. S., Gimbrone M. A., Jr, Alexander R. W. Sustained diacylglycerol formation from inositol phospholipids in angiotensin II-stimulated vascular smooth muscle cells. J Biol Chem. 1986 May 5;261(13):5901–5906. [PubMed] [Google Scholar]
  46. Grillone L. R., Clark M. A., Godfrey R. W., Stassen F., Crooke S. T. Vasopressin induces V1 receptors to activate phosphatidylinositol- and phosphatidylcholine-specific phospholipase C and stimulates the release of arachidonic acid by at least two pathways in the smooth muscle cell line, A-10. J Biol Chem. 1988 Feb 25;263(6):2658–2663. [PubMed] [Google Scholar]
  47. Grove R. I., Schimmel S. D. Effects of 12-O-tetradecanoylphorbol 13-acetate on glycerolipid metabolism in cultured myoblasts. Biochim Biophys Acta. 1982 May 13;711(2):272–280. doi: 10.1016/0005-2760(82)90036-4. [DOI] [PubMed] [Google Scholar]
  48. Guy G. R., Murray A. W. Tumor promoter stimulation of phosphatidylcholine turnover in HeLa cells. Cancer Res. 1982 May;42(5):1980–1985. [PubMed] [Google Scholar]
  49. Haagsman H. P., de Haas C. G., Geelen M. J., van Golde L. M. Regulation of triacylglycerol synthesis in the liver. Modulation of diacylglycerol acyltransferase activity in vitro. J Biol Chem. 1982 Sep 25;257(18):10593–10598. [PubMed] [Google Scholar]
  50. Hanahan D. J. Platelet activating factor: a biologically active phosphoglyceride. Annu Rev Biochem. 1986;55:483–509. doi: 10.1146/annurev.bi.55.070186.002411. [DOI] [PubMed] [Google Scholar]
  51. Hattori H., Kanfer J. N. Synaptosomal phospholipase D potential role in providing choline for acetylcholine synthesis. J Neurochem. 1985 Nov;45(5):1578–1584. doi: 10.1111/j.1471-4159.1985.tb07229.x. [DOI] [PubMed] [Google Scholar]
  52. Heller M. Phospholipase D. Adv Lipid Res. 1978;16:267–326. doi: 10.1016/b978-0-12-024916-9.50011-1. [DOI] [PubMed] [Google Scholar]
  53. Holmes R. P., Yoss N. L. Failure of phosphatidic acid to translocate Ca2+ across phosphatidylcholine membranes. Nature. 1983 Oct 13;305(5935):637–638. doi: 10.1038/305637a0. [DOI] [PubMed] [Google Scholar]
  54. Holmsen H., Dangelmaier C. A., Rongved S. Tight coupling of thrombin-induced acid hydrolase secretion and phosphatidate synthesis to receptor occupancy in human platelets. Biochem J. 1984 Aug 15;222(1):157–167. doi: 10.1042/bj2220157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Horn W., Karnovsky M. L. Features of the translocation of protein kinase C in neutrophils stimulated with the chemotactic peptide f-Met-Leu-Phe. Biochem Biophys Res Commun. 1986 Sep 30;139(3):1169–1175. doi: 10.1016/s0006-291x(86)80300-x. [DOI] [PubMed] [Google Scholar]
  56. Irving H. R., Exton J. H. Phosphatidylcholine breakdown in rat liver plasma membranes. Roles of guanine nucleotides and P2-purinergic agonists. J Biol Chem. 1987 Mar 15;262(8):3440–3443. [PubMed] [Google Scholar]
  57. Kanfer J. N. The base exchange enzymes and phospholipase D of mammalian tissue. Can J Biochem. 1980 Dec;58(12):1370–1380. doi: 10.1139/o80-186. [DOI] [PubMed] [Google Scholar]
  58. Kater L. A., Goetzl E. J., Austen K. F. Isolation of human eosinophil phospholipase D. J Clin Invest. 1976 May;57(5):1173–1180. doi: 10.1172/JCI108385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Kennerly D. A. Diacylglycerol metabolism in mast cells. Analysis of lipid metabolic pathways using molecular species analysis of intermediates. J Biol Chem. 1987 Dec 5;262(34):16305–16313. [PubMed] [Google Scholar]
  60. Kester M., Simonson M. S., Mené P., Sedor J. R. Interleukin-1 generates transmembrane signals from phospholipids through novel pathways in cultured rat mesangial cells. J Clin Invest. 1989 Feb;83(2):718–723. doi: 10.1172/JCI113937. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Kinsky S. C., Loader J. E., Benedict S. H. Phorbol ester activation of phospholipase D in human monocytes but not peripheral blood lymphocytes. Biochem Biophys Res Commun. 1989 Jul 31;162(2):788–793. doi: 10.1016/0006-291x(89)92379-6. [DOI] [PubMed] [Google Scholar]
  62. Kiss Z., Anderson W. B. Phorbol ester stimulates the hydrolysis of phosphatidylethanolamine in leukemic HL-60, NIH 3T3, and baby hamster kidney cells. J Biol Chem. 1989 Jan 25;264(3):1483–1487. [PubMed] [Google Scholar]
  63. Kobayashi M., Kanfer J. N. Phosphatidylethanol formation via transphosphatidylation by rat brain synaptosomal phospholipase D. J Neurochem. 1987 May;48(5):1597–1603. doi: 10.1111/j.1471-4159.1987.tb05707.x. [DOI] [PubMed] [Google Scholar]
  64. Kojima I., Kojima K., Kreutter D., Rasmussen H. The temporal integration of the aldosterone secretory response to angiotensin occurs via two intracellular pathways. J Biol Chem. 1984 Dec 10;259(23):14448–14457. [PubMed] [Google Scholar]
  65. Kolesnick R. N., Paley A. E. 1,2-Diacylglycerols and phorbol esters stimulate phosphatidylcholine metabolism in GH3 pituitary cells. Evidence for separate mechanisms of action. J Biol Chem. 1987 Jul 5;262(19):9204–9210. [PubMed] [Google Scholar]
  66. Kolesnick R. N. Thyrotropin-releasing hormone and phorbol esters induce phosphatidylcholine synthesis in GH3 pituitary cells. Evidence for stimulation via protein kinase C. J Biol Chem. 1987 Oct 25;262(30):14525–14530. [PubMed] [Google Scholar]
  67. Lacal J. C., Moscat J., Aaronson S. A. Novel source of 1,2-diacylglycerol elevated in cells transformed by Ha-ras oncogene. Nature. 1987 Nov 19;330(6145):269–272. doi: 10.1038/330269a0. [DOI] [PubMed] [Google Scholar]
  68. Lapetina E. G., Cuatrecasas P. Stimulation of phosphatidic acid production in platelets precedes the formation of arachidonate and parallels the release of serotonin. Biochim Biophys Acta. 1979 May 25;573(2):394–402. doi: 10.1016/0005-2760(79)90072-9. [DOI] [PubMed] [Google Scholar]
  69. Liscovitch M., Amsterdam A. Gonadotropin-releasing hormone activates phospholipase D in ovarian granulosa cells. Possible role in signal transduction. J Biol Chem. 1989 Jul 15;264(20):11762–11767. [PubMed] [Google Scholar]
  70. Liscovitch M., Blusztajn J. K., Freese A., Wurtman R. J. Stimulation of choline release from NG108-15 cells by 12-O-tetradecanoylphorbol 13-acetate. Biochem J. 1987 Jan 1;241(1):81–86. doi: 10.1042/bj2410081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Liscovitch M., Freese A., Blusztajn J. K., Wurtman R. J. Phosphatidylcholine biosynthesis in the neuroblastoma-glioma hybrid cell line NG108-15: stimulation by phorbol esters. J Neurochem. 1986 Dec;47(6):1936–1941. doi: 10.1111/j.1471-4159.1986.tb13111.x. [DOI] [PubMed] [Google Scholar]
  72. Liscovitch M. Phosphatidylethanol biosynthesis in ethanol-exposed NG108-15 neuroblastoma X glioma hybrid cells. Evidence for activation of a phospholipase D phosphatidyl transferase activity by protein kinase C. J Biol Chem. 1989 Jan 25;264(3):1450–1456. [PubMed] [Google Scholar]
  73. Löffelholz K. Receptor regulation of choline phospholipid hydrolysis. A novel source of diacylglycerol and phosphatidic acid. Biochem Pharmacol. 1989 May 15;38(10):1543–1549. doi: 10.1016/0006-2952(89)90299-2. [DOI] [PubMed] [Google Scholar]
  74. MacDonald M. L., Mack K. F., Richardson C. N., Glomset J. A. Regulation of diacylglycerol kinase reaction in Swiss 3T3 cells. Increased phosphorylation of endogenous diacylglycerol and decreased phosphorylation of didecanoylglycerol in response to platelet-derived growth factor. J Biol Chem. 1988 Jan 25;263(3):1575–1583. [PubMed] [Google Scholar]
  75. MacDonald M. L., Mack K. F., Williams B. W., King W. C., Glomset J. A. A membrane-bound diacylglycerol kinase that selectively phosphorylates arachidonoyl-diacylglycerol. Distinction from cytosolic diacylglycerol kinase and comparison with the membrane-bound enzyme from Escherichia coli. J Biol Chem. 1988 Jan 25;263(3):1584–1592. [PubMed] [Google Scholar]
  76. Macara I. G. Elevated phosphocholine concentration in ras-transformed NIH 3T3 cells arises from increased choline kinase activity, not from phosphatidylcholine breakdown. Mol Cell Biol. 1989 Jan;9(1):325–328. doi: 10.1128/mcb.9.1.325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  77. Magnaldo I., L'Allemain G., Chambard J. C., Moenner M., Barritault D., Pouysségur J. The mitogenic signaling pathway of fibroblast growth factor is not mediated through polyphosphoinositide hydrolysis and protein kinase C activation in hamster fibroblasts. J Biol Chem. 1986 Dec 25;261(36):16916–16922. [PubMed] [Google Scholar]
  78. Maroney A. C., Macara I. G. Translocation of diacylglycerol kinase from the cytosol to the membrane in phorbol ester-treated Swiss 3T3 fibroblasts. J Cell Biochem. 1989 Jun;40(2):165–172. doi: 10.1002/jcb.240400205. [DOI] [PubMed] [Google Scholar]
  79. Martin T. W. Formation of diacylglycerol by a phospholipase D-phosphatidate phosphatase pathway specific for phosphatidylcholine in endothelial cells. Biochim Biophys Acta. 1988 Oct 14;962(3):282–296. doi: 10.1016/0005-2760(88)90258-5. [DOI] [PubMed] [Google Scholar]
  80. Martin T. W., Michaelis K. C. Bradykinin stimulates phosphodiesteratic cleavage of phosphatidylcholine in cultured endothelial cells. Biochem Biophys Res Commun. 1988 Dec 30;157(3):1271–1279. doi: 10.1016/s0006-291x(88)81012-x. [DOI] [PubMed] [Google Scholar]
  81. Martin T. W., Michaelis K. P2-purinergic agonists stimulate phosphodiesteratic cleavage of phosphatidylcholine in endothelial cells. Evidence for activation of phospholipase D. J Biol Chem. 1989 May 25;264(15):8847–8856. [PubMed] [Google Scholar]
  82. Martin T. W., Wysolmerski R. B., Lagunoff D. Phosphatidylcholine metabolism in endothelial cells: evidence for phospholipase A and a novel Ca2+-independent phospholipase C. Biochim Biophys Acta. 1987 Feb 14;917(2):296–307. doi: 10.1016/0005-2760(87)90134-2. [DOI] [PubMed] [Google Scholar]
  83. Martinson E. A., Goldstein D., Brown J. H. Muscarinic receptor activation of phosphatidylcholine hydrolysis. Relationship to phosphoinositide hydrolysis and diacylglycerol metabolism. J Biol Chem. 1989 Sep 5;264(25):14748–14754. [PubMed] [Google Scholar]
  84. Matozaki T., Williams J. A. Multiple sources of 1,2-diacylglycerol in isolated rat pancreatic acini stimulated by cholecystokinin. Involvement of phosphatidylinositol bisphosphate and phosphatidylcholine hydrolysis. J Biol Chem. 1989 Sep 5;264(25):14729–14734. [PubMed] [Google Scholar]
  85. Matsuzawa Y., Hostetler K. Y. Properties of phospholipase C isolated from rat liver lysosomes. J Biol Chem. 1980 Jan 25;255(2):646–652. [PubMed] [Google Scholar]
  86. Michell R. H. Inositol phospholipids and cell surface receptor function. Biochim Biophys Acta. 1975 Mar 25;415(1):81–47. doi: 10.1016/0304-4157(75)90017-9. [DOI] [PubMed] [Google Scholar]
  87. Moolenaar W. H., Kruijer W., Tilly B. C., Verlaan I., Bierman A. J., de Laat S. W. Growth factor-like action of phosphatidic acid. Nature. 1986 Sep 11;323(6084):171–173. doi: 10.1038/323171a0. [DOI] [PubMed] [Google Scholar]
  88. Mueller G. C., Fleming M. F., LeMahieu M. A., Lybrand G. S., Barry K. J. Synthesis of phosphatidylethanol--a potential marker for adult males at risk for alcoholism. Proc Natl Acad Sci U S A. 1988 Dec;85(24):9778–9782. doi: 10.1073/pnas.85.24.9778. [DOI] [PMC free article] [PubMed] [Google Scholar]
  89. Mueller H. W., O'Flaherty J. T., Greene D. G., Samuel M. P., Wykle R. L. 1-O-alkyl-linked glycerophospholipids of human neutrophils: distribution of arachidonate and other acyl residues in the ether-linked and diacyl species. J Lipid Res. 1984 Apr;25(4):383–388. [PubMed] [Google Scholar]
  90. Mueller H. W., O'Flaherty J. T., Wykle R. L. Ether lipid content and fatty acid distribution in rabbit polymorphonuclear neutrophil phospholipids. Lipids. 1982 Feb;17(2):72–77. doi: 10.1007/BF02535178. [DOI] [PubMed] [Google Scholar]
  91. Mufson R. A., Okin E., Weinstein I. B. Phorbol esters stimulate the rapid release of choline from prelabelled cells. Carcinogenesis. 1981;2(11):1095–1102. doi: 10.1093/carcin/2.11.1095. [DOI] [PubMed] [Google Scholar]
  92. Muir J. G., Murray A. W. Bombesin and phorbol ester stimulate phosphatidylcholine hydrolysis by phospholipase C: evidence for a role of protein kinase C. J Cell Physiol. 1987 Mar;130(3):382–391. doi: 10.1002/jcp.1041300311. [DOI] [PubMed] [Google Scholar]
  93. Muma N. A., Rowell P. P. A sensitive and specific radioenzymatic assay for the simultaneous determination of choline and phosphatidylcholine. J Neurosci Methods. 1985 Jan;12(3):249–257. doi: 10.1016/0165-0270(85)90008-1. [DOI] [PubMed] [Google Scholar]
  94. Murayama T., Ui M. Phosphatidic acid may stimulate membrane receptors mediating adenylate cyclase inhibition and phospholipid breakdown in 3T3 fibroblasts. J Biol Chem. 1987 Apr 25;262(12):5522–5529. [PubMed] [Google Scholar]
  95. Needleman P., Turk J., Jakschik B. A., Morrison A. R., Lefkowith J. B. Arachidonic acid metabolism. Annu Rev Biochem. 1986;55:69–102. doi: 10.1146/annurev.bi.55.070186.000441. [DOI] [PubMed] [Google Scholar]
  96. Nishihira J., McPhail L. C., O'Flaherty J. T. Stimulus-dependent mobilization of protein kinase C. Biochem Biophys Res Commun. 1986 Jan 29;134(2):587–594. doi: 10.1016/s0006-291x(86)80460-0. [DOI] [PubMed] [Google Scholar]
  97. Nishizuka Y. Studies and perspectives of protein kinase C. Science. 1986 Jul 18;233(4761):305–312. doi: 10.1126/science.3014651. [DOI] [PubMed] [Google Scholar]
  98. Nishizuka Y. The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature. 1988 Aug 25;334(6184):661–665. doi: 10.1038/334661a0. [DOI] [PubMed] [Google Scholar]
  99. Ojima-Uchiyama A., Masuzawa Y., Sugiura T., Waku K., Saito H., Yui Y., Tomioka H. Phospholipid analysis of human eosinophils: high levels of alkylacylglycerophosphocholine (PAF precursor). Lipids. 1988 Aug;23(8):815–817. doi: 10.1007/BF02536227. [DOI] [PubMed] [Google Scholar]
  100. Pagano R. E., Longmuir K. J. Phosphorylation, transbilayer movement, and facilitated intracellular transport of diacylglycerol are involved in the uptake of a fluorescent analog of phosphatidic acid by cultured fibroblasts. J Biol Chem. 1985 Feb 10;260(3):1909–1916. [PubMed] [Google Scholar]
  101. Pai J. K., Siegel M. I., Egan R. W., Billah M. M. Activation of phospholipase D by chemotactic peptide in HL-60 granulocytes. Biochem Biophys Res Commun. 1988 Jan 15;150(1):355–364. doi: 10.1016/0006-291x(88)90528-1. [DOI] [PubMed] [Google Scholar]
  102. Pai J. K., Siegel M. I., Egan R. W., Billah M. M. Phospholipase D catalyzes phospholipid metabolism in chemotactic peptide-stimulated HL-60 granulocytes. J Biol Chem. 1988 Sep 5;263(25):12472–12477. [PubMed] [Google Scholar]
  103. Pelech S. L., Vance D. E. Regulation of phosphatidylcholine biosynthesis. Biochim Biophys Acta. 1984 Jun 25;779(2):217–251. doi: 10.1016/0304-4157(84)90010-8. [DOI] [PubMed] [Google Scholar]
  104. Pessin M. S., Raben D. M. Molecular species analysis of 1,2-diglycerides stimulated by alpha-thrombin in cultured fibroblasts. J Biol Chem. 1989 May 25;264(15):8729–8738. [PubMed] [Google Scholar]
  105. Peter-Riesch B., Fathi M., Schlegel W., Wollheim C. B. Glucose and carbachol generate 1,2-diacylglycerols by different mechanisms in pancreatic islets. J Clin Invest. 1988 Apr;81(4):1154–1161. doi: 10.1172/JCI113430. [DOI] [PMC free article] [PubMed] [Google Scholar]
  106. Preiss J. E., Bell R. M., Niedel J. E. Diacylglycerol mass measurements in stimulated HL-60 phagocytes. J Immunol. 1987 Mar 1;138(5):1542–1545. [PubMed] [Google Scholar]
  107. Preiss J., Loomis C. R., Bishop W. R., Stein R., Niedel J. E., Bell R. M. Quantitative measurement of sn-1,2-diacylglycerols present in platelets, hepatocytes, and ras- and sis-transformed normal rat kidney cells. J Biol Chem. 1986 Jul 5;261(19):8597–8600. [PubMed] [Google Scholar]
  108. Prescott S. M., Majerus P. W. Characterization of 1,2-diacylglycerol hydrolysis in human platelets. Demonstration of an arachidonoyl-monoacylglycerol intermediate. J Biol Chem. 1983 Jan 25;258(2):764–769. [PubMed] [Google Scholar]
  109. Price B. D., Morris J. D., Marshall C. J., Hall A. Stimulation of phosphatidylcholine hydrolysis, diacylglycerol release, and arachidonic acid production by oncogenic ras is a consequence of protein kinase C activation. J Biol Chem. 1989 Oct 5;264(28):16638–16643. [PubMed] [Google Scholar]
  110. Putney J. W., Jr, Weiss S. J., Van De Walle C. M., Haddas R. A. Is phosphatidic acid a calcium ionophore under neurohumoral control? Nature. 1980 Mar 27;284(5754):345–347. doi: 10.1038/284345a0. [DOI] [PubMed] [Google Scholar]
  111. Ragab-Thomas J. M., Hullin F., Chap H., Douste-Blazy L. Pathways of arachidonic acid liberation in thrombin and calcium ionophore A23187-stimulated human endothelial cells: respective roles of phospholipids and triacylglycerol and evidence for diacylglycerol generation from phosphatidylcholine. Biochim Biophys Acta. 1987 Feb 23;917(3):388–397. doi: 10.1016/0005-2760(87)90117-2. [DOI] [PubMed] [Google Scholar]
  112. Rasmussen H., Barrett P. Q. Calcium messenger system: an integrated view. Physiol Rev. 1984 Jul;64(3):938–984. doi: 10.1152/physrev.1984.64.3.938. [DOI] [PubMed] [Google Scholar]
  113. Reibman J., Korchak H. M., Vosshall L. B., Haines K. A., Rich A. M., Weissmann G. Changes in diacylglycerol labeling, cell shape, and protein phosphorylation distinguish "triggering" from "activation" of human neutrophils. J Biol Chem. 1988 May 5;263(13):6322–6328. [PubMed] [Google Scholar]
  114. Rhee S. G., Suh P. G., Ryu S. H., Lee S. Y. Studies of inositol phospholipid-specific phospholipase C. Science. 1989 May 5;244(4904):546–550. doi: 10.1126/science.2541501. [DOI] [PubMed] [Google Scholar]
  115. Rider L. G., Niedel J. E. Diacylglycerol accumulation and superoxide anion production in stimulated human neutrophils. J Biol Chem. 1987 Apr 25;262(12):5603–5608. [PubMed] [Google Scholar]
  116. Rosoff P. M., Savage N., Dinarello C. A. Interleukin-1 stimulates diacylglycerol production in T lymphocytes by a novel mechanism. Cell. 1988 Jul 1;54(1):73–81. doi: 10.1016/0092-8674(88)90181-x. [DOI] [PubMed] [Google Scholar]
  117. Rubin R. Phosphatidylethanol formation in human platelets: evidence for thrombin-induced activation of phospholipase D. Biochem Biophys Res Commun. 1988 Nov 15;156(3):1090–1096. doi: 10.1016/s0006-291x(88)80744-7. [DOI] [PubMed] [Google Scholar]
  118. Saito M., Bourque E., Kanfer J. Phosphatidohydrolase and base-exchange activity of commercial phospholipase D. Arch Biochem Biophys. 1974 Oct;164(2):420–428. doi: 10.1016/0003-9861(74)90051-4. [DOI] [PubMed] [Google Scholar]
  119. Serhan C., Anderson P., Goodman E., Dunham P., Weissmann G. Phosphatidate and oxidized fatty acids are calcium ionophores. Studies employing arsenazo III in liposomes. J Biol Chem. 1981 Mar 25;256(6):2736–2741. [PubMed] [Google Scholar]
  120. Sheikhnejad R. G., Srivastava P. N. Isolation and properties of a phosphatidylcholine-specific phospholipase C from bull seminal plasma. J Biol Chem. 1986 Jun 5;261(16):7544–7549. [PubMed] [Google Scholar]
  121. Shuto S., Ueda S., Itoh H., Endo E., Fukukawa K., Imamura S., Tsujino M., Matsuda A., Ueda T. Synthesis of 5'-phosphatidylnucleosides by phospholipase D-catalyzed transphosphatidylation. Nucleic Acids Symp Ser. 1986;(17):73–76. [PubMed] [Google Scholar]
  122. Simmonds A. C., Halsey M. J. General and local anaesthetics perturb the fusion of phospholipid vesicles. Biochim Biophys Acta. 1985 Mar 14;813(2):331–337. doi: 10.1016/0005-2736(85)90249-4. [DOI] [PubMed] [Google Scholar]
  123. Slivka S. R., Meier K. E., Insel P. A. Alpha 1-adrenergic receptors promote phosphatidylcholine hydrolysis in MDCK-D1 cells. A mechanism for rapid activation of protein kinase C. J Biol Chem. 1988 Sep 5;263(25):12242–12246. [PubMed] [Google Scholar]
  124. Tettenborn C. S., Mueller G. C. 12-O-tetradecanoylphorbol-13-acetate activates phosphatidylethanol and phosphatidylglycerol synthesis by phospholipase D in cell lysates. Biochem Biophys Res Commun. 1988 Aug 30;155(1):249–255. doi: 10.1016/s0006-291x(88)81076-3. [DOI] [PubMed] [Google Scholar]
  125. Tettenborn C. S., Mueller G. C. Phorbol esters activate the pathway for phosphatidylethanol synthesis in differentiating HL-60 cells. Biochim Biophys Acta. 1987 Nov 12;931(2):242–250. doi: 10.1016/0167-4889(87)90212-6. [DOI] [PubMed] [Google Scholar]
  126. Truett A. P., 3rd, Snyderman R., Murray J. J. Stimulation of phosphorylcholine turnover and diacylglycerol production in human polymorphonuclear leukocytes. Novel assay for phosphorylcholine. Biochem J. 1989 Jun 15;260(3):909–913. doi: 10.1042/bj2600909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  127. Truett A. P., 3rd, Verghese M. W., Dillon S. B., Snyderman R. Calcium influx stimulates a second pathway for sustained diacylglycerol production in leukocytes activated by chemoattractants. Proc Natl Acad Sci U S A. 1988 Mar;85(5):1549–1553. doi: 10.1073/pnas.85.5.1549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  128. Tyagi S. R., Burnham D. N., Lambeth J. D. On the biological occurrence and regulation of 1-acyl and 1-O-alkyl-diradylglycerols in human neutrophils. Selective destruction of diacyl species using Rhizopus lipase. J Biol Chem. 1989 Aug 5;264(22):12977–12982. [PubMed] [Google Scholar]
  129. Uhing R. J., Prpic V., Hollenbach P. W., Adams D. O. Involvement of protein kinase C in platelet-activating factor-stimulated diacylglycerol accumulation in murine peritoneal macrophages. J Biol Chem. 1989 Jun 5;264(16):9224–9230. [PubMed] [Google Scholar]
  130. Warden C. H., Friedkin M. Regulation of choline kinase activity and phosphatidylcholine biosynthesis by mitogenic growth factors in 3T3 fibroblasts. J Biol Chem. 1985 May 25;260(10):6006–6011. [PubMed] [Google Scholar]
  131. Welsh C. J., Cao H. T., Chabbott H., Cabot M. C. Vasopressin is the only component of serum-free medium that stimulates phosphatidylcholine hydrolysis and accumulation of diacylglycerol in cultured REF52 cells. Biochem Biophys Res Commun. 1988 Apr 29;152(2):565–572. doi: 10.1016/s0006-291x(88)80075-5. [DOI] [PubMed] [Google Scholar]
  132. Wolf B. A., Easom R. A., Hughes J. H., McDaniel M. L., Turk J. Secretagogue-induced diacylglycerol accumulation in isolated pancreatic islets. Mass spectrometric characterization of the fatty acyl content indicates multiple mechanisms of generation. Biochemistry. 1989 May 16;28(10):4291–4301. doi: 10.1021/bi00436a026. [DOI] [PubMed] [Google Scholar]
  133. Wolf R. A., Gross R. W. Identification of neutral active phospholipase C which hydrolyzes choline glycerophospholipids and plasmalogen selective phospholipase A2 in canine myocardium. J Biol Chem. 1985 Jun 25;260(12):7295–7303. [PubMed] [Google Scholar]
  134. Wright T. M., Rangan L. A., Shin H. S., Raben D. M. Kinetic analysis of 1,2-diacylglycerol mass levels in cultured fibroblasts. Comparison of stimulation by alpha-thrombin and epidermal growth factor. J Biol Chem. 1988 Jul 5;263(19):9374–9380. [PubMed] [Google Scholar]
  135. Yang S. F., Freer S., Benson A. A. Transphosphatidylation by phospholipase D. J Biol Chem. 1967 Feb 10;242(3):477–484. [PubMed] [Google Scholar]
  136. Yu C. L., Tsai M. H., Stacey D. W. Cellular ras activity and phospholipid metabolism. Cell. 1988 Jan 15;52(1):63–71. doi: 10.1016/0092-8674(88)90531-4. [DOI] [PubMed] [Google Scholar]