Parallel processing in the mammalian retina: The proctor lecture

Investigative Ophthalmology and Visual Science

Volumn 40, Issue 7, 1999, Pages 1313-1327

  Boycott, Brian ^a   Wässle, Heinz ^b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b MAX PLANCK INSTITUTE FOR BRAIN RESEARCH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CONFERENCE PAPER; INFORMATION PROCESSING; NERVE PROJECTION; NONHUMAN; PRIORITY JOURNAL; RAT; RETINA; RETINA BIPOLAR GANGLION CELL; VISUAL INFORMATION;

ANIMALS; HUMANS; INTERNEURONS; OCULAR PHYSIOLOGY; PHOTOTRANSDUCTION; RECEPTORS, GLUTAMATE; RETINA; VISUAL PATHWAYS;

EID: 0033015229     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (143)

1. Stone J. Parallel Processing in the Visual System: The Classification of Retinal Ganglion Cells and Its Impact on the Neurobiology of Vision. New York: Plenum Press; 1983.
2. Rodieck RW, Brening RK, Watanabe M. The origin of parallel visual pathways. In: Shapley R, Lam DM-K, eds. Proceedings of the Retinal Research Foundation Symposia, Vol. 5, Contrast Sensitivity: From Receptors to Clinic. Cambridge, MA: MIT Press; 1993:117-144.
3. Kaplan E, Lee BB, Shapley RN. New views of primate retinal function. In: Osborne NN, Chader G, eds. Progress in Retinal Research. Oxford: Pergamon Press; 1990:273-336.
4. Lee BB. Receptive field structure in the primate retina. Vision Res. 1996;36:631-644.
5. Casagrande VA. A third parallel visual pathway to primate area VI. Trends Neurosci. 1994;17:305-310.
6. Hendry SHC, Yoshioka T. A neurochemically distinct third channel in the macaque dorsal lateral geniculate nucleus. Science. 1994;264:575-577.
7. Martin PR, White AJR, Goodchild AK, et al. Evidence that blue-on cells are part of the third geniculocortical pathway in primates. Eur J Neurosci. 1997;9:1536-1541.
8. Martin PR. Colour processing in the primate retina: recent progress. J Physiol. 1998;513:631-638.
9. Rodieck RW, Watanabe M. Survey of the morphology of macaque retinal ganglion cells that project to the pretectum, superior colliculus, and parvicellular laminae of the lateral geniculate nucleus. J Comp Neurol. 1993;338:289-303.
10. Pu M, Berson DM, Pan T. Structure and function of retinal ganglion cells innervating the cat's geniculate wing: an in vitro study. J Neurosci. 1994;14:4338-4358.
11. Stein JJ, Berson DM. On the distribution of gamma cells in the cat retina. Vis Neurosci. 1995;12:687-700.
12. Berson DM, Isayama T, Pu M. The eta ganglion cell type of cat retina. J Comp Neurol (in press).
13. Nelson R, Famiglietti EV Jr, Kolb H. Intracellular staining reveals different levels of stratification for on-and off-center ganglion cells in cat retina. J Neurophysiol. 1978;41:472-483.
14. Peichl L, Wässle H. Morphological identification of on- and off-centre brisk transient (Y) cells in the cat retina. Proc R Soc Lond B. 1981;212:139-156.
15. Jacoby R, Stafford D, Kouyama N, et al. Synaptic inputs to ON parasol ganglion cells in the primate retina. J Neurosci. 1996;16: 8041-8056.
16. Watanabe M, Rodieck RW. Parasol and midget ganglion cells of the primate retina. J Comp Neurol. 1989;289:434-454.
17. Dacey DM. Physiology, morphology and spatial densities of identified ganglion cell types in primate retina. In: Higher-Order Processing in the Visual System, Ciba Foundation Symposium 184. Chichester: Wiley; 1994:12-34.
18. Sterling P, Smith RG, Rao R, et al. Functional architecture of mammalian outer retina and bipolar cells. In: Djamgoz MBA, Archer SN, Vallerga S, eds. Neurobiology and Clinical Aspects of the Outer Retina. London: Chapman & Hall; 1995:323-348.
19. Jacobs GH. The distribution and nature of colour vision among the mammals. Biol Rev. 1993;68:413-471.
20. Moore RY, Speh JC, Card JP. The retinohypothalamic tract originates from a distinct subset of retinal ganglion cells. J Comp Neurol. 1995;352:351-366.
21. Boycott BB, Kolb H. The connections between bipolar cells and photoreceptors in the retina of the domestic cat. J Comp Neurol. 1973;148:91-114.
22. Dacheux RF, Raviola E. The rod pathway in the rabbit retina: a depolarizing bipolar and amacrine cell. J Neurosci. 1986;6:331-345.
23. Greferath U, Grünert U, Wässle H. Rod bipolar cells in the mammalian retina show protein kinase C-like immunoreactivity. J Comp Neurol. 1990;301:433-442.
24. Kolb H, Famiglietti EV. Rod and cone pathways in the inner plexiform layer of cat retina. Science. 1974;186:47-49.
25. Wässle H, Yamashita M, Greferath U, et al. The rod bipolar cell of the mammalian retina. Vis Neurosci. 1991;7:99-112.
26. Wässle H, Grünert U, Chun M-H, et al. The rod pathway of the macaque monkey retina: identification of All-amacrine cells with antibodies against calretinin. J Comp Neurol. 1995;361:537-551.
27. Cajal, SR y. La rétine des vertébrés. La Cellule. 1893;9:119-257.
28. Famiglietti EV. Functional architecture of cone bipolar cells in mammalian retina. Vision Res. 1981;21:1559-1563.
29. Mills SL, Massey SC. Morphology of bipolar cells labeled by DAPI in the rabbit retina. J Comp Neurol. 1992;321:133-149.
30. Merighi A, Raviola E, Dacheux RF. Connections of two types of flat cone bipolars in the rabbit retina. J Comp Neurol. 1996;371: 164-178.
31. Kolb H, Nelson R, Mariani A. Amacrine cells, bipolar cells and ganglion cells of the cat retina: a Golgi study. Vision Res. 1981; 21:1081-1114.
32. McGuire BA, Stevens JK, Sterling P. Microcircuitry of bipolar cells in the cat retina. J Neurosci. 1984;4:2920-2938.
33. Cohen ED, Sterling P. Demonstration of cell types among cone bipolar neurons of cat retina. Phil Trans R Soc Lond B. 1990; 330:305-321.
34. Cohen ED, Sterling P. Convergence and divergence of cones onto bipolar cells in the central area of the cat retina. Phil Trans R Soc Lond B. 1990;330:323-328.
35. Euler T, Wässle H. Immunocytochemical identification of cone bipolar cells in the rat retina. J Comp Neurol. 1995;361:461-478.
36. Szél A, Röhlich P, van Veen T. Short-wave sensitive cones in the rodent retina. Exp Eye Res. 1993;57:503-505.
37. Boycott BB, Wässle H. Morphological classification of bipolar cells in the macaque monkey retina. Eur J Neurosci. 1991;3: 1069-1088.
38. Polyak SL. The Retina. Chicago, IL: Chicago University Press; 1941.
39. Boycott BB, Dowling JE. Organization of the primate retina: light microscopy. Philos Trans R Soc Lond B Biol Sci. 1969;255:109-194.
40. Rauen T, Kanner BI. Localization of the glutamate transporter GLT-1 in rat and macaque monkey retinae. Neurosci Lett. 1994; 169:137-140.
41. Grünert U, Martin PR, Wässle H. Immunocytochemical analysis of bipolar cells in the macaque monkey retina. J Comp Neurol. 1994;348:607-627.
42. Milam AH, Dacey DM, Dizhoor AM. Recoverin immunoreactivity in mammalian cone bipolar cells. Vis Neurosci. 1993;10:1-12.
43. Wässle H, Grünert U, Martin PR, et al. Immunocytochemical characterization and spatial distribution of midget bipolar cells in the macaque monkey retina. Vision Res. 1994;34:562-579.
44. Kouyama N, Marshak DW. Bipolar cells specific for blue cones in the macaque retina. J Neurosci. 1992;12:1233-1252.
45. Cohen AJ. Some electron microscopic observations on interreceptor contacts in the human and macaque retinae. J Anat. 1965;99:595.
46. Baylor DA, Fuortes MGF, O'Bryan PM. Receptive fields of single cones in the retina of the turtle. J Physiol. 1971;214:265-294.
47. Raviola E, Gilula NV. Gap junctions between photoreceptor cells in the vertebrate retina. Proc Natl Acad Sci USA. 1973;70:1677-1681.
48. Tsukamoto Y, Masarachia P, Schein SJ, et al. Gap junctions between the pedicles of macaque foveal cones. Vision Res. 1992; 32:1809-1815.
49. Missotten L. The Ultrastructure of the Human Retina. Brussels: Arscia Uitgaven; 1965.
50. Dowling JE, Boycott BB. Organization of the primate retina: electron microscopy. Proc R Soc Lond B Biol Sci. 1966;166:80-111.
51. Chun M-H, Grünert U, Martin PR, et al. The synaptic complex of cones in the fovea and in the periphery of the macaque monkey retina. Vision Res. 1996;36:3383-3395.
52. Kolb H. Organization of the outer plexiform layer of the primate retina: electron microscopy of Golgi-impregnated cells. Phil Trans R Soc Lond B. 1970;258:261-283.
53. Raviola E, Gilula NV. Intramembrane organization of specialized contacts in the outer plexiform layer of the retina. J Cell Biol. 1975;65:192-222.
54. Boycott BB, Hopkins JM. Cone bipolar cells and cone synapses in the primate retina. Vis Neurosci. 1991;7:49-60.
55. Boycott BB, Hopkins JM. Cone synapses of a flat diffuse cone bipolar cell in the primate retina. J Neurocytol. 1993;22:765-778.
56. Kolb H, Boycott BB, Dowling JE. A second type of midget bipolar cell in the primate retina. Appendix. Phil Trans R Soc London B. 1969;255:177-184.
57. Hopkins JM, Boycott BB. The cone synapses of cone bipolar cells of primate retina. J Neurocytol. 1997;26:313-325.
58. Stell WK, Ishida AT, Lightfoot DO. Structural basis for on-and off-center responses in retinal bipolar cells. Science. 1977;198: 1269-1271.
59. Famiglietti EV Jr, Kaneko A, Tachibana M. Neuronal architecture of on and off pathways to ganglion cells in carp retina. Science. 1977;198:1267-1269.
60. Kolb H, Nelson R. The organization of photoreceptor to bipolar synapses in the outer plexiform layer. In: Djamgoz MBA, Archer SN, Vallerga S, eds. The Outer Retina. London: Chapman & Hall; 1995:273-296.
61. Hopkins JM, Boycott BB. Synaptic contacts of a two-cone flat bipolar cell in a primate retina. Vis. Neurosci. 1992;8:379-384.
62. Hopkins JM, Boycott BB. Synapses between cones and diffuse bipolar cells of a primate retina. J Neurocytol. 1995;24:680-694.
63. Hopkins JM, Boycott BB. The cone synapses of DB1 diffuse, DB6 diffuse and invaginating midget bipolar cells of a primate retina. J Neurocytol. 1996;25:391-403.
64. Vardi N, Morigiwa K, Wang T-L, et al. Neurochemistry of the mammalian cone 'synaptic complex.' Vision Res. 1998;38:1359-1369.
65. Calkins DJ, Tsukamoto Y, Sterling P. Foveal cones form basal as well as invaginating junctions with ON-diffuse bipolar cells. Vision Res. 1996;36:3373-3381.
66. Wässle H. Parallel pathways from the outer to the inner retina in primates. In: Gegenfurtner KR, Sharpe LT, eds. Colour Vision: From Genes to Perception. Cambridge, UK: Cambridge University Press; (in press).
67. Nelson R, Kolb H, Famiglietti EV Jr, et al. Neural responses in the rod and cone systems of the cat retina: intracellular records and procion stains. Invest Ophthalmol. 1976;15:946-953.
68. Nelson R, Kolb H. Synaptic patterns and response properties of bipolar and ganglion cells in the cat retina. Vision Res. 1983;23: 1183-1195.
69. Slaughter MM, Miller RF. 2-Amino-4-phosphonobutyric acid: a new pharmacological tool for retina research. Science. 1981;211: 182-185.
70. Shiells RA, Falk G, Naghshineh S. Action of glutamate and aspartate analogues on rod horizontal and bipolar cells. Nature. 1981; 294:592-594.
71. Attwell D, Mobbs P, Tessier-Lavigne M, et al. Neurotransmitter induced currents in retinal bipolar cells of the axolotl, Ambystoma mexicanum. J Physiol Lond. 1987;387:125-161.
72. Yamashita M, Wässle H. Responses of rod bipolar cells isolated from the rat retina to the glutamate agonist 2-amino-4-phosphonobutyric acid (APB). J Neurosci. 1991;11:2372-2382.
73. Villa de la P, Kurahashi T, Kaneko A. L-Glutamate-induced responses and cGMP-activated channels in three subtypes of retinal bipolar cells dissociated from the cat. J Neurosci. 1995;15:3571-3582.
74. Euler T, Schneider H, Wässle H. Glutamate responses of bipolar cells in a slice preparation of the rat retina. J Neurosci. 1996;16: 2934-2944.
75. Hartveit E. Membrane currents evoked by ionotropic glutamate receptor agonists in rod bipolar cells in the rat retinal slice preparation. J Neurophysiol. 1996;76:401-422.
76. Hartveit E. Functional organization of cone bipolar cells in the rat retina. J Neurophysiol. 1997;77:1716-1730.
77. DeVries SH, Schwartz EA. Kainate receptors mediate synaptic transmission between cones and "OFF" bipolar cells in a mammalian retina. Nature. 1999;397:157-160.
78. Cohen ED. Interactions of inhibition and excitation in the light-evoked currents of X type retinal ganglion cells. J Neurophysiol. 1998;80:2975-2990.
79. Euler T, Masland RH. Light responses recorded from bipolar cells in rat retinal slices. Soc Neurosci Abstr. 1998;24:S135. Abstract nr 57.6.
80. Hollmann M, Heinemann S. Cloned glutamate receptors. Annu Rev Neurosci. 1994;17:31-108.
81. Brandstätter JH, Koulen P, Wässle H. Diversity of glutamate receptors in the mammalian retina. Vision Res. 1998;38:1385-1397.
82. Lo W, Molloy R, Hughes TE. Ionotropic glutamate receptors in the retina: moving from molecules to circuits. Vision Res. 1998; 38:1399-1410.
83. Nomura A, Shigemoto R, Nakamura Y, et al. Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells. Cell. 1994;77:361-369.
84. Masu M, Iwakabe H, Tagawa Y, et al. Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene. Cell. 1995;80:757-765.
85. Koulen, P, Kuhn R, Wässle H, et al. Group I metabotropic glutamate receptors mGiuR1α and mGluR5a: localization in both synaptic layers of the rat retina. J Neurosci. 1997;17:2200-2211.
86. Hughes TE. Are there ionotropic glutamate receptors on the rod bipolar cell of the mouse retina? Vis Neurosci. 1997;14:103-109.
87. Wenzel A, Benke D, Möhler H, et al. N-methyl-D-aspartate receptors containing the NR2D subunit in the retina are selectively expressed in rod bipolar cells. Neuroscience. 1997;78:1105-1112.
88. Morigiwa K, Vardi N. Differential expression of ionotropic glutamate receptor subunits in the outer retina. J Comp Neurol. 1999;405:173-184.
89. Brandstätter JH, Koulen P, Wässle H. Selective synaptic distribution of kainate receptor subunits in the two plexiform layers of the rat retina. J Neurosci. 1997;17:9298-9307.
90. Qin P, Pourcho RG. Synaptic relationships of AMPA-selective glutamate receptor subunits in the cat retina. Vis Neurosci. 1999; 16:163-177.
91. Hartveit E, Brandstätter JH, Sassoè-Pognetto M, et al. Localization and developmental expression of the NMDA receptor subunit NR2A in the mammalian retina. J Comp Neurol. 1994;348:570-582.
92. Jeon C-J, Strettoi E, Masland RH. The major cell populations of the mouse retina. J Neurosci. 1998;18:8936-8946.
93. Peichl L, González-Soriano J. Morphological types of horizontal cell in rodent retinae: a comparison of rat, mouse, gerbil, and guinea pig. Vis Neurosci. 1994;11:501-517.
94. Kolb H, Mariani A, Gallego A. A second type of horizontal cell in the monkey retina. J Comp Neurol. 1980;189:31-44.
95. Boycott BB, Hopkins JM, Sperling HG. Cone connections of the horizontal cells of the rhesus monkey's retina. Proc R Soc Lond Biol. 1987;229:345-379.
96. Kolb H. Anatomical pathways for color vision in the human retina. Vis Neurosci. 1991;7:61-74.
97. Kolb H. The architecture of functional neural circuits in the vertebrate retina. Invest Ophthalmol Vis Sci. 1994;35:2385-2404.
98. Dacey DM, Lee BB. The 'blue-on' opponent pathway in primate retina originates from a distinct bistratified ganglion cell type. Nature. 1994;367:731-735.
99. Calkins DJ, Tsukamoto Y, Sterling P. Microcircuitry and mosaic of a blue-yellow ganglion cell in the primate retina. J Neurosci. 1998;18:3373-3385.
100. Ghosh KK, Martin PR, Grünert U. Morphological analysis of the blue cone pathway in the retina of a new world monkey, the Callithrix jacchus. J Comp Neurol. 1997:211-225.
101. Dacey DM. Morphology of a small-field bistratified ganglion cell type in the macaque and human retina. Vis Neurosci. 1993;10: 1081-1098.
102. Dacey DM. Circuitry for color coding in the primate retina. Proc Natl Acad Sci USA. 1996;93:582-588.
103. Calkins DJ. Synaptic organization of cone pathways in the primate retina. In: Gegenfurtner KR, Sharpe LT, eds. Colour Vision: From Genes to Perception. Cambridge, UK: Cambridge University Press; (in press).
104. Mollon JD, Bowmaker JK. The spatial arrangement of cones in the primate fovea. Nature. 1992;360:677-679.
105. Kolb H, DeKorver L. Midget ganglion cells of the parafovea of the human retina: a study by electron microscopy and serial-section reconstructions. J Comp Neurol. 1991;303:617-636.
106. Calkins DJ, Schein SJ, Tsukamoto Y, et al. M and L cones in macaque fovea connect to midget ganglion cells by different numbers of excitatory synapses. Nature. 1994;371:70-72.
107. Reid RC, Shapley RM. Spatial structure of cone inputs to receptive fields in primate lateral geniculate nucleus. Nature. 1992; 356:716-718.
108. Smith VC, Pokorny J, Lee BB, et al. Responses of ganglion cells of the macaque retina on changing the relative phase of heterochromatically modulated light. J Physiol. 1992;458:191-221.
109. Kremers J, Lee BB, Yeh T. Receptive field dimensions of primate retinal ganglion cells. In: Drum B, ed. Color Vision Deficiencies XII. Dordrecht: Kluwer Academic Publishers; 1995:399-406.
110. Wässle H, Boycott BB, Röhrenbeck J. Horizontal cells in the monkey retina: cone connections and dendritic network. Eur J Neurosci. 1989;1:421-435.
111. Dacheux RF, Raviola E. Physiology of H1 horizontal cells in the primate retina. Proc R Soc Lond B Biol Sci. 1990;239:213-230.
112. Dacey DM, Lee BB, Stafford DK, et al. Horizontal cells of the primate retina: cone specificity without spectral opponency. Science. 1996;271:656-659.
113. Calkins DJ, Sterling P. Absence of spectrally specific lateral inputs to midget ganglion cells in primate retina. Nature. 1996;381:613-615.
114. Paulus W, Kröger-Paulus A. A new concept of retinal colour coding. Vision Res. 1983;23:529-540.
115. Lennie P, Haake PW, Williams DR. The design of chromatically opponent receptive fields. In: Landy MS, Movshon JA, eds. Computational Models of Visual Processing. London: MIT Press; 1992:71-82.
116. Wässle H. Grünert U, Röhrenbeck J, et al. Retinal ganglion cell density and cortical magnification factor in the primate. Vision Res. 1990;30:1897-1911.
117. Dacey DM, Petersen MR. Dendritic field size and morphology of midget and parasol ganglion cells of the human retina. Proc Natl Acad Sci USA. 1992;89:9666-9670.
118. Dacey DM. The mosaic of midget ganglion cells in the human retina. J Neurosci. 1993b;13:5334-5355.
119. Croner LJ, Kaplan E. Receptive fields of P and M ganglion cells across the primate retina. Vision Res. 1995;35:7-24.
120. Roorda A, Williams DR. The arrangement of the three cone classes in the living human eye. Nature. 1999;397:520-522.
121. Mullen KT, Kingdom FAA. Losses in peripheral colour sensitivity predicted from "hit and miss" post-receptoral cone connections. Vision Res. 1996;36:1995-2000.
122. Scholes JH. Colour receptors, and their synaptic connexions, in the retina of a cyprinid fish. Philos Trans R Soc Lond B Biol Sci. 1975;270:61-118.
123. Ishida AT, Stell WK, Lightfoot DO. Rod and cone inputs to bipolar cells in goldfish retina. J Comp Neurol. 1980;191:315-335.
124. Nawy S, Copenhagen DR. Multiple classes of glutamate receptor on depolarizing bipolar cells in retina. Nature. 1987;325:56-58.
125. Nawy S, Copenhagen DR. Intracellular cesium separates two glutamate conductances in retinal bipolar cells of goldfish. Vision Res. 1990;30:967-972.
126. Calkins DJ, Schein SJ, Sterling P. Cone inputs to three types of non-midget ganglion cell in macaque fovea. [ARVO Abstract]. Invest Ophthalmol Vis Sci. 1995;36(4):S4. Abstract nr 15.
127. Jacoby RA, Marshak DW. Diffuse bipolar cell inputs to parasol ganglion cells in macaque retina. [ARVO Abstract]. Invest Ophthalmol Vis Sci. 1995;36(4):S4. Abstract nr 16.
128. Jacoby RA, Marshak DW. Inputs to parasol ganglion cells in macaque retina. [ARVO Abstract]. Invest Ophtalmol Vis Sci. 1996;37(3):S950. Abstract nr 4349.
129. Lee BB, Martin PR, Valberg A. Nonlinear summation of M-and L-cone inputs to phasic retinal ganglion cells of the macaque. J Neurosci. 1989;9.1433-1442.
130. Lee BB, Pokorny J, Smith VC. et al. Responses to pulses and sinusoids in macaque ganglion cells. Vision Res. 1994;34:3081-3096.
131. A receptors with the directionally selective circuitry of the rat retina. Vis Neurosci. 1995;12:345-358.
132. Wässle H, Boycott BB. Functional architecture of the mammalian retina. Physiol Rev. 1991;71:447-480.
133. Lee BB, Wehrhahn C, Westheimer G, et al. The spatial precision of macaque ganglion cell responses in relation to vernier acuity of human observers. Vision Res. 1995;35:2743-2758.
134. Mittman S, Taylor WR, Copenhagen DR. Concomitant activation of two types of glutamate receptor mediates excitation of salamander retinal ganglion cells. J Physiol. 1990;428:175-197.
135. Mollon JD, Jordan G. Eine evolutionäre Interpretation des menschlichen Farbensehens. Die Farbe. 1988;35/36:139-170.
136. Osorio D, Vorobyev M. Colour vision as an adaptation of frugivory in primates. Proc R Soc Lond B. 1996;263:593-599.
137. Regan BC, Viénot F, Charles-Dominique PC, et al. The colour signals that fruits present to primates. [ARVO Abstract]. Invest Ophthalmol Vis Sci. 1996;37(3):S648. Abstract nr 2997.
138. Shatz CJ. Emergence of order in visual system development. Proc Natl Acad Sci USA. 1996;93:602-608.
139. Ingling CR Jr, Martinez-Uriegas E. The relationship between spectral sensitivity and spatial sensitivity for the primate r-g X-channel. Vision Res. 1983;23:1495-1500.
140. Ingling CR Jr, Martinez-Uriegas E. The spatio-chromatic signal of the r-g channel. In: Mollon JD, Sharpe LT, eds. Colour Vision: Physiology and Psychophysics. London: Academic Press; 1983: 433-444.
141. Lennie P. Recent developments in the physiology of color vision. Trends Neurosci. 1984;7:243-248.
142. Merigan WH. Chromatic and achromatic vision of macaques: role of the P pathway. J Neurosci. 1989;9:776-783.
143. Negishi K, Kato S, Teranishi T. Dopamine cells and rod bipolar cells contain protein kinase C-like immunoreactivity in some vertebrate retinas. Neurosci Lett. 1988;94:247-252.