Extrasynaptic release of dopamine in a retinal neuron: Activity dependence and transmitter modulation

Neuron

Volumn 30, Issue 1, 2001, Pages 211-225

  Puopolo, Michelino ^a   Hochstetler, Spencer E ^b   Gustincich, Stefano ^a   Wightman, R Mark ^b   Raviola, Elio ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

^b University of North Carolina at Chapel Hill   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; COMPLEMENTARY DNA; DOPAMINE; DOPAMINE 2 RECEPTOR; KAINIC ACID; QUINPIROLE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DOPAMINE RELEASE; DOPAMINERGIC NERVE CELL; EXOCYTOSIS; EXTRACELLULAR FLUID; IMMUNOCYTOCHEMISTRY; MOUSE; NERVE POTENTIAL; NONHUMAN; PRESYNAPTIC NERVE; PRIORITY JOURNAL; RETINA NERVE CELL; SURFACE PROPERTY;

EID: 0035041303     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0896-6273(01)00274-4     Document Type: Article

References (58)

1. Albillos A., Dernick G., Horstmann H., Almers W., Alvarez de Toledo G., Lindau M. The exocytotic event in chromaffin cells revealed by patch amperometry. Nature. 389:1997;509-512.
2. Bean B.P., Mintz I.M. Pharmacology of different types of calcium channels in rat neurons. Peracchia C. Handbook of Membrane Channels. Molecular and Cellular Physiology:1994;199-210 Academic Press, San Diego, CA.
3. Bekkers J.M., Richerson G.B., Stevens C.F. Origin of variability in quantal size in cultured hippocampal neurons and hippocampal slices. Proc. Natl. Acad. Sci. USA. 87:1990;5359-5362.
4. Bjelke B., Goldstein M., Tinner B., Andersson C., Sesack S.R., Steinbusch H.W.M., Lew J.Y., He X., Watson S., Tengroth B., Fuxe K. Dopaminergic transmission in the rat retina. evidence for volume transmission J. Chem. Neuroanatomy. 12:1996;37-50.
5. Brandstätter J.H., Wässle H., Betz H., Morgans C.W. The plasma membrane protein SNAP-25, but not syntaxin, is present at photoreceptor and bipolar cell synapses in the rat retina. Eur. J. Neurosci. 8:1996;823-828.
6. Bruns D., Jahn R. Real-time measurement of transmitter release from single synaptic vesicles. Nature. 377:1995;62-65.
7. Bunin M.A., Wightman R.M. Paracrine neurotransmission in the CNS by 5-hydroxytryptamine. Trends Neurosci. 22:1999;377-382.
8. B receptors J. Neurophysiol. 74:1995;1137-1148.
9. Cheramy A., Leviel V., Glowinski J. Dendritic release of dopamine in the substantia nigra. Nature. 289:1981;537-542.
10. Chow R.H., von Rüden L., Neher E. Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells. Nature. 356:1992;60-63.
11. Chow R.H., Klingauf J., Heinemann C., Zucker R.S., Neher E. Mechanisms determining the time course of secretion in neuroendocrine cells. Neuron. 16:1996;369-376.
12. Dan Y., Song H.-J., Poo M.-M. Evoked neuronal secretion of false transmitters. Neuron. 13:1994;909-917.
13. De Waele P., De Groote G., Van De Voorde A., Fiers W., Franssen J.-D., Herion P., Urbain J. Isolation and identification of monoclonal antibodies directed against human placental alkaline phosphatase. Arch. Int. Physiol. Biochim. 90:1982;B21.
14. 2 receptor subfamily in rat retina. ultrastructural immunogold and in situ hybridization studies Eur. J. Neurosci. 11:1999;1391-1402.
15. Duchen M.R. Fluorescence-monitoring cell chemistry in vivo. Stamford J.A. Monitoring Neuronal Activity. A Practical Approach:1992;Oxford University Press, New York. 231-260.pp.
16. Feigenspan A., Gustincich S., Bean B.P., Raviola E. Spontaneous activity of solitary dopaminergic cells of the retina. J. Neurosci. 18:1998;6776-6789.
17. Finnegan J.M., Pihel K., Cahill P.S., Huang L., Zerby S.E., Ewing A.G., Kennedy R.T., Wightman R.M. Vesicular quantal size measured by amperometry at chromaffin, mast, pheochromocytoma, and pancreatic β-cells. J. Neurochem. 66:1996;1914-1923.
18. Galli A., Blakely R.D., DeFelice L.J. Patch-clamp and amperometric recordings from norepinephrine transporters. channel activity and voltage-dependent uptake Proc. Natl. Acad. Sci. USA. 95:1998;13260-13265.
19. Garaschuk O., Yaari Y., Konnerth A. Release and sequestration of calcium by ryanodine-sensitive stores in rat hippocampal neurones. J. Physiol. 502:1997;13-30.
20. Glitsch M., Llano I., Marty A. Glutamate as a candidate retrograde messenger at interneurone-Purkinje cell synapses of rat cerebellum. J. Physiol. 497:1996;531-537.
21. Grace A.A., Bunney B.S. Intracellular and extracellular electrophysiology of nigral dopaminergic neurons - 1. Identification and characterization. Neuroscience. 10:1983;301-315. a.
22. Grace A.A., Bunney B.S. Intracellular and extracellular electrophysiology of nigral dopaminergic neurons - 2. Action potential generating mechanisms and morphological correlates. Neuroscience. 10:1983;317-331. b.
23. 2+ indicators with greatly improved fluorescence properties. J. Biol. Chem. 260:1985;3440-3450.
24. Gustincich S., Feigenspan A., Wu D.-K., Koopman L.J., Raviola E. Control of dopamine release in the retina. a transgenic approach to neural networks Neuron. 18:1997;723-736.
25. A receptors of retinal dopaminergic neurons. J. Neurosci. 19:1999;7812-7822.
26. Hochstetler S.E., Wightman R.M. Detection of secretion by electrochemical methods. Bloomfield V., De Felice L. On-Line Biophysics Textbook. 1998;Biophysical Society, Bethesda, MD, http://biosci.umn.edu/biophys/OLTB/Textbook.html.
27. Hochstetler S.E., Puopolo M., Gustincich S., Raviola E., Wightman R.M. Real-time amperometric measurements of zeptomole quantities of dopamine released from neurons. Anal. Chem. 72:2000;489-496.
28. 2+-dependent exocytosis in the somata of dorsal root ganglion neurons. Neuron. 17:1996;135-145.
29. Jaffe E.H., Marty A., Schulte A., Chow R.H. Extrasynaptic vesicular transmitter release from the somata of substantia nigra neurons in rat midbrain slices. J. Neurosci. 18:1998;3548-3553.
30. Kawagoe K.T., Zimmerman J.B., Wightman R.M. Principles of voltammetry and microelectrode surface states. J. Neurosci. Methods. 48:1993;225-240.
31. Kim K.-T., Koh D.-S., Hille B. Loading of oxidizable transmitters into secretory vesicles permits carbon-fiber amperometry. J. Neurosci. 20:2000;1-5. RC101.
32. Koh D.-S., Hille B. Modulation by neurotransmitters of catecholamine secretion from sympathetic ganglion neurons detected by amperometry. Proc. Natl. Acad. Sci. USA. 94:1997;1506-1511.
33. Kolb H., Cuenca N., Wang H.-H., Dekorver L. The synaptic organization of the dopaminergic amacrine cell in the cat retina. J. Neurocytol. 19:1990;343-366.
34. Kolb H., Cuenca N., Dekorver L. Postembedding immunocytochemistry for GABA and glycine reveals the synaptic relationships of the dopaminergic amacrine cell of the cat retina. J. Comp. Neurol. 310:1991;267-284.
35. Kombian S.B., Mouginot D., Pittman Q.J. Dendritically released peptides act as retrograde modulators of afferent excitation in the supraoptic nucleus in vitro. Neuron. 19:1997;903-912.
36. Aergic transmission in hippocampal CA1. J. Neurophysiol. 82:1999;2556-2564.
37. Nguyen-Legros J. Morphology and distribution of catecholamine-neurons in mammalian retina. Progr. Retinal Res. 7:1988;113-147.
38. Nirenberg M.J., Chan J., Liu Y., Edwards R.H., Pickel V.M. Ultrastructural localization of the vesicular monoamine transporter-2 in midbrain dopaminergic neurons. potential sites for somatodendritic storage and release of dopamine J. Neurosci. 16:1996;4135-4145.
39. Pothos E., Desmond M., Sulzer D. L-3,4-dihydroxyphenylalanine increases the quantal size of exocytotic dopamine release in vitro. J. Neurochem. 66:1996;629-636.
40. Pothos E.N., Davila V., Sulzer D. Presynaptic recording of quanta from midbrain dopamine neurons and modulation of the quantal size. J. Neurosci. 18:1998;4106-4118.
41. Sandell J.H., Masland R.H. A system of indoleamine-accumulating neurons in the rabbit retina. J. Neurosci. 6:1986;3331-3347.
42. Simmons M.L., Terman G.W., Gibbs S.M., Chavkin C. L-type calcium channels mediate dynorphin neuropeptide release from dendrites but not axons of hippocampal granule cells. Neuron. 14:1995;1265-1272.
43. Stevens C.F., Tsujimoto T. Estimates for the pool size of releasable quanta at a single central synapse and for the time required to refill the pool. Proc. Natl. Acad. Sci. USA. 92:1995;846-849.
44. Steyer J.A., Horstmann H., Almers W. Transport, docking and exocytosis of single secretory granules in live chromaffin cells. Nature. 388:1997;474-478.
45. Tauchi M., Madigan N.K., Masland R.H. Shapes and distributions of the catecholamine-accumulating neurons in the rabbit retina. J. Comp. Neurol. 293:1990;178-189.
46. Trifaró J.-M., Glavinovic M., Rosé S.D. Secretory vesicle pools and rate and kinetics of single vesicle exocytosis in neurosecretory cells. Neurochem. Res. 22:1997;831-841.
47. 2+ entry and quantal dopamine secretion in carotid body glomus cells. Proc. Natl. Acad. Sci. USA. 91:1994;10208-10211.
48. Verkhratsky A., Shmigol A. Calcium-induced calcium release in neurones. Cell Calcium. 19:1996;1-14.
49. Veruki M.L. Dopaminergic neurons in the rat retina express dopamine D2/3 receptors. Eur. J. Neurosci. 9:1997;1096-1100.
50. 1 receptors in rat retina. Eur. J. Neurosci. 8:1996;2286-2297.
51. Wässle H., Chun M.H. Dopaminergic and indoleamine-accumulating amacrine cells express GABA-like immunoreactivity in the cat retina. J. Neurosci. 8:1988;3383-3394.
52. 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., Viveros O.H. Temporally resolved catecholamine spikes correspond to single vesicle release from individual chromaffin cells. Proc. Natl. Acad. Sci. USA. 88:1991;10754-10758.
53. Wightman R.M., Schroeder T.J., Finnegan J.M., Ciolkowski E.L., Pihel K. Time course of release of catecholamines from individual vesicles during exocytosis at adrenal medullary cells. Biophys. J. 68:1995;383-390.
54. Witkovsky P., Dearry A. Functional roles of dopamine in the vertebrate retina. Progr. Retinal Res. 11:1991;247-292.
55. Witkovsky P., Nicholson C., Rice M.E., Bohmaker K., Meller E. Extracellular dopamine concentration in the retina of the clawed frog, Xenopus laevis. Proc. Natl. Acad. Sci. USA. 90:1993;5667-5671.
56. Wulle I., Wagner H.-J. GABA and tyrosine hydroxylase immunocytochemistry reveal different patterns of colocalization in retinal neurons of various vertebrates. J. Comp. Neurol. 296:1990;173-178.
57. Zhou Z., Misler S. Amperometric detection of stimulus-induced quantal release of catecholamines from cultured superior cervical ganglion neurons. Proc. Natl. Acad. Sci. USA. 92:1995;6938-6942.
58. Zilberter Y., Kaiser K.M.M., Sakmann B. Dendritic GABA release depresses excitatory transmission between layer 2/3 pyramidal and bitufted neurons in rat neocortex. Neuron. 24:1999;979-988.