Glycinergic synaptic transmission to bullfrog retinal bipolar cells is input-specific

Neuroscience

Volumn 113, Issue 4, 2002, Pages 779-784

  Du, J L ^a,b   Yang, X L ^a,b  

^a FUDAN UNIVERSITY   (China)

^b INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

Author keywords

Glycine receptor; Peak scaled non stationary noise analysis; Retinal slice preparation; Single channel conductance; Whole cell recording

Indexed keywords

GLYCINE; GLYCINE RECEPTOR;

ADOLESCENT; ANIMAL CELL; ARTICLE; CLAMP; CONTROLLED STUDY; DENDRITE; ELECTRIC CONDUCTIVITY; INHIBITION KINETICS; INHIBITORY POSTSYNAPTIC POTENTIAL; LABORATORY; NERVE ENDING; NONHUMAN; PRIORITY JOURNAL; RETINA AMACRINE CELL; RETINA BIPOLAR GANGLION CELL; RETINA INNER PLEXIFORM LAYER; SIGNAL NOISE RATIO; SIGNAL TRANSDUCTION; SYNAPTIC TRANSMISSION; TIME;

ANIMALS; DENDRITES; NEURAL INHIBITION; RANA CATESBEIANA; RECEPTORS, GLYCINE; RETINA; SYNAPTIC TRANSMISSION;

EID: 0037056014     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0306-4522(02)00255-5     Document Type: Article

References (43)

1. Auger C., Marty A. Heterogeneity of functional synaptic parameters among single release sites. Neuron. 19:1997;139-150.
2. A receptors suggest differential targeting of receptor subtypes. J. Neurosci. 19:1999;2960-2973.
3. Colquhoun D., Hawkes S.G. Relaxation and fluctuations of membrane currents that flow through drug-operated channels. Proc. R. Soc. London B. 199:1977;231-262.
4. Cook P.B., Lukasiewicz P.D., McReynolds J.S. Action potentials are required for the lateral transmission of glycinergic transient inhibition in the amphibian retina. J. Neurosci. 18:1998;2301-2308.
5. Craig A.M., Boudin H. Molecular heterogeneity of central synapses: afferent and target regulation. Nat. Neurosci. 4:2001;569-578.
6. A receptor channels. J. Neurophysiol. 71:1994;1318-1335.
7. Deng P., Cuenca N., Doerr T., Pow D.V., Miller R., Kolb H. Localization of neurotransmitter and calcium binding proteins to neurons of salamander and mudpuppy retinas. Vis. Res. 41:2001;1771-1783.
8. Dowling, J.E., 1987. The Retina: An Approachable Part of the Brain, Belknap Press of Harvard University Press, Cambridge, MA, pp. 108-116.
9. Du J.L., Yang X.L. Retinal bipolar cells: a model for studying neuronal signal integration. Chin. Sci. Bull. 44:1999;1437-1443.
10. C receptors on bullfrog retinal bipolar cells. J. Neurophysiol. 84:2000;666-676.
11. Enz R., Bormann J. Expression of glycine receptor subunits and gephyrin in single bipolar cells of the rat retina. Vis. Neurosci. 12:1995;501-507.
12. Fischer F., Kneussel M., Tintrup H., Haverkamp S., Rauen T., Betz H., Wässle H. Reduced synaptic clustering of GABA and glycine receptors in the retina of the gephrin null mutant mouse. J. Comp. Neurol. 427:2000;634-648.
13. Gardner S.M., Trussell L.O., Oertel D. Time course and permeation of synaptic AMPA receptors in cochlear nuclear neurons correlate with input. J. Neurosci. 19:1999;8721-8729.
14. Gardner S.M., Trussell L.O., Oertel D. Correlation of AMPA receptor subunit composition with synaptic input in the mammalian cochlear nuclei. J. Neurosci. 21:2001;7428-7437.
15. Greferath U., Brandstätter J.H., Wässle H., Kirsch J., Kuhse J., Grünert U. Differential expression of glycine receptor subunits in the retina of the rat: a study using immunohistochemistry and in situ hybridization. Vis. Neurosci. 11:1994;721-729.
16. Grünert U., Wässle H. Immunocytochemical localization of glycine receptors in the mammalian retina. J. Comp. Neurol. 335:1993;523-537.
17. Han Y., Zhang J., Slaughter M.M. Partition of transient and sustained inhibitory glycinergic inputs to retinal ganglion cells. J. Neurosci. 17:1997;3392-3440.
18. Hines M.L., Carnevale N.T. The NEURON simulation environment. Neural Comput. 9:1997;1179-1209.
19. Landsend A.S., Amiry-Moghaddam M., Matsubara A., Bergersen L., Usami S., Wenthold R.J., Ottersen O.P. Differential localization of delta glutamate receptors in the rat cerebellum: coexpression with AMPA receptors in parallel fiber-spine synapses and absence from climbing fiber-spine synapses. J. Neurosci. 17:1997;834-842.
20. Maple B.R., Wu S.M. Glycinergic synaptic inputs to bipolar cells in the salamander retina. J. Physiol. 506:1998;731-744.
21. Marc, R.E., 1985. The role of glycine in retinal circuitry. In: Morgan, W.H. (Ed.), Retinal Transmitters and Modulators: Models for the Brain, vol. 1. CRC, Boca Raton, FL, pp. 119-158.
22. Nusser Z. AMPA and NMDA receptors: similarities and differences in their synaptic distribution. Curr. Opin. Neurobiol. 10:2000;337-341.
23. A receptor number underlie variation in GABA mini amplitude. Neuron. 19:1997;697-709.
24. Nusser Z., Naylor D., Mody I. Synapse-specific contribution of the variance of transmitter concentration to the decay of inhibitory postsynaptic currents. Biophys. J. 80:2001;1251-1261.
25. Nusser Z., Sieghart W., Benke D., Frischy J.M., Somogyi P. Differential synaptic localization of two major γ-aminobutyric acid type A receptor α subunits on hippocampal pyramidal cells. Proc. Natl. Acad. Sci. USA. 93:1996;11939-11944.
26. A receptors in rat hippocampus. Neuron. 10:1993;189-200.
27. Rall W. Time constants and electrotonic length of membrane cylinders and neurons. Biophys. J. 9:1969;1483-1508.
28. Robinson H.P.C., Sahara Y., Kawai N. Nonstationary fluctuation analysis and direct resolution of single-channel currents at postsynaptic sites. Biophys. J. 59:1991;295-304.
29. Rubio M.E., Wenthold R.J. Glutamate receptors are selectively targeted to postsynaptic sites in neurons. Neuron. 18:1997;939-950.
30. Sassoè-Pognetto M., Wässle H., Grunert U. Glycinergic synapses in the rod pathway of the rat retina: cone bipolar cells express the α1 subunit of the glycine receptor. J. Neurosci. 14:1994;5113-5146.
31. Sigworth F.J. The variance of sodium current fluctuations at the node of Ranvier. J. Physiol. 307:1980;97-129.
32. Singer J.H., Berger A.J. Contribution of single-channel properties to the time course and amplitude variance of quantal glycine currents recorded in rat motoneurons. J. Neurophysiol. 81:1999;1608-1616.
33. Smiley J.F., Basinger S.F. Somatostatin-like immunoreactivity and glycine high-affinity uptake colocalize to an interplexiform cell of the Xenopus laevis retina. J. Comp. Neurol. 274:1988;608-618.
34. Smiley J.F., Yazulla S. Glycinergic contacts in the outer plexiform layer of the Xenopus laevis retina characterized by antibodies to glycine, GABA, and glycine receptors. J. Comp. Neurol. 299:1990;375-388.
35. Spruston N., Jaffe D.B., Williams S.H., Johnston D. Voltage- and space-clamp errors associated with the measurement of electrotonically remote synaptic events. J. Neurophysiol. 70:1993;781-802.
36. Stone S., Schütte M. Physiological and morphological properties of OFF- and ON-center bipolar cells in the Xenopus retina: effects of glycine and GABA. Vis. Neurosci. 7:1991;363-376.
37. Tóth K., McBain C.J. Afferent-specific innervation of two distinct AMPA receptor subtypes on single hippocampal interneurons. Nat. Neurosci. 1:1998;572-578.
38. Tóth K., McBain C.J. Target-specific expression of pre- and postsynaptic mechanisms. J. Physiol. 525:2000;41-51.
39. Traynelis S.F., Jaramillo F. Getting the most out of noise in the central nervous system. Trends Neurosci. 21:1998;137-145.
40. Traynelis S.F., Silver R.A., Cull-Candy S.G. Estimated conductance of glutamate receptor channels activated during EPSCs at the cerebellar mossy fiber-granule cell synapse. Neuron. 11:1993;279-289.
41. Wang Y.X., Wenthold R.J., Ottersen O.P., Petralia R.S. Endbulb synapses in the anteroventral cochlear nucleus express a specific subset of AMPA-type glutamate receptor subunits. J. Neurosci. 18:1998;1148-1160.
42. Wässle H., Koulen P., Brandstätter J.H., Fletcher E.L., Becker C.M. Glycine and GABA receptors in the mammalian retina. Vis. Res. 38:1998;1411-1430.
43. Wu S.M., Maple B.R. Amino acid neurotransmitters in the retina: a functional overview. Vis. Res. 38:1998;1371-1384.