Skip to main content
Log in

Modeling degranulation with liposomes: Effect of lipid composition on membrane fusion

  • Articles
  • Published:
The Journal of Membrane Biology Aims and scope Submit manuscript

Abstract

Degranulation involves the regulated fusion of granule membrane with plasma membrane. To study the role of lipid composition in degranulation, large unilamellar vesicles (LUVs) of increasing complexity in lipid compositions were constructed and tested for Ca2+-mediated lipid and contents mixing. Lipid-mixing rates of LUVs composed of phosphatidylethanolamine (PE) and phosphatidylserine (PS) were strongly decreased by the addition of either phosphatidylcholine (PC) or sphingomyelin (SM), while phosphatidylinositol (PI) had little effect. “Complex” LUVs of PC∶PE∶SM∶PI∶PS (24∶27∶20∶16∶13, designed to emulate neutrophil plasma membranes) also showed very low rates of both lipid mixing and contents mixing. The addition of cholesterol significantly lowered the Ca2+ threshold for contents mixing and increased the maximum rates of both lipid and contents mixing in a dose-dependent manner. Membrane remodeling, which occurs in neutrophil plasma membranes upon stimulation, was simulated by incorporating low levels of phosphatidic acid (PA) or a diacylglycerol (DAG) into complex LUVs containing 50% cholesterol. The addition of PA both lowered the Ca2+ threshold and increased the rate of contents mixing in a dose-dependent manner, while the DAG had no significant effect. The interaction of dissimilar LUVs was also examined. Contents-mixing rates of LUVs of two different cholesterol contents were intermediate between the rates observed for the LUVs of identical composition. Thus, cholesterol needed to be present in only one fusing partner to enhance fusion. However, for PA to stimulate fusion, it had to be present in both sets of LUVs. These results suggest that the rate of degranulation may be increased by a rise in the cholesterol level of either the inner face of the plasma membrane or the outer face of the granule membrane. Further, the production of PA can promote fusion, and hence degranulation, whereas the subsequent conversion of PA to DAG may reverse this promotional effect.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

ANTS:

8-aminonaphthalene-1,3,6-trisulfonic acid

DiC8 :

1,2-dioctanoyl-sn-glycerol

DPX:

p-xylene-bis-pyridinium bromide

LUV:

large unilamellar vesicle

PA:

phosphatidic acid

PC:

phosphatidylcholine

PE:

phosphatidylethanolamine

PI:

phosphatidylinositol

PS:

phosphatidylserine

R18:

octadecyl rhodamine

SM:

sphingomyelin

References

  • Agwu, D.E., McPhail, L.C., Chabot, M.C., Daniel, L.W., Wykle, R.L., McCall, C.E. 1989. Choline-linked phosphoglycerides. A source of phosphatidic acid and diglycerides in stimulated neutrophils. J. Biol. Chem. 264:1405–1413

    Google Scholar 

  • Barinaga, M. 1993. Secrets of secretion revealed. Science 260:487–489

    Google Scholar 

  • Bennett, M.K., Scheller, R.H. 1993. The molecular machinery for secretion is conserved from yeast to neurons. Proc. Natl. Acad. Sci. USA 90:2559–2563

    Google Scholar 

  • Bental, M., Wilschut, J., Scholma, J., Nir, S. 1987. Ca2+-induced fusion of large unilamellar phosphatidylserine/cholesterol vesicles. Biochim. Biophys. Acta 898:239–247

    Google Scholar 

  • Bentz, J., Düzgünes, N., Nir, S. 1983. Kinetics of divalent cation induced fusion of phosphatidylserine vesicles: correlation between fusogenic capacities and binding affinities. Biochemistry 22:3320–3330

    Google Scholar 

  • Bers, D.M. 1982. A simple method for the accurate determination of free (Ca) in Ca-EGTA solutions. Am. J. Physiol 242:C404-C408

    Google Scholar 

  • Billah, M.M., Eckel, S., Mullmann, T.J., Egan, R.W., Siegel, M.I. 1989. Phosphatidylcholine hydrolysis by phospholipase D determines phosphatidate and diglyceride levels in chemotactic peptidestimulated human neutrophils. Involvement of phosphatidate phosphohydrolase in signal transduction. J. Biol. Chem. 264:17069–17077

    Google Scholar 

  • Blackwood, R.A., Ernst, J.D. 1990. Characterization of Ca2+-dependent phospholipid binding, vesicle aggregation and membrane fusion by annexins. Biochem. J. 266:195–200

    Google Scholar 

  • Boonen, G.J.J.C., De Koster, B.M., Elferink, J.G.R. 1993. Activation of neutrophil migration by dioctanoyl-sn-glycerol and fMet-LeuPhe is controlled by different pathways. Agents Actions 38Suppl.C:C130-C132

    Google Scholar 

  • Braun, G., Lelkes, P.I., Nir, S. 1985. Effect of cholesterol on Ca2+-induced aggregation and fusion of sonicated phosphatidylserine/cholesterol vesicles. Biochim. Biophys. Acta 812:688–694

    Google Scholar 

  • Breisblatt, W., Ohki, S. 1976. Fusion in phospholipid spherical membranes: II. Effect of cholesterol, divalent ions and pH. J. Membrane Biol. 29:127–146

    Google Scholar 

  • Chaudhury, M.K., Ohki, S. 1981. Correlation between membrane expansion and temperature-induced membrane fusion. Biochim. Biophys. Acta 642:365–374

    Google Scholar 

  • Clary, D.O., Griff, I.C., Rothman, J.E. 1990. SNAPs, a family of NSF attachment proteins involved in intracellular membrane fusion in animals and yeast. Cell 61:709–721

    Google Scholar 

  • Cockcroft, S. 1984. Ca2+-dependent conversion of phosphatidylinositol to phosphatidate in neutrophils stimulated with fMet-LeuPhe or ionophore A23187. Biochim. Biophys. Acta 795:37–46

    Google Scholar 

  • Cockcroft, S. 1992. G-protein-regulated phospholipases C, D and A2-mediated signalling in neutrophils. Biochim. Biophys. Acta Rev. Biomembr. 1113:135–160

    Google Scholar 

  • Cockcroft, S., Bennett, J.P., Gomperts, B.D. 1980. Stimulus-secretion coupling in rabbit neutrophils is not mediated by phosphatidylinositol breakdown. Nature 288:275–277

    Google Scholar 

  • Connor, J., Yatvin, M.B., Huang, L. 1984. pH-sensitive liposomes: Acid-induced liposome fusion. Proc. Natl. Acad. Sci. USA 81:1715–1718

    Google Scholar 

  • Creutz, C.E. 1992. The annexins and exocytosis. Science 258:924–930

    Google Scholar 

  • Cullis, P.R., Hope, M.J., De Kruijff, B., Verkleij, A.J., Tilcock, C.P.S. 1985. Structural properties and functional roles of phospholipids in biological membranes. In: Phospholipids and Cellular Regulation. J.F. Kuo, editor. pp. 3–59. CRC, Boca Raton, FL

    Google Scholar 

  • De Camilli, P. 1993. Secretion: Exocytosis goes with a SNAP. Nature 364:387–388

    Google Scholar 

  • Delia Bianca, V., Grzeskowiak, M., Lissandrini, D., Rossi, F. 1991. Source and role of diacylglycerol formed during phagocytosis of opsonized yeast particles and associated respiratory burst in human neutrophils. Biochem. Biophys. Res. Commun. 177:948–955

    Google Scholar 

  • Devaux, P.F., Mathivet, L., Cribier, S., Farge, E. 1993. How lipid asymmetry can make vesicles fusion-competent by inhibition of the thermal undulations. Biochem. Soc. Trans. 21:276–280

    Google Scholar 

  • Diez, E., Balsinde, J., Mollinedo, F. 1990. Subcellular distribution of fatty acids, phospholipids and phospholipase A2 in human neutrophils. Biochim. Biophys. Acta Lipids Lipid Metab. 1047:83–89

    Google Scholar 

  • Düzgünes, N., Hong, K., Baldwin, P.A., Bentz, J., Nir, S., Papahadjopoulos, D. 1987. Fusion of phospholipid vesicles induced by divalent cations and protons. Modulation by phase transitions, free fatty acids, monovalent cations, and polyamines. In: Cell Fusion. A.E. Sower, editor. pp. 241–267. Plenum, New York

    Google Scholar 

  • Düzgünes, N., Wilschut, J., Fraley, R., Papahadjopoulos, D. 1981. Studies on the mechanism of membrane fusion: Role of headgroup composition in calcium- and magnesium-induced fusion of mixed phospholipid vesicles. Biochim. Biophys. Acta 642:182–195

    Google Scholar 

  • Eastman, S.J., Hope, M.J., Wong, K.F., Cullis, P.R. 1992. Influence of phospholipid asymmetry on fusion between large unilamellar vesicles. Biochemistry 31:4262–4268

    Google Scholar 

  • Eberhard, D.A., Cooper, C.L., Low, M.G., Holz, R.W. 1990. Evidence that the inositol phospholipids are necessary for exocytosis. Loss of inositol phospholipids and inhibition of secretion in permeabilized cells caused by a bacterial phospholipase C and removal of ATP. Biochem. J. 268:15–25

    Google Scholar 

  • Edwardson, J.M., MacLean, C.M., Law, G.J. 1993. Synthetic peptides of the rab3 effector domain stimulate a membrane fusion event involved in regulated exocytosis. FEBS Lett. 320:52–56

    Google Scholar 

  • Etemadi, A.-H. 1980. Membrane asymmetry. A survey and critical appraisal of the methodology. II. Methods for assessing unequal distribution of lipids. Biochim. Biophys. Acta 604:423–475

    Google Scholar 

  • Evans, E., Needham, D. 1986. Giant vesicle bilayers composed of mixtures of lipids, cholesterol and polypeptides. Thermomechanical and (mutual) adherence properties. Faraday Discuss. Chem. Soc. 81:267–280

    Google Scholar 

  • Francis, J.W., Balazovich, K.J., Smolen, J.E., Margolis, D.I., Boxer, L.A. 1992. Human neutrophil annexin I promotes granule aggregation and modulates Ca2+-dependent membrane fusion. J. Clin. Invest. 90:537–544

    Google Scholar 

  • Francis, J.W., Smolen, J.E., Balazovich, K.J., Sandborg, R.R., Boxer, L.A. 1990. Calcium-dependent fusion of the plasma membrane fraction from human neutrophils with liposomes. Biochim. Biophys. Acta 1025:1–9

    Google Scholar 

  • Gomez-Fernandez, J.C., Aranda, F.J., Micol, V., Villalain, L, Ortiz, A. 1989. Effect of diacylglycerols on calcium-induced fusion of phosphatidylserine/phosphatidylcholine vesicles. Biochem. Soc. Trans. 17:957–960

    Google Scholar 

  • Grubbs, R.D., Maguire, M.E. 1987. Magnesium as a regulatory cation: Criteria and evaluation. Magnesium 6:113–127

    Google Scholar 

  • Hope, M.J., Walker, D.C., Cullis, P.R. 1983. Ca2+ and pH induced fusion of small unilamellar vesicles consisting of phosphatidyl-ethanolamine and negatively charged phospholipids: a freeze fracture study. Biochem. Biophys. Res. Commun. 110:15–22

    Google Scholar 

  • Horkovics-Kovats, S., Traub, P. 1990. Specific interaction of the intermediate filament protein vimentin and its isolated N-terminus with negatively charged phospholipids as determined by vesicle aggregation, fusion, and leakage measurements. Biochemistry 29:8652–8657

    Google Scholar 

  • Jaconi, M.E.E., Theler, J.M., Schlegel, W., Appel, R.D., Wright, S.D., Lew, P.D. 1991. Multiple elevations of cytosolic-free Ca2+ in human neutrophils: Initiation by adherence receptor of the integrin family. J. Cell Biol. 112:1249–1257

    Google Scholar 

  • Kielian, M.C., Helenius, A. 1984. Role of cholesterol in fusion of Semliki Forest virus with membranes. J. Virol. 52:281–283

    Google Scholar 

  • MacLean, C.M., Law, G.J., Edwardson, J.M. 1993. Stimulation of exocytotic membrane fusion by modified peptides of the rab3 effector domain: Re-evaluation of the role of rab3 in regulated exocytosis. Biochem. J. 294:325–328

    Google Scholar 

  • Mason, R.J., Stossel, T.P., Vaughan, M. 1972. Lipids of alveolar macrophages, polymorphonuclear leukocytes, and their phagocytic vesicles. J. Clin. Invest. 51:2399–2407

    Google Scholar 

  • Meers, P., Ernst, J.D., Düzgünes, N., Hong, K.L., Fedor, J., Goldstein, I.M., Papahadjopoulos, D. 1987. Synexin-like proteins from human polymorphonuclear leukocytes. Identification and characterization of granule-aggregating and membrane-fusing activities. J. Biol. Chem. 262:7850–7858

    Google Scholar 

  • Morrison, W.R. 1964. A fast, simple and reliable method for the microdetermination of phosphorus in biological materials. Anal. Biochem. 7:218–224

    Google Scholar 

  • Mueller, H.W., O'Flaherty, J.T., Greene, D.G., Samuel, M.P., Wykle, R.L. 1984. 1-O-Alkyl-linked glycerophospholipids of human neutrophils: distribution or arachidonate and other acyl residues in the ether-linked and diacyl species. J. Lipid Res. 25:383–388

    Google Scholar 

  • Nachman, R., Hirsch, J.G., Baggiolini, M. 1972. Studies on isolated membrane of azurophil and specific granules from rabbit polymorphonuclear leukocytes. J. Cell Biol. 54:133–140

    Google Scholar 

  • Nieva, J.L., Goni, F.M., Alonso, A. 1989. Liposome fusion catalytically induced by phospholipase C. Biochemistry 28:7364–7367

    Google Scholar 

  • Papahadjopoulos, D., Poste, G., Schaeffer, B.E., Vail, W.J. 1974. Membrane fusion and molecular segregation in phospholipid vesicles. Biochim. Biophys. Acta 352:10–28

    Google Scholar 

  • Papahadjopoulos, D., Nir, S., Düzgünes, N. 1990. Molecular mechanisms of calcium-induced membrane fusion. J. Bioenerg. Biomemb. 22:157–179

    Google Scholar 

  • Park, J.-B., Lee, T.-H., Kim, H. 1992. Fusion of phospholipid vesicles induced by phospholipase D in the presence of calcium ion. Biochem. Int. 27:417–422

    Google Scholar 

  • Raja, K.B., Leach, P.M., Peters, G.P., McCarthy, D., Peters, TJ. 1982. The concentration and subcellular localisation of zinc, magnesium and calcium in human polymorphonuclear leukocytes. Clin. Chim. Acta 123:19–26

    Google Scholar 

  • Rand, R.P., Parsegian, V.A. 1986. Mimicry and mechanism in phospholipid models of membrane fusion. Annu. Rev. Physiol. 48:201–212

    Google Scholar 

  • Rosenthal, M.D., Lattanzio, K.S., Franson, R.C. 1993. 1,3-Dioctanoylglycerol modulates arachidonate mobilization in human neutrophils and its inhibition by PGBx: evidence of a protein-kinase-C-independent role for diacylglycerols in signal transduction. Biochim. Biophys. Acta Mol. Cell Res. 1177:79–86

    Google Scholar 

  • Rothman, I.E., Orci, L. 1990. Movement of proteins through the Golgi stack: a molecular dissection of vesicular transport. FASEB J. 4:1460–1468

    Google Scholar 

  • Santini, M.T., Indovina, P.L., Cantafora, A., Blotta, I. 1990. The cesium-induced delay in myoblast membrane fusion is accompanied by changes in isolated membrane lipids. Biochim. Biophys. Acta 1023:298–304

    Google Scholar 

  • Sawyer, D.W., Sullivan, J.A., Mandell, G.L. 1985. Intracellular free calcium localization in neutrophils during phagocytosis. Science 230:663–666

    Google Scholar 

  • Schroeder, F., Nemecz, G. 1990. Transmembrane cholesterol distribution. In: Advances in Cholesterol Research. M. Esfahani and J.B. Swaney, editors. pp. 47–87. Telford, Caldwell, NJ

    Google Scholar 

  • Serhan, C.N., Broekman, M.J., Korchak, H.M., Marcus, A.J., Weissmann, G. 1982. Endogenous phospholipid metabolism in stimulated neutrophils. Differential activation by FMLP and PMA. Biochem. Biophys. Res. Commun. 107:951–958

    Google Scholar 

  • Sessions, A., Horwitz, A.G. 1983. Differentiation-related differences in the plasma membrane phospholipid asymmetry of myogenic and fibrogenic cells. Biochim. Biophys. Acta 728:103–111

    Google Scholar 

  • Siegel, D.P., Banschbach, J., Alford, D., Ellens, H., Lis, L.J., Quinn, P.J., Yeagle, P.L., Bentz, J. 1989. Physiological levels of diacylglycerols in phospholipid membranes induce membrane fusion and stabilize inverted phases. Biochemistry 28:3703–3709

    Google Scholar 

  • Smolen, J.E. 1992. Neutrophil signal transduction: Calcium, kinases, and fusion. J. Lab. Clin. Med. 120:527–532

    Google Scholar 

  • Smolen, J.E., Sandborg, R.R. 1990. Ca2+-induced secretion by electropermeabilized human neutrophils. The roles of Ca2+, nucleotides and protein kinase C. Biochim. Biophys. Acta 1052:133–142

    Google Scholar 

  • Smolen, J.E., Shohet, S.B. 1974. Remodeling of granulocyte membrane fatty acids during phagocytosis. J. Clin. Invest. 53:726–734

    Google Scholar 

  • Söllner, T., Whiteheart, S.W., Brunner, M., Erdjument-Bromage, H., Geromanos, S., Tempst, P., Rothman, J.E. 1993. SNAP receptors implicated in vesicle targeting and fusion. Nature 362:318–324

    Google Scholar 

  • Stamatotos, L., Silvius, J.R. 1987. Effects of cholesterol on the divalent cation-mediated interactions of vesicles containing amino and choline phospholipids. Biochim. Biophys. Acta 905:81–90

    Google Scholar 

  • Sundler, R., Düzgünes, N., Papahadjopoulos, D. 1981. Control of membrane fusion by phospholipid head groups. II. The role of phosphatidylethanolamine in mixtures with phosphatidate and phosphatidylinositol. Biochim. Biophys. Acta 649:751–758

    Google Scholar 

  • Sundler, R., Papahadjopoulos, D. 1981. Control of membrane fusion by phospholipid head groups. I. Phosphatidate/phosphatidylinositol specificity. Biochim. Biophys. Acta 649:743–750

    Google Scholar 

  • Tou, J., Jeter, J.R., Jr., Dola, C.P., Venkatesh, S. 1991. Accumulation of phosphatidic acid mass and increased de novo synthesis of glycerolipids in platelet-activating-factor-activated human neutrophils. Biochem. J. 280:625–629

    Google Scholar 

  • Uster, P.S., Deamer, D.W. 1981. Fusion competence of phosphatidylserine-containing liposomes quantitatively measured by a fluorescence resonance energy transfer assay. Arch. Biochem. Biophys. 209:385–395

    Google Scholar 

  • Verhoven, B., Schlegel, R.A., Williamson, P. 1992. Rapid loss and restoration of lipid asymmetry by different pathways in resealed erythrocyte ghosts. Biochim. Biophys. Acta Bio-Membr. 1104:15–23

    Google Scholar 

  • Werb, Z., Cohn, Z.A. 1972. Plasma membrane synthesis in the macrophage following phagocytosis of polystyrene latex particles. J. Biol. Chem. 247:2439–2446

    Google Scholar 

  • Woodin, A.M., Wieneke, A.A. 1966. Composition and properties of a cell-membrane fraction from the polymorphonuclear leucocyte. Biochem. J. 99:493–500

    Google Scholar 

  • Zaks, W.J., Creutz, C.E. 1990. Evaluation of the annexins as potential mediators of membrane fusion in exocytosis. J. Bioenerg. Biomemb. 22:97–120

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Brock, T.G., Nagaprakash, K., Margolis, D.I. et al. Modeling degranulation with liposomes: Effect of lipid composition on membrane fusion. J. Membarin Biol. 141, 139–148 (1994). https://doi.org/10.1007/BF00238247

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00238247

Key words

Navigation