Vesicular quantal size measured by amperometry at chromaffin, mast, pheochromocytoma, and pancreatic β-cells

Journal of Neurochemistry

Volumn 66, Issue 5, 1996, Pages 1914-1923

  Finnegan, Jennifer M ^a   Pihel, Karin ^a   Cahill, Paula S ^a   Huang, Lan ^b   Zerby, Susan E ^c   Ewing, Andrew G ^c   Kennedy, Robert T ^b   Wightman, R Mark ^a  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b University of Florida ^*  (United States)

^c PENNSYLVANIA STATE UNIVERSITY   (United States)

Author keywords

5 Hydroxytryptamine; Amperometry; Carbon fiber microelectrode; Catecholamine; Exocytosis; Insulin

Indexed keywords

CATECHOLAMINE; SEROTONIN;

AMPEROMETRY; ANIMAL CELL; ARTICLE; CALCIUM TRANSPORT; CELL VACUOLE; CHROMAFFIN CELL; ELECTROCHEMISTRY; EXOCYTOSIS; MAST CELL; NONHUMAN; PANCREAS ISLET BETA CELL; PHEOCHROMOCYTOMA CELL; PRIORITY JOURNAL; QUANTITATIVE ASSAY; SODIUM CALCIUM EXCHANGE;

ANIMALIA; COLEOPTERA; CURCULIONIDAE; SMICRONYX FULVUS;

EID: 0029874498     PISSN: 00223042     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1471-4159.1996.66051914.x     Document Type: Article

References (53)

1. Alvarez de Toledo G. and Fernandez J. M. (1990) Compound versus multigranular exocytosis in peritoneal mast cells. J. Gen. Physiol 95, 397-409.
2. Alvarez de Toledo G., Fernandez-Chacon R., and Fernandez J. M. (1993) Release of secretory products during transient vesicle fusion. Nature 363, 554-558.
3. Atkinson G., Ennis M., and Pearce F. L (1979) The effect of alkaline earth cations on the release of histamine from rat peritoneal mast cells treated with compound 48/80 and peptide 401. Br. J. Pharmacol. 65, 395-402.
4. Bekkers J. M., Richerson G. B., and Stevens C. F. (1990) Origin of variability in quantal size in cultured hippocampal neurons and hippocampal slices. Proc. Natl. Acad. Sci. USA 87, 5359-5362.
5. Boyd I. A. and Martin A. R. (1956) The end-plate potential in mammalian muscle. J. Physiol. (Lond.) 132, 74-91.
6. Burgoyne R. D. (1991) Control of exocytosis in adrenal chromaffin cells. Biochim. Biophys. Acta 1071, 174-202.
7. Cahill P. S. and Wightman R. M. (1995) Simultaneous amperometric measurement of ascorbate and catecholamine secretion from individual bovine adrenal medullary cells. Anal. Chem. 67, 2599-2605.
8. Caulfield J. P , el Lati S., Thomas G., and Church M. K. (1990) Dissociated human foreskin mast cells degranulate in response to anti-IgE and substance P. Lab. Invest. 63, 502-510.
9. Cheek T. R. and Barry V. A. (1993) Stimulus-secretion coupling in excitable cells: a central role for calcium. J. Exp. Biol. 184, 183-196.
10. Chen T. K., Luo G., and Ewing A. G. (1994) Amperometric monitoring of stimulated catecholamine release from rat pheochromocytoma (PC 12) cells at the zeptomole level. Anal. Chem. 66, 3031-3035.
11. Chow R. H., von Rüden L., and Neher E. (1992) Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells. Nature 356, 60-63.
12. Ciolkowski E. L., Maness K. M., Cahill P. S., Wightman R. M., Evans D. H., Fosset B., and Amatore C. (1994) Disproportionation during electrooxidation of catecholamines at carbon-fiber microelectrodes. Anal. Chem. 66, 3611-3617.
13. Colquhoun D. and Hawkes D. (1983) The principles of the stochastic interpretation of ion-channel mechanisms, in Single-Channel Recordings (Sakmann B. and Neher E., eds), pp. 135-174, Plenum Press, New York.
14. Corcoran J. J., Wilson S. P., and Kirshner N. (1984) Flux of catecholamines through chromaffin vesicles in cultured bovine adrenal medullary cells. J. Biol. Chem. 259, 6208-6214.
15. Coupland R. E. (1968) Determining sizes and distributions of sizes of spherical bodies such as chromaffin granules in tissue sections. Nature 217, 384-388.
16. 2+ at single bovine chromaffin cells. J. Biol. Chem. 270, 5353-5359.
17. Helander H. F. and Bloom G. D. (1974) Quantitative analysis of mast cell structure. J. Microsc. 100, 315-321.
18. Horrigan F. T. and Bookman R. J. (1994) Releasable pools and the kinetics of exocytosis in adrenal chromaffin cells. Neuron 13, 1119-1129.
19. Hutton J. C., Penn E. J., and Peshavaria M. (1983) Low molecular weight constituents of isolated insulin secretory granules: divalent cations, adenine nucleotides and inorganic phosphates. Biochem. J. 210, 297-305.
20. Jankowski J. A., Finnegan J. M., and Wightman R. M. (1994) Extracellular ionic composition alters kinetics of vesicular release of catecholamines and quantal size during exocytosis at adrenal medullary cells. J. Neurochem. 63, 1739-1747.
21. Kalina M., Grimelius L., Cedermark B., and Hammel I. (1989) Insulin and c-peptide co-localization in the beta granules of normal human pancreas and insulinomas. Virchows Arch. [A] 416, 19-23.
22. 2+ and short-term synaptic plasticity. Nature 371, 603-606.
23. Kawagoe K. T., Zimmerman J. B., and Wightman R. M. (1993) Principles of voltammetry and microelectrode surface states. J. Neurosci. Methods 48, 225-240.
24. Kennedy R. T., Huang L., Atkinson M. A., and Dush P. (1993) Amperometric monitoring of chemical secretions from individual pancreatic β-cells. Anal. Chem. 65, 1882-1887.
25. 2+ by isolated vesicles from adrenal medulla. Biochim. Biophys. Acta 691, 61-70.
26. Larsson L.-I., Sundler F., and Hakanson R. (1976) Pancreatic polypeptide - a postulated new hormone: identification of its cellular storage site by light and electron microscopic immunocytochemistry. Diabetologia 12, 211-226.
27. Laslop A., Mahata S K., Wolkersdorfer M., Mahata M., Srivastava M., Seidah N. G., Fisher-Colbrie R., and Winkler H. (1994) Large dense-core vesicles in rat adrenal after reserpine: levels of mRNAs of soluble and membrane-bound constituents in chromaffin and ganglion cells indicate a biosynthesis of vesicles with higher secretory quanta. J. Neurochem. 62, 2448-2456.
28. Leszczyszyn D. J., Jankowski J. A., Viveros O. H., Diliberto E. J. Jr., Near J. A., and Wightman R. M. (1991) Secretion of catecholamines from individual adrenal medullary cells. J. Neurochem. 56, 1855-1863.
29. Martin A. R. (1966) Quantal nature of synaptic transmission. Physiol. Rev. 46, 51-66.
30. Matsuda M., Okabe T., Sugimoto N., Senda T., and Fujita H. (1994) Tetanus toxin and Clostridium perfringens enterotoxin as tools for the study of exocytosis. Ann. NY Acad. Sci. 710, 94-106.
31. Monck J. and Fernandez J. M. (1994) The exocytotic fusion pore and neurotransmitter release. Neuron 12, 707-716.
32. Moro M. A., Lopez M. G., Gandia L., Michelena P., and Garcia A. G. (1990) Separation and culture of living adrenaline-containing and noradrenaline-containing cells from bovine adrenal medullae. Anal. Biochem. 185, 243-248.
33. Ornberg R. L., Furuya S., Goping G., and Kuijpers G. A. J. (1995) Granule swelling in stimulated bovine adrenal chromaffin cells: regulation by internal granule pH. Cell Tissue Res. 279, 85-92.
34. Paras C. D. and Kennedy R. T. (1995) Electrochemical detection of exocytosis at single rat melanotrophs. Anal. Chem. 67, 3633-3637.
35. Pieribone V. A., Shupliakov O., Brodin L., Hilfiker-Rothenfiuh S., Czernik A. J., and Greengard P. (1995) Distinct pools of synaptic vesicles in neurotransmitter release. Nature 375, 493-496.
36. Pihel K., Hsieh S., Jorgenson J. W., and Wightman R. M. (1995) Electrochemical detection of histamine and 5-hydroxytryptamine at isolated mast cells. Anal. Chem. 67, 4514-4521.
37. Pollard H. B., Ornberg R., Levine M., Keiner K., Morita K., Levine R., Forsberg E., Brocklehurst K. W., Duong L., Lelkes P. I., Heldman E., and Youdim M. (1985) Hormone secretion by exocytosis with emphasis on information from the chromaffin cell system. Vitam. Horm. 42, 109-196.
38. Robinson I. M., Finnegan J. M., Monck J. R., Wightman R. M., and Fernandez J. M. (1995) Colocalization of calcium entry and exocytotic release sites in adrenal chromaffin cells. Proc. Natl Acad. Sci. USA 92, 2474-2478.
39. Rohlf F. J. and Sokal R. R. (1981) Critical values for correlation coefficients, in Statistical Tables, p. 168. W. H. Freeman and Co., New York.
40. Scepek S. and Lindau M. (1993) Focal exocytosis by eosinophil-compound exocytosis and cumulative fusion. EMBO J. 12, 1811-1817.
41. Schroeder T. J., Jankowski J. A., Kawagoe K. T., Wightman R. M., Lefrou C., and Amatore C. (1992) Analysis of diffusional broadening of vesicular packets of catecholamine released from biological cells during exocytosis. Anal. Chem. 64, 3077-3083.
42. Schubert D., LaCorbiere M., Klier F. G., and Steinbach J. H. (1980) The modulation of neurotransmitter synthesis by steroid hormones and insulin. Brain Res. 190, 67-79.
43. Sokal R. R. and Rohlf F. J. (1981) Significance tests in correlation. in Biometry, p. 583. W. H. Freeman and Co., New York.
44. Sulzer D., Maidment N. T., and Rayport S. (1993) Amphetamine and other weak bases act to promote reverse transport of dopamine in ventral midbrain neurons. J. Neurochem. 60, 527-535.
45. Sulzer D., Chen T. K., Lau Y. Y., Kristensen H., Rayport S., and Ewing A. (1995) Amphetamine redistributes dopamine from synaptic vesicles to the cytosol and promotes reverse transport. J. Neurosci. 15, 4102-4108.
46. Viveros O. H., Arqueros L., and Kirshner N. (1969) Quantal secretion from the adrenal medulla all-or-none release of storage vesicle content. Science 165, 911-913.
47. von Rüden L. and Neher E. (1993) A Ca-dependent early step in the release of catecholamines from adrenal chromaffin cells. Science 262, 1061-1065.
48. Waymire J. C., Haycock J. W., and George R. J. (1984) Stimulation-dependent regulation of catecholamine biosynthesis in purified adrenal chromaffin cells: phosphorylation and activation of tyrosine hydroxylase, in Catecholamines: Basic and Peripheral Mechanisms (Usdin E., Carlsson A., Dahlstrom A., and Engel J., eds), pp. 195-202. Alan R. Liss, New York.
49. Wightman R. M., Jankowski J. A., Kennedy R. T., Kawagoe K. T., Schroeder T. J., Leszczyszyn D. J., Near J. A., Diliberto E. J. Jr., and Viveros O. H. (1991) Temporally resolved catecholamine spikes correspond to single vesicle release from individual chromaffin cells. Proc. Natl. Acad. Sci. USA 88, 10754-10758.
50. Wightman R. M., Schroeder T. J., Finnegan J. M., Ciolkowski E. L., and Pihel K. (1995) Time course of release of catecholamines from individual vesicles during exocytosis at adrenal medullary cells. Biophys. J. 68, 383-390
51. Wilson S. P. and Viveros O. H. (1981) Primary culture of adrenal medullary chromaffin cells in a chemically defined medium. Exp. Cell Res. 133, 159-169.
52. Winkler H., Apps D. K., and Fischer-Colbrie R. (1986) The molecular function of adrenal chromaffin granules: established facts and unresolved topics. Neuroscience 18, 261-290.
53. 2+ on monomer-dimer and monomer-tetramer equilibria of chromogranin A. J. Biol. Chem. 267, 11236-11241.