AMPA receptor is involved in transmission of cone signal to ON bipolar cells in carp retina

Brain Research

Volumn 1002, Issue 1-2, 2004, Pages 86-93

  Huang, Hai ^a,b   Luo, Dong Gen ^a,b   Shen, Yin ^a   Zhang, Ai Jun ^a   Yang, Ru ^b   Yang, Xiong Li ^a  

^a FUDAN UNIVERSITY   (China)

^b Shanghai Jiao Tong University Affiliated Sixth People s Hospital   (China)

Author keywords

AMPA receptor; Bipolar cell; Carp retina; ON signal pathway

Indexed keywords

1 (4 AMINOPHENYL) 4 METHYL 7,8 METHYLENEDIOXY 5H 2,3 BENZODIAZEPINE; ALPHA AMINO 3 HYDROXY 5 METHYL 4 ISOXAZOLEPROPIONIC ACID; AMPA RECEPTOR; AMPA RECEPTOR ANTAGONIST; COBALT; GLUTAMIC ACID; PICROTOXIN; STRYCHNINE;

ANIMAL CELL; ARTICLE; CARP; CONTROLLED STUDY; DEPOLARIZATION; HYPERPOLARIZATION; INTRACELLULAR RECORDING; MEMBRANE POTENTIAL; NEUROTRANSMISSION; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FUNCTION; RETINA AMACRINE CELL; RETINA BIPOLAR GANGLION CELL; RETINA CONE; SIGNAL TRANSDUCTION;

EID: 1342321764     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2003.12.019     Document Type: Article

References (45)

1. Attwell D., Mobbs P., Tessier-Lavigne M., Wilson M. Neurotransmitter induced currents in retinal bipolar cells of the axolotl, Ambystoma mexicanum. J. Physiol. (Lond.). 387:1987;125-161.
2. Chen Y.C., Kung S.S., Chen B.Y., Hung C.C., Chen C.C., Wang T.Y., Wu Y.M., Lin W.H., Tzeng C.S., Chow W.Y. Identifications, classification, and evolution of the vertebrate alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptor subunit genes. J. Mol. Evol. 53:2001;690-702.
3. Connaughton V.P., Nelson R. Axonal stratification patterns and glutamate-gated conductance mechanisms in zebrafish retinal bipolar cells. J. Physiol. (Lond.). 524:2000;125-146.
4. DeMarco P.J. Jr., Bilotta J., Powers M.K. DL-2-amino-4-phosphonobutyric acid does not eliminate "ON" responses in the visual system of goldfish. Proc. Natl. Acad. Sci. U. S. A. 88:1991;3787-3791.
5. DeVries S.H., Schwartz E.A. Kainate receptors mediate synaptic transmission between cones and 'off' bipolar cells in a mammalian retina. Nature. 379:1999;57-160.
6. Dowling J.E. The Retina: An Approachable Part of the Brain. 1987;Belknap Press of Harvard Univ. Press, Massachusetts.
7. Eliasof S., Werblin F. Characterization of the glutamate transporter in retinal cones of the tiger salamander. J. Neurosci. 13:1993;402-411.
8. Grant G.B., Dowling J.E. A glutamate-activated chloride current in cone-driven ON bipolar cells of the white perch retina. J. Neurosci. 15:1995;3852-3862.
9. Grant G.B., Dowling J.E. ON bipolar cell responses in the teleost retina are generated by two distinct mechanisms. J. Neurophysiol. 76:1996;3842-3849.
10. Hughes T.E. Are there ionotropic glutamate receptors on the rod bipolar cell of the mouse retina? Vis. Neurosci. 14:1997;103-109.
11. Hughes T.E., Hermans-Borgmeyer I., Heinemann S. Differential expression of glutamate receptor genes (GluR1-5) in the rat retina. Vis. Neurosci. 8:1992;49-55.
12. Kalloniatis M., Tomisich G. Amino acid neurochemistry of the vertebrate retina. Prog. Retin. Eye Res. 18:1999;811-866.
13. Kamphuis W., Klooster J., Dijk F. Expression of AMPA-type glutamate receptor subunit (GluR2) in ON-bipolar neurons in the rat retina. J. Comp. Neurol. 455:2003;172-186.
14. Kaneko A. Physiological and morphological identification of horizontal, bipolar and amacrine cells in goldfish retina. J. Physiol. (Lond.). 207:1970;623-633.
15. Kaneko A. Synaptic transmission from photoreceptors to bipolar and horizontal cells in the carp retina. Cold Spring Harbor Symp. Quant. Biol. 40:1976;537-546.
16. Kato S., Negishi K., Teranishi T., Ishita S. The use of the carp retina in neurobiology: its uniqueness and application for neural network analyses of the inner retina. Prog. Neurobiol. 37:1991;287-327.
17. Klooster J., Studholme K.M., Yazulla S. Localization of the AMPA subunit GluR2 in the outer plexiform layer of goldfish retina. J. Comp. Neurol. 441:2001;155-167.
18. A receptors. Brain Res. 958:2002;222-226.
19. Masu M., Iwakabe H., Togawa Y., Miyoshi T., Yamashita M., Fukuda Y., Sasaki H., Hiroi K., Nakamura Y., Shigemoto R., Takada M., Nakamura K., Nakao K., Katsuki M., Nakanishi S. Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene. Cell. 80:1995;757-765.
20. Miller R.F., Slaughter M.M. Excitatory amino acid in the vertebrate retina. Morgan W.W. Retinal Transmitters and Modulators: Models for the Brain. 1985;123-160 CRC press, Boca Raton.
21. Nawy S., Copenhagen D.R. Multiple classes of glutamate receptor on depolarizing bipolar cells in retina. Nature. 325:1987;56-58.
22. Nawy S., Copenhagen D.R. Intracellular cesium separates two glutamate conductances in retinal bipolar cells of goldfish. Vis. Res. 30:1990;967-972.
23. Palmer M.J., Taschenberger H., Hull C., Tremere L., von Gersdorff H. Synaptic activation of presynaptic glutamate transporter currents in nerve terminals. J. Neurosci. 23:2003;4831-4841.
24. Partin K.M., Patneau D.K., Winters C.A., Mayer M.L., Buonanno A. Selective modulation of desensitization at AMPA versus kainate receptors by cyclothiazide and concanavalin A. Neuron. 11:1993;1069-1082.
25. Paternain A.V., Morales M., Lerma J. Selective antagonism of AMPA receptors unmasks kainate receptor-mediated responses in hippocampal neurons. Neuron. 14:1995;185-189.
26. Peng Y.W., Blackstone C.D., Huganir R.L., Yau K.W. Distribution of glutamate receptor subtypes in the vertebrate retina. Neuroscience. 66:1995;483-497.
27. Saito T., Kujiraoka T. Physiological and morphological identification of two types of on-center bipolar cells in the carp retina. J. Neurophysiol. 205:1982;161-170.
28. Sarantis M., Everett K., Attwell D. A presynaptic action of glutamate at the cone output synapse. Nature. 332:1988;451-453.
29. Schiller P.H. The ON and OFF channels of the visual system. Trends Neurosci. 15:1992;86-92.
30. Schiller P.H., Sandell J.H., Maunsell J.H. Functions of the ON and OFF channels of the visual system. Nature. 322:1986;824-825.
31. Schultz K., Janssen-Bienhold U., Weiler R. Selective synaptic distribution of AMPA and kainate receptor subunits in the outer plexiform layer of the carp retina. J. Comp. Neurol. 435:2001;433-449.
32. Shen Y., Zhou Y., Yang X.L. Characterization of AMPA receptors on isolated amacrine-like cells in carp retina. Eur. J. Neurosci. 11:1999;4233-4240.
33. Slaughter M.M., Miller R.F. 2-Amino-4-phosphonobutyric acid: a new pharmacological tool for retina research. Science. 211:1981;182-184.
34. Tachibana M., Kaneko A. L-glutamate-induced depolarization in solitary photoreceptors: a process that may contribute to the interaction between photoreceptors in situ. Proc. Natl. Acad. Sci. U. S. A. 85:1988;5315-5319.
35. Thoreson W.B., Witkovsky P. Glutamate receptors and circuits in the vertebrate retina. Prog. Retin. Eye Res. 18:1999;765-810.
36. Tornqvist K., Yang X.L., Dowling J.E. Modulation of cone horizontal cell activity in the teleost fish retina: III. Effects of prolonged darkness and dopamine on electrical coupling between horizontal cells. J. Neurosci. 8:1988;2279-2288.
37. Vardi N., Morigiwa K., Wang T.L., Shi Y.J., Sterling P. Neurochemistry of the mammalian cone 'synaptic complex'. Vis. Res. 38:1998;1359-1369.
38. Wenzel A., Benke D., Mohler H., Fritschy J.M. N-methyl-D-aspartate receptors containing the NR2D subunit in the retina are selectively expressed in rod bipolar cells. Neuroscience. 78:1997;1105-1112.
39. Werblin F.S., Dowling J.E. Organization of the retina of the mudpuppy, Necturus maculosus: II. Intracellular recording. J. Neurophysiol. 32:1969;339-355.
40. Wu S.M., Maple B.R. Amino acid neurotransmitters in the retina: a functional overview. Vis. Res. 38:1998;1371-1384.
41. Wu S.M., Yang X.L. Functional characterization of amino acid neurotransmitters in the outer retina. Neurosci. Res. (Suppl. 15):1991;S117-S130.
42. 2+ on signal transmission from rods and cones to bipolar cells in carp retina. Brain Res. 957:2002;136-143.
43. Xu H.P., Luo D.G., Yang X.L. Signals from cone photoreceptors to L-type horizontal cells are differentially modulated by low calcium in carp retina. Eur. J. Neurosci. 13:2001;1411-1419.
44. Yang X.L., Wu S.M. Feedforward lateral inhibition in retinal bipolar cells: input-output relation of the horizontal cell-depolarizing bipolar cell synapse. Proc. Natl. Acad. Sci. U. S. A. 88:1991;3310-3313.
45. A receptors in carp retina. Brain Res. 759:1997;160-162.