Spatial scale and cellular substrate of contrast adaptation by retinal ganglion cells (original) (raw)
Shapley, R. & Enroth-Cugell, C. Visual adaptation and retinal gain controls. Prog. Ret. Res.3, 263–346 (1984). Article Google Scholar
Shapley, R. & Victor, J. D. The effect of contrast on the transfer properties of cat retinal ganglion cells. J. Physiol. Lond.285, 275–298 (1978). ArticleCAS Google Scholar
Shapley, R. M. & Victor, J. D. Nonlinear spatial summation and the contrast gain control of cat retinal ganglion cells. J. Physiol. Lond.290, 141–161 (1979). ArticleCAS Google Scholar
Shapley, R. M. & Victor, J. D. The effect of contrast on the non-linear response of the Y cell. J. Physiol. Lond.302, 535–547 (1980). ArticleCAS Google Scholar
Shapley, R. M. & Victor, J. D. How the contrast gain control modifies the frequency responses of cat retinal ganglion cells. J. Physiol. Lond.318, 161–179 (1981). ArticleCAS Google Scholar
Benardete, E. A., Kaplan, E. & Knight, B. W. Contrast gain control in the primate retina: P cells are not X-like, some M cells are. Vis. Neurosci.8, 483–486 (1992). ArticleCAS Google Scholar
Enroth-Cugell, C. & Jakiela, H. G. Suppression of cat retinal ganglion cell responses by moving patterns. J. Physiol. Lond.302, 49–72 (1980). ArticleCAS Google Scholar
Smirnakis, S. M., Berry, M. J., Warland, D. K., Bialek, W. & Meister, M. Adaptation of retinal processing to image contrast and spatial scale. Nature386, 69–73 (1997). ArticleCAS Google Scholar
Shapley, R. Retinal physiology: adapting to the changing scene. Curr. Biol.7, R421–423 (1997). ArticleCAS Google Scholar
Albrecht, D. G., Farrar, S. B. & Hamilton, D. B. Spatial contrast adaptation characteristics of neurones recorded in the cat's visual cortex. J. Physiol. Lond.347, 713–739 (1984). ArticleCAS Google Scholar
Ohzawa, I., Sclar, G. & Freeman, R. D. Contrast gain control in the cat's visual system. J. Neurophysiol.54, 651–667 (1985). ArticleCAS Google Scholar
Sanchez-Vives, M. V., Nowak, L. G. & McCormick, D. A. Membrane mechanisms underlying contrast adaptation in cat area 17 in vivo. J. Neurosci.20, 4267–4285 (2000). ArticleCAS Google Scholar
Maddess, T., McCourt, M. E., Blakeslee, B. & Cunningham, R. B. Factors governing the adaptation of cells in area-17 of the cat visual cortex. Biol. Cybern.59, 229–236 (1988). ArticleCAS Google Scholar
Vaney, D. I. The mosaic of amacrine cells in the mammalian retina. Prog. Ret. Res.9, 49–100 (1991). Article Google Scholar
MacNeil, M. A. & Masland, R. H. Extreme diversity among amacrine cells: implications for function. Neuron20, 971–982 (1998). ArticleCAS Google Scholar
MacNeil, M. A., Heussy, J. K., Dacheux, R. F., Raviola, E. & Masland, R. H. The shapes and numbers of amacrine cells: matching of photofilled with Golgi-stained cells in the rabbit retina and comparison with other mammalian species. J. Comp. Neurol.413, 305–326 (1999). ArticleCAS Google Scholar
Koontz, M. A., Hendrickson, L. E., Brace, S. T. & Hendrickson, A. E. Immunocytochemical localization of GABA and glycine in amacrine and displaced amacrine cells of macaque monkey retina. Vision Res.33, 2617–2628 (1993). ArticleCAS Google Scholar
Kalloniatis, M., Marc, R. E. & Murry, R. F. Amino acid signatures in the primate retina. J. Neurosci.16, 6807–6829 (1996). ArticleCAS Google Scholar
Crook, D. K. & Pow, D. V. Analysis of the distribution of glycine and GABA in amacrine cells of the developing rabbit retina: a comparison with the ontogeny of a functional GABA transport system in retinal neurons. Vis. Neurosci.14, 751–763 (1997). ArticleCAS Google Scholar
Ehinger, B., Ottersen, O. P., Storm-Mathisen, J. & Dowling, J. E. Bipolar cells in the turtle retina are strongly immunoreactive for glutamate. Proc. Natl. Acad. Sci. USA85, 8321–8325 (1988). ArticleCAS Google Scholar
Lukasiewicz, P. D. & Wong, R. O. L. GABAC receptors on ferret retinal bipolar cells: A diversity of subtypes in mammals? Vis. Neurosci.14, 989–994 (1997). ArticleCAS Google Scholar
Mills, S. L. & Massey, S. C. Distribution and coverage of A- and B-type horizontal cells stained with Neurobiotin in the rabbit retina. Vis. Neurosci.11, 549–560 (1994). ArticleCAS Google Scholar
Peters, B. N. & Masland, R. H. Responses to light of starburst amacrine cells. J. Neurophysiol.75, 469–480 (1996). ArticleCAS Google Scholar
Taylor, W. R. & Wässle, H. Receptive field properties of starburst cholinergic amacrine cells in the rabbit retina. Eur. J. Neurosci.7, 2308–2321 (1995). ArticleCAS Google Scholar
Stafford, D. K. & Dacey, D. M. Physiology of the A1 amacrine: a spiking, axon-bearing interneuron of the macaque monkey retina. Vis. Neurosci.14, 507–522 (1997). ArticleCAS Google Scholar
Taylor, W. R. Response properties of long-range axon-bearing amacrine cells in the dark-adapted rabbit retina. Vis. Neurosci.13, 599–604 (1996). ArticleCAS Google Scholar
Taylor, W. R. TTX attenuates surround inhibition in rabbit retinal ganglion cells. Vis. Neurosci.16, 285–290 (1999). ArticleCAS Google Scholar
Mills, S. L. & Massey, S. C. Morphology of bipolar cells labeled by DAPI in the rabbit retina. J. Comp. Neurol.321, 133–149 (1992). ArticleCAS Google Scholar
Massey, S. C. & Mills, S. L. A calbindin-immunoreactive cone bipolar cell type in the rabbit retina. J. Comp. Neurol.366, 15–33 (1996). ArticleCAS Google Scholar
Brown, S. P. & Masland, R. H. Costratification of a population of bipolar cells with the direction-selective circuitry of the rabbit retina. J. Comp. Neurol.408, 97–106 (1999). ArticleCAS Google Scholar
Sterling, P. in The Synaptic Organization of the Brain (ed. Shepherd, G.) 205–253 (Oxford Univ. Press, Oxford, 1998). Google Scholar
Perlman, I. & Normann, R. A. Light adaptation and sensitivity controlling mechanisms in vertebrate photoreceptors. Prog. Ret. Eye Res.17, 523–563 (1998). ArticleCAS Google Scholar
Witkovsky, P. & Dearry, A. Functional roles of dopamine in the vertebrate retina. Prog. Ret. Res.11, 247–292 (1991). ArticleCAS Google Scholar
Cleland, B. G. & Freeman, A. W. Visual adaptation is highly localized in the cat's retina. J. Physiol. Lond.404, 591–611 (1988). ArticleCAS Google Scholar
Yang, G. & Masland, R. H. Receptive fields and dendritic structure of directionally selective retinal ganglion cells. J. Neurosci.14, 5267–5280 (1994). ArticleCAS Google Scholar
He, S. & Masland, R. H. Retinal direction selectivity after targeted laser ablation of starburst amacrine cells. Nature389, 378–382 (1997). ArticleCAS Google Scholar
Brown, S. P., He, S. & Masland, R. H. Receptive field microstructure and dendritic geometry of retinal ganglion cells. Neuron27, 371–383 (2000). ArticleCAS Google Scholar
Levick, W. R. Another tungsten microelectrode. Med. Biol. Eng.10, 510–515 (1972). ArticleCAS Google Scholar
Zhou, Z. J. & Fain, G. L. Neurotransmitter receptors of starburst amacrine cells in rabbit retinal slices. J. Neurosci.15, 5334–5345 (1995). ArticleCAS Google Scholar
Massey, S. C., Linn, D. M., Kittila, C. A. & Mirza, W. Contributions of GABAA receptors and GABAC receptors to acetylcholine release and directional selectivity in the rabbit retina. Vis. Neurosci.14, 939–948 (1997). ArticleCAS Google Scholar
Park, S. K. & Miller, K. W. Random number generators: good ones are hard to find. Communications ACM31, 1192–1201 (1988). Article Google Scholar
Reid, R. C., Victor, J. D. & Shapley, R. M. The use of m-sequences in the analysis of visual neurons: linear receptive field properties. Vis. Neurosci.14, 1015–1027 (1997). ArticleCAS Google Scholar
De Boer, E. & Kuyper, P. Trigger correlation. IEEE Trans. Biomed. Eng.15, 169–179 (1968). ArticleCAS Google Scholar
DeVries, S. H. & Baylor, D. A. Mosaic arrangement of ganglion cell receptive fields in rabbit retina. J. Neurophysiol.78, 2048–2060 (1997). ArticleCAS Google Scholar
Levick, W. R. Receptive fields and trigger features of ganglion cells in the visual streak of the rabbit's retina. J. Physiol. Lond.188, 285–307 (1967). ArticleCAS Google Scholar
Buhl, E. H. & Peichl, L. Morphology of rabbit retinal ganglion cells projecting to the medial terminal nucleus of the accessory optic system. J. Comp. Neurol.253, 163–174 (1986). ArticleCAS Google Scholar
Peichl, L., Buhl, E. H. & Boycott, B. B. Alpha ganglion cells in the rabbit retina. J. Comp. Neurol.263, 25–41 (1987). ArticleCAS Google Scholar
Amthor, F. R., Takahashi, E. S. & Oyster, C. W. Morphologies of rabbit retinal ganglion cells with complex receptive fields. J. Comp. Neurol.280, 97–121 (1989). ArticleCAS Google Scholar
Amthor, F. R., Takahashi, E. S. & Oyster, C. W. Morphologies of rabbit retinal ganglion cells with concentric receptive fields. J. Comp. Neurol.280, 72–96 (1989). ArticleCAS Google Scholar
He, S. & Masland, R. H. ON direction-selective ganglion cells in the rabbit retina: dendritic morphology and pattern of fasciculation. Vis. Neurosci.15, 369–375 (1998). Article Google Scholar