Direct visualization of the dendritic and receptive fields of directionally selective retinal ganglion cells.

Optical methods were used to locate the cell bodies of directionally selective ganglion cells in isolated rabbit retinas. These neurons detect the direction in which images move across the retinal surface and transmit that information to the brain. The receptive field of each identified cell was determined, after which the cell was injected with Lucifer yellow. An image of the receptive field border was then projected onto the fluorescent image of the dendrites, allowing precise comparison between them. The size of the receptive field matched closely the size of the dendritic arbor of that cell. This result restricts the types of convergence that can be postulated in modeling the mechanism of retinal directional selectivity.

[1]  F. Amthor,et al.  Morphology of on-off direction-selective ganglion cells in the rabbit retina , 1984, Brain Research.

[2]  T. Poggio,et al.  A synaptic mechanism possibly underlying directional selectivity to motion , 1978, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[3]  H. Wässle,et al.  Cholinergic amacrine cells of the rabbit retina contain glutamate decarboxylase and gamma-aminobutyrate immunoreactivity. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[4]  R H Masland,et al.  Autoradiographic identification of acetylcholine in the rabbit retina , 1979, The Journal of cell biology.

[5]  D. I. Vaney,et al.  ‘Coronate’ amacrine cells in the rabbit retina have the ‘starburst’ dendritic morphology , 1984, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[6]  R H Masland,et al.  Responses to acetylcholine of ganglion cells in an isolated mammalian retina. , 1976, Journal of neurophysiology.

[7]  H. Young,et al.  GABA-like immunoreactivity in cholinergic amacrine cells of the rabbit retina , 1988, Brain Research.

[8]  C. Brandon Cholinergic neurons in the rabbit retina: immunocytochemical localization, and relationship to GABAergic and cholinesterase-containing neurons , 1987, Brain Research.

[9]  S. Bloomfield Two types of orientation-sensitive responses of amacrine cells in the mammalian retina , 1991, Nature.

[10]  R H Masland,et al.  The shape and arrangement of the cholinergic neurons in the rabbit retina , 1984, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[11]  R. Masland,et al.  Co-release of acetylcholine and gamma-aminobutyric acid by a retinal neuron. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[12]  E. V. Famiglietti,et al.  Synaptic organization of starburst amacrine cells in rabbit retina: Analysis of serial thin sections by electron microscopy and graphic reconstruction , 1991, The Journal of comparative neurology.

[13]  E. V. Famiglietti,et al.  ‘Starburst’ amacrine cells and cholinergic neurons: mirror-symmetric ON and OFF amacrine cells of rabbit retina , 1983, Brain Research.

[14]  A. Ames,et al.  In Vitro Retina as an Experimental Model of the Central Nervous System , 1981, Journal of neurochemistry.

[15]  R. Masland,et al.  The functions of acetylcholine in the rabbit retina , 1984, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[16]  S. Bloomfield,et al.  Relationship between receptive and dendritic field size of amacrine cells in the rabbit retina. , 1992, Journal of neurophysiology.

[17]  T. Poggio,et al.  Retinal ganglion cells: a functional interpretation of dendritic morphology. , 1982, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[18]  F. Amthor,et al.  Morphologies of rabbit retinal ganglion cells with complex receptive fields , 1989, The Journal of comparative neurology.

[19]  N. Daw,et al.  Directionally sensitive ganglion cells in the rabbit retina: specificity for stimulus direction, size, and speed. , 1975, Journal of neurophysiology.