Abstract
The role of bivalent cations in ATP-stimulated phospholipase D (PLD) activity was investigated in human leukaemic lymphocytes. Cells were labelled with [3H]oleic acid and incubated with extracellular ATP or benzoylbenzoic ATP in the presence of 1 mM Ca2+ and butanol, and PLD activity was assayed by the accumulation of [3H]phosphatidylbutanol ([3H]PBut). ATP stimulated PLD activity in a dose-dependent manner, and the inhibitory effects of suramin, oxidized ATP and extracellular Mg2+ suggested that the effect of ATP was mediated by P2Z purinoceptors known to be present on lymphocytes. Thapsigargin increased cytosolic [Ca2+] but did not stimulate PLD activity, whereas preloading cells with a Ca2+ chelator reduced cytosolic [Ca2+] and, paradoxically, potentiated ATP-stimulated [3H]PBut accumulation. ATP-stimulated [3H]PBut formation was supported by both Ba2+ and Sr2+ when they were substituted for extracellular Ca2+. Addition of EGTA to block bivalent cation influx inhibited the majority of ATP-stimulated PLD activity. Furthermore ATP-stimulated PLD activity showed a linear relationship to extracellular [Ba2+], and ATP-induced 133Ba2+ influx also had a linear dependence on extracellular [Ba2+]. These results suggest that ATP stimulates PLD activity in direct proportion to the influx of bivalent cations through the P2Z-purinoceptor ion channel and that this PLD activity is insensitive to changes in bulk cytosolic [Ca2+].
Full Text
The Full Text of this article is available as a PDF (460.9 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Alonso-Torre S. R., Trautmann A. Calcium responses elicited by nucleotides in macrophages. Interaction between two receptor subtypes. J Biol Chem. 1993 Sep 5;268(25):18640–18647. [PubMed] [Google Scholar]
- BLIGH E. G., DYER W. J. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959 Aug;37(8):911–917. doi: 10.1139/o59-099. [DOI] [PubMed] [Google Scholar]
- Balboa M. A., Firestein B. L., Godson C., Bell K. S., Insel P. A. Protein kinase C alpha mediates phospholipase D activation by nucleotides and phorbol ester in Madin-Darby canine kidney cells. Stimulation of phospholipase D is independent of activation of polyphosphoinositide-specific phospholipase C and phospholipase A2. J Biol Chem. 1994 Apr 8;269(14):10511–10516. [PubMed] [Google Scholar]
- Barry V. A., Cheek T. R. Extracellular ATP triggers two functionally distinct calcium signalling pathways in PC12 cells. J Cell Sci. 1994 Feb;107(Pt 2):451–462. doi: 10.1242/jcs.107.2.451. [DOI] [PubMed] [Google Scholar]
- Billah M. M. Phospholipase D and cell signaling. Curr Opin Immunol. 1993 Feb;5(1):114–123. doi: 10.1016/0952-7915(93)90090-f. [DOI] [PubMed] [Google Scholar]
- Blache D., Ciavatti M. Effects of organic and inorganic Ca antagonists on rat platelet arachidonic acid metabolism in the presence of Ca2+, Sr2+ and Ba2+. Mol Cell Biochem. 1989 Feb 21;85(2):191–196. doi: 10.1007/BF00577114. [DOI] [PubMed] [Google Scholar]
- Blache D., Ciavatti M. Rat platelet arachidonate metabolism in the presence of Ca2+, Sr2+ and Ba2+: studies using intact platelets and semi-purified phospholipase A2. Biochim Biophys Acta. 1987 Oct 17;921(3):541–551. doi: 10.1016/0005-2760(87)90082-8. [DOI] [PubMed] [Google Scholar]
- Bretschneider F., Klapperstück M., Löhn M., Markwardt F. Nonselective cationic currents elicited by extracellular ATP in human B-lymphocytes. Pflugers Arch. 1995 Mar;429(5):691–698. doi: 10.1007/BF00373990. [DOI] [PubMed] [Google Scholar]
- Brooks S. P., Storey K. B. Bound and determined: a computer program for making buffers of defined ion concentrations. Anal Biochem. 1992 Feb 14;201(1):119–126. doi: 10.1016/0003-2697(92)90183-8. [DOI] [PubMed] [Google Scholar]
- Brown H. A., Gutowski S., Moomaw C. R., Slaughter C., Sternweis P. C. ADP-ribosylation factor, a small GTP-dependent regulatory protein, stimulates phospholipase D activity. Cell. 1993 Dec 17;75(6):1137–1144. doi: 10.1016/0092-8674(93)90323-i. [DOI] [PubMed] [Google Scholar]
- Cockcroft S., Thomas G. M., Fensome A., Geny B., Cunningham E., Gout I., Hiles I., Totty N. F., Truong O., Hsuan J. J. Phospholipase D: a downstream effector of ARF in granulocytes. Science. 1994 Jan 28;263(5146):523–526. doi: 10.1126/science.8290961. [DOI] [PubMed] [Google Scholar]
- Cook S. J., Wakelam M. J. Phospholipases C and D in mitogenic signal transduction. Rev Physiol Biochem Pharmacol. 1992;119:13–45. doi: 10.1007/3540551921_2. [DOI] [PubMed] [Google Scholar]
- Dubyak G. R., De Young M. B. Intracellular Ca2+ mobilization activated by extracellular ATP in Ehrlich ascites tumor cells. J Biol Chem. 1985 Sep 5;260(19):10653–10661. [PubMed] [Google Scholar]
- Dubyak G. R., el-Moatassim C. Signal transduction via P2-purinergic receptors for extracellular ATP and other nucleotides. Am J Physiol. 1993 Sep;265(3 Pt 1):C577–C606. doi: 10.1152/ajpcell.1993.265.3.C577. [DOI] [PubMed] [Google Scholar]
- Etter E. F., Kuhn M. A., Fay F. S. Detection of changes in near-membrane Ca2+ concentration using a novel membrane-associated Ca2+ indicator. J Biol Chem. 1994 Apr 1;269(13):10141–10149. [PubMed] [Google Scholar]
- Exton J. H. Phosphatidylcholine breakdown and signal transduction. Biochim Biophys Acta. 1994 Apr 14;1212(1):26–42. doi: 10.1016/0005-2760(94)90186-4. [DOI] [PubMed] [Google Scholar]
- Freeman E. J., Chisolm G. M., Tallant E. A. Role of calcium and protein kinase C in the activation of phospholipase D by angiotensin II in vascular smooth muscle cells. Arch Biochem Biophys. 1995 May 10;319(1):84–92. doi: 10.1006/abbi.1995.1269. [DOI] [PubMed] [Google Scholar]
- Gordon J. L. Extracellular ATP: effects, sources and fate. Biochem J. 1986 Jan 15;233(2):309–319. doi: 10.1042/bj2330309. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Greenberg S., Di Virgilio F., Steinberg T. H., Silverstein S. C. Extracellular nucleotides mediate Ca2+ fluxes in J774 macrophages by two distinct mechanisms. J Biol Chem. 1988 Jul 25;263(21):10337–10343. [PubMed] [Google Scholar]
- Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
- Huang C., Wykle R. L., Daniel L. W., Cabot M. C. Identification of phosphatidylcholine-selective and phosphatidylinositol-selective phospholipases D in Madin-Darby canine kidney cells. J Biol Chem. 1992 Aug 25;267(24):16859–16865. [PubMed] [Google Scholar]
- Kessels G. C., Roos D., Verhoeven A. J. fMet-Leu-Phe-induced activation of phospholipase D in human neutrophils. Dependence on changes in cytosolic free Ca2+ concentration and relation with respiratory burst activation. J Biol Chem. 1991 Dec 5;266(34):23152–23156. [PubMed] [Google Scholar]
- Lew V. L., Tsien R. Y., Miner C., Bookchin R. M. Physiological [Ca2+]i level and pump-leak turnover in intact red cells measured using an incorporated Ca chelator. Nature. 1982 Jul 29;298(5873):478–481. doi: 10.1038/298478a0. [DOI] [PubMed] [Google Scholar]
- Lin P., Gilfillan A. M. The role of calcium and protein kinase C in the IgE-dependent activation of phosphatidylcholine-specific phospholipase D in a rat mast (RBL 2H3) cell line. Eur J Biochem. 1992 Jul 1;207(1):163–168. doi: 10.1111/j.1432-1033.1992.tb17033.x. [DOI] [PubMed] [Google Scholar]
- McMillian M. K., Soltoff S. P., Cantley L. C., Rudel R., Talamo B. R. Two distinct cytosolic calcium responses to extracellular ATP in rat parotid acinar cells. Br J Pharmacol. 1993 Feb;108(2):453–461. doi: 10.1111/j.1476-5381.1993.tb12825.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Metz S. A., Dunlop M. Stimulation of insulin release by phospholipase D. A potential role for endogenous phosphatidic acid in pancreatic islet function. Biochem J. 1990 Sep 1;270(2):427–435. doi: 10.1042/bj2700427. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murgia M., Hanau S., Pizzo P., Rippa M., Di Virgilio F. Oxidized ATP. An irreversible inhibitor of the macrophage purinergic P2Z receptor. J Biol Chem. 1993 Apr 15;268(11):8199–8203. [PubMed] [Google Scholar]
- Murrin R. J., Boarder M. R. Neuronal "nucleotide" receptor linked to phospholipase C and phospholipase D? Stimulation of PC12 cells by ATP analogues and UTP. Mol Pharmacol. 1992 Mar;41(3):561–568. [PubMed] [Google Scholar]
- Nally J. E., Muir T. C., Guild S. B. The effects of noradrenaline and adenosine 5'-triphosphate on polyphosphoinositide and phosphatidylcholine hydrolysis in arterial smooth muscle. Br J Pharmacol. 1992 Aug;106(4):865–870. doi: 10.1111/j.1476-5381.1992.tb14426.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Olson S. C., Bowman E. P., Lambeth J. D. Phospholipase D activation in a cell-free system from human neutrophils by phorbol 12-myristate 13-acetate and guanosine 5'-O-(3-thiotriphosphate). Activation is calcium dependent and requires protein factors in both the plasma membrane and cytosol. J Biol Chem. 1991 Sep 15;266(26):17236–17242. [PubMed] [Google Scholar]
- Pfeilschifter J., Merriweather C. Extracellular ATP and UTP activation of phospholipase D is mediated by protein kinase C-epsilon in rat renal mesangial cells. Br J Pharmacol. 1993 Oct;110(2):847–853. doi: 10.1111/j.1476-5381.1993.tb13890.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pizzo P., Zanovello P., Bronte V., Di Virgilio F. Extracellular ATP causes lysis of mouse thymocytes and activates a plasma membrane ion channel. Biochem J. 1991 Feb 15;274(Pt 1):139–144. doi: 10.1042/bj2740139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Purkiss J. R., Boarder M. R. Stimulation of phosphatidate synthesis in endothelial cells in response to P2-receptor activation. Evidence for phospholipase C and phospholipase D involvement, phosphatidate and diacylglycerol interconversion and the role of protein kinase C. Biochem J. 1992 Oct 1;287(Pt 1):31–36. doi: 10.1042/bj2870031. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Purkiss J., Owen P. J., Jones J. A., Boarder M. R. Stimulation of phosphatidic acid synthesis in bovine aortic endothelial cells in response to activation of P2-purinergic receptors. Biochem Pharmacol. 1992 Mar 17;43(6):1235–1242. doi: 10.1016/0006-2952(92)90497-7. [DOI] [PubMed] [Google Scholar]
- Ransom J. T., DiGiusto D. L., Cambier J. C. Single cell analysis of calcium mobilization in anti-immunoglobulin-stimulated B lymphocytes. J Immunol. 1986 Jan;136(1):54–57. [PubMed] [Google Scholar]
- Rooney S. A., Gobran L. I. Activation of phospholipase D in rat type II pneumocytes by ATP and other surfactant secretagogues. Am J Physiol. 1993 Feb;264(2 Pt 1):L133–L140. doi: 10.1152/ajplung.1993.264.2.L133. [DOI] [PubMed] [Google Scholar]
- Scharff O., Foder B., Thastrup O., Hofmann B., Møller J., Ryder L. P., Jacobsen K. D., Langhoff E., Dickmeiss E., Christensen S. B. Effect of thapsigargin on cytoplasmic Ca2+ and proliferation of human lymphocytes in relation to AIDS. Biochim Biophys Acta. 1988 Dec 9;972(3):257–264. doi: 10.1016/0167-4889(88)90200-5. [DOI] [PubMed] [Google Scholar]
- Schilling W. P., Rajan L., Strobl-Jager E. Characterization of the bradykinin-stimulated calcium influx pathway of cultured vascular endothelial cells. Saturability, selectivity, and kinetics. J Biol Chem. 1989 Aug 5;264(22):12838–12848. [PubMed] [Google Scholar]
- Shukla S. D., Halenda S. P. Phospholipase D in cell signalling and its relationship to phospholipase C. Life Sci. 1991;48(9):851–866. doi: 10.1016/0024-3205(91)90031-6. [DOI] [PubMed] [Google Scholar]
- Siddiqui R. A., Exton J. H. Phospholipid base exchange activity in rat liver plasma membranes. Evidence for regulation by G-protein and P2y-purinergic receptor. J Biol Chem. 1992 Mar 25;267(9):5755–5761. [PubMed] [Google Scholar]
- Thastrup O. Role of Ca2(+)-ATPases in regulation of cellular Ca2+ signalling, as studied with the selective microsomal Ca2(+)-ATPase inhibitor, thapsigargin. Agents Actions. 1990 Jan;29(1-2):8–15. doi: 10.1007/BF01964706. [DOI] [PubMed] [Google Scholar]
- Whatmore J., Cronin P., Cockcroft S. ARF1-regulated phospholipase D in human neutrophils is enhanced by PMA and MgATP. FEBS Lett. 1994 Sep 26;352(2):113–117. doi: 10.1016/0014-5793(94)00930-9. [DOI] [PubMed] [Google Scholar]
- Wiley J. S., Chen J. R., Snook M. B., Jamieson G. P. The P2Z-purinoceptor of human lymphocytes: actions of nucleotide agonists and irreversible inhibition by oxidized ATP. Br J Pharmacol. 1994 Jul;112(3):946–950. doi: 10.1111/j.1476-5381.1994.tb13172.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wiley J. S., Chen R., Jamieson G. P. The ATP4- receptor-operated channel (P2Z class) of human lymphocytes allows Ba2+ and ethidium+ uptake: inhibition of fluxes by suramin. Arch Biochem Biophys. 1993 Aug 15;305(1):54–60. doi: 10.1006/abbi.1993.1392. [DOI] [PubMed] [Google Scholar]
- Wiley J. S., Chen R., Wiley M. J., Jamieson G. P. The ATP4- receptor-operated ion channel of human lymphocytes: inhibition of ion fluxes by amiloride analogs and by extracellular sodium ions. Arch Biochem Biophys. 1992 Feb 1;292(2):411–418. doi: 10.1016/0003-9861(92)90010-t. [DOI] [PubMed] [Google Scholar]
- Wiley J. S., Dubyak G. R. Extracellular adenosine triphosphate increases cation permeability of chronic lymphocytic leukemic lymphocytes. Blood. 1989 Apr;73(5):1316–1323. [PubMed] [Google Scholar]
- Wiley J. S., Jamieson G. P., Mayger W., Cragoe E. J., Jr, Jopson M. Extracellular ATP stimulates an amiloride-sensitive sodium influx in human lymphocytes. Arch Biochem Biophys. 1990 Aug 1;280(2):263–268. doi: 10.1016/0003-9861(90)90328-v. [DOI] [PubMed] [Google Scholar]
- Wiley J. S., Taupin J., Jamieson G. P., Snook M., Sawyer W. H., Finch L. R. Cytosine arabinoside transport and metabolism in acute leukemias and T cell lymphoblastic lymphoma. J Clin Invest. 1985 Feb;75(2):632–642. doi: 10.1172/JCI111741. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu H., James-Kracke M. R., Halenda S. P. Direct relationship between intracellular calcium mobilization and phospholipase D activation in prostaglandin E-stimulated human erythroleukemia cells. Biochemistry. 1992 Apr 7;31(13):3370–3377. doi: 10.1021/bi00128a010. [DOI] [PubMed] [Google Scholar]
- Xie M. S., Dubyak G. R. Guanine-nucleotide- and adenine-nucleotide-dependent regulation of phospholipase D in electropermeabilized HL-60 granulocytes. Biochem J. 1991 Aug 15;278(Pt 1):81–89. doi: 10.1042/bj2780081. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xie M. S., Jacobs L. S., Dubyak G. R. Regulation of phospholipase D and primary granule secretion by P2-purinergic- and chemotactic peptide-receptor agonists is induced during granulocytic differentiation of HL-60 cells. J Clin Invest. 1991 Jul;88(1):45–54. doi: 10.1172/JCI115303. [DOI] [PMC free article] [PubMed] [Google Scholar]
- el-Moatassim C., Dubyak G. R. A novel pathway for the activation of phospholipase D by P2z purinergic receptors in BAC1.2F5 macrophages. J Biol Chem. 1992 Nov 25;267(33):23664–23673. [PubMed] [Google Scholar]
- el-Moatassim C., Dubyak G. R. Dissociation of the pore-forming and phospholipase D activities stimulated via P2z purinergic receptors in BAC1.2F5 macrophages. Product inhibition of phospholipase D enzyme activity. J Biol Chem. 1993 Jul 25;268(21):15571–15578. [PubMed] [Google Scholar]
