Exocytosis in excitable cells: A conserved molecular machinery from yeast to neuron

European Journal of Endocrinology

Volumn 137, Issue 1, 1997, Pages 1-9

  Lledo, Pierre Marie ^a,b  

^a CNRS   (France)

^b UNIVERSITÉ PARIS SACLAY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HORMONE; NEUROTRANSMITTER;

CELL GRANULE; CELL ORGANELLE; CELL POLARITY; CELL VACUOLE; ENDOCRINE CELL; EXOCYTOSIS; HORMONE RELEASE; HUMAN; MEMBRANE VESICLE; NERVE CELL EXCITABILITY; NERVE CELL PLASTICITY; NEUROTRANSMITTER RELEASE; NONHUMAN; PRIORITY JOURNAL; REVIEW; SACCHAROMYCES CEREVISIAE; YEAST;

ANIMALS; CALCIUM; EXOCYTOSIS; GTP-BINDING PROTEINS; HORMONES; NEURONS; NEUROTRANSMITTER AGENTS; SACCHAROMYCES CEREVISIAE;

EID: 0030845041     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1370001     Document Type: Review

References (55)

1. Pryer NK, Wuestehube LJ & Sheckman R. Vesicle-mediated protein sorting. Annual Review in Biochemistry 1992 61 471-516.
2. Rothman JE & Warren G. Implications of the SNARE hypothesis for intracellular membrane topology and dynamics. Current Biology 1994 4 220-233.
3. Douglas WW. Stimulus-secretion coupling: The concept and clues from chromaffin and other cells. British Journal of Pharmacology 1968 34 451-474.
4. Jahn R & De Camilla P. Membrane proteins of synaptic vesicles: Markers for neurons and neuroendocrine cells tools for the study of neurosecretion. In Markers for Neurons and Neuroendocrine Cells. Molecular and Cell Biology, Diagnostic Applications, edn 1, pp 25-92. Eds M Gratzl & K Eangley. Weinheim: VCH-Verlagsgesellschaft, 1991.
5. Südhof TC & Jahn R. Proteins of synaptic vesicles involved in exocytosis and membrane recycling. Neuron 1991 6 665-677.
6. Somogyi P, Hodgson AJ, DePotter RW, Fischer-Colbrie R, Schober M, Winkler H et al. Chromogranin immunoreactivity in the central nervous system. Immunochemical characterization, distribution and relationship to catecholamine and enkephalin pathways. Brain Research Reviews 1984 8 193-230.
7. Gratzl M & Langley OK (Eds). Markers for Neurons and Neuroendocrine Cells. Molecular and Cell Biology, Diagnostic Applications, edn 1. Weinheim: VCH-Verlagsgesellschaft, 1991.
8. Bennett MK & Scheller RH. The molecular machinery for secretion is conserved from yeast to neurons. Proceedings of the National Academy of Sciences of the USA 1993 90 2559-2563.
9. Kelly RB. Storage and release of neurotransmitters. Cell/Neuron (Suppl) 1993 72 43-53.
10. +-ATPase of mammalian synaptic vesicles. Journal of Neurochemistry 1990 55 1663-1670.
11. Tabb JS, Kish PE, Van Dyke R & Ueda T. Glutamate transport into synaptic vesicles: Roles of membrane potential, pH gradient and intravesicular pH. Journal of Biological Chemistry 1992 267 15412-15418.
12. Baker PF & Knight DE. Calcium-dependent exocytosis in bovine adrenal medullary cells with leaky plasma membranes. Nature 1978 276 620-622.
13. Gomperts BD & Fernandez JM. Technique for membrane permeabilization. Trends in Biochemical Science 1985 10 414-417.
14. Peng YY & Zucker RS. Release of LHRH is linearly related to the time integral of presynaptic calcium elevation above a threshold level in bullfrog sympathetic ganglia. Neuron 1993 10 465-473.
15. Neher E & Zucker R. Multiple calcium-dependent processes related to secretion in bovine chromaffin cells. Neuron 1993 10 21-30.
16. Thomas P, Wong JG & Almers W. Millisecond studies of secretion in single rat pituitary cells stimulated by flash photolysis of caged calcium. EMBO Journal 1993 12 303-306.
17. Rothman JE. Mechanisms of intracellular protein transport. Nature 1994 372 55-63.
18. Galli T, Garcia EP, Mundigl O, Chilcote TJ & De Camelli P. V- and T-SNAREs in neuronal exocytosis: a need for additional components to define sites of release. Neuropharmacology 1995 34 1351-1360.
19. Calakos N & Scheller RH. Synaptic vesicle biogenesis, docking, and fusion: a molecular description. Physiological Reviews 1996 76 1-29.
20. Chapman ER, Hanson PI & Jahn R. The neuronal exocytotic fusion machine: some new developments. Neuropharmacology 1995 34 1343-1349.
21. Rothman JE & Wieland FT. Protein sorting by transport vesicles. Science 1996 272 227-234.
22. Marty A & Neher E. Tight seal whole-cell recording. In Single-Channel Recording, pp 107-121. Eds B Sakmann & E Neher. New York: Plenum Press, 1983.
23. Fernandez JM, Bezanilla F & Taylor RE. Distribution and kinetics of membrane dielectric polarization. Journal of Genetics and Physiology 1982 79 41-67.
24. Lindau M & Neher E. Patch-clamp techniques for time-resolved capacitance measurements in single cells. Pflügers Archives of Genetics and Physiology 1988 411 137-146.
25. Neher E & Marty A. Discrete changes of cell membrane capacitance observed under conditions of enhanced secretion in bovine adrenal chromaffin cells. Proceedings of the National Academy of Sciences of the USA 1982 79 6712-6716.
26. Zorec R, Henigman F, Mason WT & Kordas M. Electrophysiological study of hormone secretion by single adenohypophyseal cells. Methods in Neuroscience 1991 4 194-210.
27. Lledo P-M, Johannes L, Vernier P, Zorec R, Darchen F, Vincent J-D et al. Rab3 proteins: key players in the control of exocytosis. Trends in Neurosciences 1994 17 426-432.
28. Matthews G. Synaptic exocytosis and endocytosis: capacitance measurements. Current Opinion in Neurobiology 1996 6 358-364.
29. Henkel AW & Almers W. Fast steps in exocytosis and endocytosis studied by capacitance measurements in endocrine cells. Current Opinion in Neurobiology 1996 6 350-357.
30. Taraskevich PS & Douglas WW. Electrical activity in adenohypophyseal cells and effects of hypophyseotropic substances. Federation Proceedings. Federation of American Societies for Experimental Biology 1984 43 2373-2378.
31. Tse FW, Tse A & Hille B. Cyclic calcium changes in intracellular stores of gonadotropes during gonadotropin-releasing hormone-stimulated calcium oscillations. Proceedings of the National Academy of Sciences of the USA 1994 91 9750-9754.
32. Sikdar SK, Zorec R & Mason WT. cAMP directly facilitates calcium-induced exocytosis in bovine lactotrophs. FEBS Letters 1990 273 150-154.
33. Sikdar SK, Zorec R, Brown D & Mason WT. Dual effects of G-protein activation on calcium-dependent exocytosis in bovine lactotrophs. FEBS Letters 1989 253 88-92.
34. Bean BP. Classes of calcium channels in vertebrate cells. Annual Review of Physiology 1989 51 367-384.
35. Llinas R, Sugimori M & Silver RB. The concept of calcium concentration microdomains in synaptic transmission. Neuropharmacology 1995 34 1443-1452.
36. Sabatini BL & Regehr WG. Detecting changes in calcium influx which contribute to synaptic modulation in mammalian brain slice. Neuropharmacology 1995 34 1453-1467.
37. Burgoyne RD & Morgan A. Calcium and secretory-vesicle dynamics. Trends in Neurosciences 1995 18 191-196.
38. Sheng Z-H, Rettig J, Cook T & Catterall WA. Calcium-dependent interaction of N-type calcium channels with the synaptic core complex. Nature 1996 379 451-454.
39. Südhof TC. The synaptic vesicle cycle: a cascade of protein-protein interactions. Nature 1995 375 645-653.
40. Salminen A & Novick PJ. A ras-like protein is required for a post-Golgi event in yeast secretion. Cell 1987 47 527-538.
41. Valencia A, Chardin P, Wittinghofer A & Sander C. The ras protein family: evolutionary tree and role of conserved amino acids. Biochemistry 1991 30 4637-4648.
42. Pfeffer SR. GTP-binding proteins in intracellular transport. Trends in Cell Biology 1992 2 41-46.
43. Grand RJ & Owen D. The biochemistry of ras p21. Biochemical Journal 1991 279 609-631.
44. Chavrier P, Gorvel JP, Stelzer E, Simons K, Gruenberg J & Zerial M. Hypervariable C-terminal domain of rab proteins acts as a targeting signal. Nature 1991 353 769-772.
45. Musha T, Kawata M & Takai Y. The geranylgeranyl moiety but not the methyl moiety of the smg-25A/rab3A protein is essential for the interaction with membrane and its inhibitory GDP/GTP exchange protein. Journal of Biological Chemistry 1992 267 9821-9825.
46. Stettler O, Nothias F, Tavitian B & Vernier P. Double in situ hybridization reveals overlapping neuronal populations expressing the low molecular weight GTPases Rab3a and Rab3b in rat brain. European Journal of Neurosciences 1995 7 702-713.
47. Mizoguchi A, Kim S, Ueda T, Kikuchi A, Yorifuji H, Hirokawa N et al. Localization and subcellular distribution of smg p25A, a ras p21-like GTP-binding protein, in rat brain. Journal of Biological Chemistry 1990 265 11872-11879.
48. Darchen F, Zahraoui A, Hammel F, Monteils M-P, Tavitian A & Scherman U. Association of the GTP-binding protein Rab3A with bovine adrenal chromaffin granules. Proceedings of the National Academy of Sciences of the USA 1990 87 5692-5696.
49. Fischer von Mollard G, Südhof TC & Jahn R. A small GTP-binding protein dissociates from synaptic vesicles during exocytosis. Nature 1991 349 79-81.
50. Oberhauser AF, Monck JR, Balch WE & Fernandez JM. Exocytotic fusion is activated by Rab3A peptides. Nature 1992 360 270-273.
51. Touchot N, Chardin P & Tavitian A. Four additional members of the ras gene superfamily isolated by an oligonucleotide strategy: molecular cloning of YPT-related cDNAs from a rat brain library. Proceedings of the National Academy of Sciences of the USA 1987 84 8210-8214.
52. Matsui Y, Kikuchi A, Kondo J, Hishida T, Teranishi Y & Takai Y. Nucleotide and deduced amino acid sequences of a GTP-binding protein family with molecular weights of 25 000 from bovine brain. Journal of Biological Chemistry 1988 263 11071-11074.
53. Lledo P-M, Vernier P, Vincent J-D, Mason WT & Zorec R. Inhibition of Rab3 expression attenuates calcium-dependent exocytosis in rat anterior pituitary cells. Nature 1993 364 540-544.
54. Melançon P. G whizz. Current Biology 1993 3 230-233.
55. Burgoyne RD & Morgan A. Regulated exocytosis. Biochemical Journal 1993 293 305-316.