Hostname: page-component-848d4c4894-8bljj Total loading time: 0 Render date: 2024-07-04T23:56:32.406Z Has data issue: false hasContentIssue false

Synaptic inputs to retrogradely labeled ganglion cells in the retina of the cane toad, Bufo marinus

Published online by Cambridge University Press:  02 June 2009

Bao-Song Zhu
Affiliation:
Department of Anatomy and Histology and Center for Neuroscience, School of Medicine, The Flinders University of South Australia, Adelaide, Australia
Ian L. Gibbins
Affiliation:
Department of Anatomy and Histology and Center for Neuroscience, School of Medicine, The Flinders University of South Australia, Adelaide, Australia

Abstract

The entire population of ganglion cells in the retina of the toad Bufo marinus was labeled by retrograde transport of a lysine-fixable biotinylated dextran amine of 3000 molecular weight. Synaptic connections between bipolar, amacrine, and ganglion cells in the inner plexiform layer were quantitatively analyzed, with emphasis on synaptic inputs to labeled ganglion cell dendrites. Synapses onto ganglion cell dendrites comprised 47% of a total of 1234 identified synapses in the inner plexiform layer. Approximately half of the bipolar or amacrine cell synapses were directed onto ganglion cell dendrites, while the rest were made mainly onto amacrine cell dendrites. Most of the synaptic inputs to ganglion cell dendrites derived from amacrine cell dendrites (84%), with the rest from bipolar cell terminals. Synaptic inputs to ganglion cell dendrites were distributed relatively uniformly throughout all sublaminae of the inner plexiform layer. The present study provides unambiguous identification of ganglion cell dendrites including very fine processes, enabling a detailed analysis of the types and distribution of synaptic inputs from the bipolar and amacrine cell to the ganglion cells. The retrograde tracing technique used in the present study will prove to be a useful tool for identifying synaptic inputs to ganglion cell dendrites from neurochemically identified bipolar and amacrine cell types in the retina.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 1997

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bloomfield, S.A. & Miller, R.F. (1986). A functional organization of ON and OFF pathways in the rabbit retina. Journal of Neuroscience 6, 113.CrossRefGoogle Scholar
Buzás, P., Jeges, S. & Gábriel, R. (1996). The number and distribution of bipolar to ganglion cell synapses in the inner plexiform layer of the anuran retina. Visual Neuroscience 13, 10991107.CrossRefGoogle ScholarPubMed
Chng, S.-K. & Straznicky, C. (1992). The generation and changing retinal distribution of displaced amacrine cells in Bufo marinus from metamorphosis to adult. Anatomy and Embryology 186, 175181.Google Scholar
Dowling, J.E. (1968). Synaptic organization of the frog retina: An electron microscopic analysis comparing the retinas of frogs and primates. Proceedings of Royal Society B (London) 170, 205228.Google ScholarPubMed
Dubin, M.W. (1970). The inner plexiform layer of the vertebrate retina: A quantitative and comparative electron microscopic analysis. Journal of Comparative Neurology 140, 479506.Google Scholar
Famiglietti, E.V. (1992). Dendritic co-stratification of ON and ON-OFF directionally selective ganglion cells with starburst amacrine cells in rabbit retina. Journal of Comparative Neurology 324, 322335.CrossRefGoogle Scholar
Fritzsch, B. (1993). Fast axonal diffusion of 3000 molecular weight dextran amines. Journal of Neuroscience Methods 50, 95103.CrossRefGoogle ScholarPubMed
Gábriel, R. & Wilhelm, M. (1994). Quantitative synaptology of the inner plexiform layer of the retina of Bufo marinus. European Journal of Morphology 32, 1933.Google ScholarPubMed
Gábriel, R., Zhu, B.-S. & Straznicky, C. (1992). Synaptic contacts of tyrosine hydroxylase-immunoreactive elements in the inner plexiform layer of the retina of Bufo marinus. Cell Tissue Research 267, 525534.CrossRefGoogle ScholarPubMed
Gabriel, R., Zhu, B.-S. & Straznicky, C. (1993). Synaptic contacts of serotonin-like immunoreactive and 5,7-dihydroxytryptamine-accumulating neurons in the anuran retina. Neuroscience 54, 11031114.Google Scholar
Guiloff, G.D. & Kolb, H. (1994). Ultrastructural and immunocytochemical analysis of the circuitry of two putative directionally selective ganglion cells in turtle retina. Journal of Comparative Neurology 347, 321339.CrossRefGoogle ScholarPubMed
Guiloff, G.D., Jones, J. & Kolb, H. (1988). Organization of the inner plexiform layer of the turtle retina: An electron microscopic study. Journal of Comparative Neurology 272, 280292.CrossRefGoogle ScholarPubMed
Holmgren-Taylor, I. (1983). Synapses of the inner plexiform layer in the retina of cyprinid fish. Cell Tissue Research 229, 337350.Google ScholarPubMed
Kolb, H. & Famiglietti, E.V. (1974). Rod and cone pathways in the inner plexiform layer of cat retina. Science 186, 4749.Google Scholar
Kolb, H. & Nelson, R. (1993). OFF-alpha and OFF-beta ganglion cells in cat retina: II. Neural circuitry as revealed by electron microscopy of horseradish peroxidase stains. Journal of Comparative Neurology 329, 85110.Google Scholar
Koontz, M.A, & Hendrickson, A.E. (1987). Stratified distribution of synapses in the inner plexiform layer of primate retina. Journal of Comparative Neurology 263, 581592.CrossRefGoogle ScholarPubMed
Marshak, D., Ariel, M. & Brown, E. (1988). Distribution of synaptic inputs onto goldfish retinal ganglion cell dendrites. Experimental Eye Research 46, 965978.CrossRefGoogle ScholarPubMed
Muller, J.F., Ammermuller, J., Normann, R.A. & Kolb, H. (1991). Synaptic inputs to physiologically defined turtle retinal ganglion cells. Visual Neuroscience 7, 409429.CrossRefGoogle ScholarPubMed
Nguyen, V.S. & Straznicky, C. (1989). The development and the topographic organization of the retinal ganglion cell layer in Bufo marinus. Experimental Brain Research 75, 345353.Google Scholar
Weber, A.J. & Stanford, L.R. (1994). Synaptology of physiologically identified ganglion cells in the cat retina: A comparison of retinal X-and Y-cells. Journal of Comparative Neurology 343, 483499.CrossRefGoogle ScholarPubMed
Zhu, B.-S. & Gibbins, I. (1995). Synaptic circuitry of neuropeptide-containing amacrine cells in the retina of the cane toad, Bufo marinus. Visual Neuroscience 12, 919927.CrossRefGoogle ScholarPubMed
Zhu, B.-S., Straznicky, C. & Gibbins, I. (1995). Synaptic circuitry of serotonin-synthesizing and serotonin-accumulating amacrine cells in the retina of the cane toad, Bufo marinus. Visual Neuroscience 12, 1119.Google Scholar