The exocytotic fusion pore interface: a model of the site of neurotransmitter release

References

• Aimers W., Tse F. W. Transmitter release from synapses: does a preassembled fusion pore initiate exocytosis. Neuron 1990; 4: 813–818
   PubMedGoogle Scholar
• Alvarez de Toledo G., Fernandez J. M. The events leading to secretory granule fusion. Cell Physiology of Blood. Rockefeller University Press. 1988; 334–344
   Google Scholar
• Alvarez de Toledo G., Fernandez-Chacon R., Fernandez J. M. Release of secretory products during transient vesicle fusion. Nature 1993; 363: 554–557
   PubMed Web of Science ®Google Scholar
• Breckenridge L. J., Aimers W. Currents through the fusion pore that forms during exocytosis of a secretory vesicle. Nature 1987a; 328: 814–817
   PubMed Web of Science ®Google Scholar
• Breckenridge L. J., Aimers W. Final steps in ecocytosis observed in a cell with giant secretory granules. Proceedings of the National Academy of Sciences, USA 1987b; 84: 1945–1949
   PubMed Web of Science ®Google Scholar
• Chandler D. E., Heuser J. E. Arrest of membrane fusion events in mast cells by quick-freezing. Journal of Cell Biology 1980; 86: 666–674
   PubMedGoogle Scholar
• Chernomordik L. V., Melikyan G. B., Chizmadzhev Y. A. Biomembrane fusion: a new concept derived from model studies using two interacting planar lipid bilayers. Biochimica et Biophysica Acta 1987; 906: 309–352
   PubMed Web of Science ®Google Scholar
• Fernandez J. M., Neher E., Gomperts B. D. Capacitance measurements reveal stepwise fusion events in degranulating mast cells. Nature 1984; 312: 453–455
   PubMed Web of Science ®Google Scholar
• Gruner S. M. Intrinsic curvature hypothesis for biomembrane lipid composition: a role for nonbilayer lipids. Proceedings of the National Academy of Sciences, USA 1985; 82: 3665–3669
   PubMed Web of Science ®Google Scholar
• Helfrich W. Elastic properties of lipid bilayers: theory and possible experiments. Zeitschrift fuer Naturforschung, Section C 1973; 28: 693–703
   PubMed Web of Science ®Google Scholar
• Helm C. A., Israelachvili J. N. Forces between phospholipid bilayers and relationship to membrane fusion. Methods in Enzymology 1993; 220: 130–143
   PubMedGoogle Scholar
• Helm C. A., Israelachvili J. N., McGuiggan P. M. Molecular mechanisms and forces involved in the adhesion and fusion of amphiphilic bilayers. Science 1989; 246: 919–922
   PubMed Web of Science ®Google Scholar
• Helm C. A., Israelachvili J. N., McGuiggan P. M. Role of hydrophobic forces in bilayer adhesion and fusion. Biochemistry 1992; 31: 1794–1805
   PubMed Web of Science ®Google Scholar
• Heuser J. E., Reese T. S. Structural changes after transmitter release at the frog neuromuscular junction. Journal of Cell Biology 1981; 88: 564–580
   PubMedGoogle Scholar
• Hoffmann W., Sarzala M. G., Gomez-Fernandez J. C., Goni F. M., Restall C. J., Chapman D. Protein rotational diffusion and lipid structure of reconstituted systems of Ca2+-activated adenosine triphosphatase. Journal of Molecular Biology 1980; 141: 119–132
   PubMedGoogle Scholar
• Kemble G. W., Danieli T., White J. M. Lipid-anchored influenza hemagglutinin promotes hemifusion, not complete fusion. Cell 1994; 76: 383–391
   PubMed Web of Science ®Google Scholar
• Knoll G., Braun C., Plattner H. Quenced flow analysis of exocytosis in Paramecium cells: time course, changes in membrane structure, and calcium requirements revealed after rapid mixing and rapid freezing of intact cells. Journal of Cell Biology 1991; 113: 1295–1304
   PubMedGoogle Scholar
• Kozlov M. M., Leikin S. L., Chernomordik L. V., Markin V. S., Chizmadzhev Y. A. Stalk mechanism of vesicle fusion. Intermixing of aqueous contents. European Biophysics Journal 1989; 17: 121–129
   PubMed Web of Science ®Google Scholar
• Leckband D. E., Helm C. A., Israelachvili J. N. Rote of calcium in the adhesion and fusion of bilayers. Biochemistry 1993; 32: 1127–1140
   PubMedGoogle Scholar
• Lindau M., Nusse O., Bennett J., Cromwell O. The membrane fusion events in degranulating guiea pig eosinophils. Journal of Cell Science 1993; 104: 203–209
   PubMedGoogle Scholar
• Krasne S., Eisenman G., Szabo G. Freezing and melting of lipid bilayers and the mode of action of nonactin, valinomycin, and gramicidin. Science 1971; 174: 412–415
   PubMed Web of Science ®Google Scholar
• Markin V. S., Kozlov M. M., Borovjagin V. L. On the theory of membrane fusion. The stalk mechanism. General Physiology and Biophysics 1984; 5: 361–377
   Google Scholar
• Monck J. R., Fernandez J. M. The exocytotic fusion pore. Journal of Cell Biology 1992; 119: 1395–1404
   PubMed Web of Science ®Google Scholar
• Monck J. R., Fernandez J. M. The exocytotic fusion pore and neurotransmitter release. Neuron 1994; 12: 707–716
   PubMed Web of Science ®Google Scholar
• Monck Ft J., Alvarez de Toledo G., Fernadez J. M. Tension in secretory granule membranes causes extensive membrane transfer through the exocytotic fusion pore. Proceedings of the National Academy of Sciences, USA 1990; 87: 7804–7808
   PubMedGoogle Scholar
• Monck J. R., Oberhauser A. F., Alvarez deToledo G., Fernandez J. M. Is swelling of the secretory granule matrix the force that dilates the exocytotic fusion pore. Biophysical Journal 1991a; 59: 39–47
   PubMedGoogle Scholar
• Monck J. R., Oberhauser A. F., Alvarez de Toledo G., Fernandez J. M. Tension in secretory granule membrane transfer through the exocytotic fusion pore. Biophysical Journal 1991b; 59: 207a
   Google Scholar
• Nakata T., Hirokawa N. Organization of cortical cytoskeleton of cultured chromaffin cells and involvement in secretion as revealed by quick-freeze, deep-etching and double-label and immunoelectron microscopy. Journal of Neuroscience 1991; 12: 2186–2197
   Google Scholar
• Nanavati C., Fernandez J. M. The secretory granule matrix: a fast-acting smart polymer. Science 1993; 259: 963–965
   PubMed Web of Science ®Google Scholar
• Nanavati C., Markin V. S., Oberhauser A., Fernandez J. M. The exocytotic fusion pore modeled as a lipidic pore. Biophysical Journal 1992; 63: 1118–1132
   PubMed Web of Science ®Google Scholar
• Oberhauser A. F., Fernandez J. M. Patch-clamp studies of intact secretory granules. Biophysical Journal 1993; 65: 1844–1852
   PubMedGoogle Scholar
• Oberhauser A. F., Monck J. R., Fernandez J. M. Events leading to the opening and closing of the exocytotic fusion pore have markedly different temperaturre dependencies. Kinetic analysis of single fusion events in patch-clamped mouse mast cells. Biophysical Journal 1992a; 61: 800–809
   PubMedGoogle Scholar
• Ohki S. Surface tension, hydration energy and membrane fusion. Molecular Mechanisms of Membrane Fusion, S. Ohki, D. Doyle, T. D. Flanagan, S. Withers, E. Mayhew. Plenum Press, New York 1987; 123–137
   Google Scholar
• Ornberg R. L., Reese T. S. Beginning of exocytosis captured by rapid-freezing of Limulus amebocytes. Journal of Cell Biology 1981; 90: 40–54
   PubMedGoogle Scholar
• Pollard H. B., Rojas E., Pastor R. W., Rojas E. M., Guy H. R., Burns A. L. Synexin: molecular mechanism of calcium-dependent membrane fusion and voltage-dependent calcium-channel activity. Annals of the New York Academy of Sciences 1991; 635: 328–351
   PubMedGoogle Scholar
• Rand R. P. Interacting phospholipid bilayers: measured forces and induced structural changes. Annual Reviews of Biophysics and Bioengineering 1981; 10: 277–314
   PubMedGoogle Scholar
• Rothman J. E., Orci L. Molecular dissection of the secretory pathway. Nature 1992; 355: 409–415
   PubMed Web of Science ®Google Scholar
• Schmidt W., Patzak A., Lingg G., Winkler H. Membrane events in adrenal chromaffin cells during exocytosis: a freeze-etching analysis after rapid cryofixation. European Journal of Cell Biology 1983; 32: 31–37
   PubMedGoogle Scholar
• Song L., Ahkong Q. F., Georgescauld D., Lucy J. A. Membrane fusion without cytoplasmic fusion (hemi-fusion) in erythrocytes that are subjected to electrical breakdown. Biochima et Biophysica Acta 1991; 106: 554–62
   Google Scholar
• Spruce A. E., Breckenridge L. J., Lee A. K., Aimers W. Properties of the fusion pore that forms during exocytosis of a mast cell secretory vesicle. Neuron 1990; 4: 643–654
   PubMed Web of Science ®Google Scholar
• Sudhof T. C., Jahn R. Proteins of synaptic vesicles involved in exocytosis and membrane recycling. Neuron 1991; 6: 665–677
   PubMed Web of Science ®Google Scholar
• Thomas L., Hartung K., Langosch D., Rehm H., Banberg E., Franke W. W., Betz H. Identification of synaptophysin as a hexameric channel protein of the synaptic vesicle membrane. Science 1988; 242: 1050–1053
   PubMed Web of Science ®Google Scholar
• Verdugo P. Mucin exocytosis. American Review of Respiratory Disease 1991; 144: S33–S37
   Google Scholar
• Volknandt W., Zimmermann H. Acetylcholine, ATP, and proteoglycan are common to synaptic vesicles isolated from the electric organs of electric ell and electric catfish as well as from rat diaphragm. Journal of Neurochemistry 1986; 47: 1449–1462
   PubMed Web of Science ®Google Scholar
• White J. M. Membrane fusion. Science 1992; 258: 917–924
   PubMed Web of Science ®Google Scholar
• Zimmerberg J., Curran M., Cohen F. S., Brodwick M. Simultaneous electrical and optical measurements show that membrane fusion precedes secretory granule swelling during exocytosis of beige mouse mast cells. Proceedings of the National Academy of Sciences, USA 1987; 84: 1585–1589
   PubMed Web of Science ®Google Scholar