Functional properties of models for direction selectivity in the retina

Poggio and Reichardt (Kybernetik, 13:223–227, 1973) showed that if the average response of a visual system to a moving stimulus is directionally selective, then this sensitivity must be mediated by a nonlinear operation. In particular, it has been proposed that at the behavioral level, motion‐sensitive biological systems are implemented by quadratic nonlinearities (Hassenstein and Reichardt: Z. Naturforsch., 11b:513–524, 1956; van Santen and Sperling: J. Opt. Soc. Am. [A] 1:451–473, 1984; Adelson and Bergen: J. Opt. Soc. Am. [A], 2:284–299, 1985). This paper analyzes theoretically two nonlinear neural mechanisms that possibly underlie retinal direction selectivity and explores the conditions under which they behave as a quadratic nonlinearity. The first mechanism is shunting inhibition (Torre and Poggio: Proc. R. Soc. Lond. [Biol.], 202:409–416, 1978), and the second consists of the linear combination of the outputs of a depolarizing and a hyperpolarizing synapse, followed by a threshold operation. It was found that although sometimes possible, it is in practice hard to approximate the Shunting Inhibition and the Threshold models for direction selectivity by quadratic systems. For instance, the level of the threshold on the Threshold model must be close to the steady‐state level of the cell's combined synaptic input. Furthermore, for both the Shunting and the Threshold models, the approximation by a quadratic system is only possible for a small range of low contrast stimuli and for situations where the rectifications due to the ON–OFF mechanisms, and to the ganglion cells' action potentials, can be linearized. The main question that this paper leaves open is, how do we account for the apparent quadratic properties of motion perception given that the same properties seem so fragile at the single cell level? Finally, as a result of this study, some system analysis experiments were proposed that can distinguish between different instances of the models.

[1]  E. D. Adrian,et al.  The action of light on the eye , 1927 .

[2]  R. S. Burington Handbook of mathematical tables and formulas , 1933 .

[3]  William Albert Hugh Rushton,et al.  Initiation of the Propagated Disturbance , 1937 .

[4]  H. K. Hartline,et al.  THE RECEPTIVE FIELDS OF OPTIC NERVE FIBERS , 1940 .

[5]  D. E. Goldman POTENTIAL, IMPEDANCE, AND RECTIFICATION IN MEMBRANES , 1943, The Journal of general physiology.

[6]  A. Hodgkin,et al.  A quantitative description of membrane current and its application to conduction and excitation in nerve , 1952, The Journal of physiology.

[8]  S. W. Kuffler Discharge patterns and functional organization of mammalian retina. , 1953, Journal of neurophysiology.

[9]  B. Hassenstein,et al.  Systemtheoretische Analyse der Zeit-, Reihenfolgen- und Vorzeichenauswertung bei der Bewegungsperzeption des Rüsselkäfers Chlorophanus , 1956 .

[10]  D. Hubel,et al.  Receptive fields of single neurones in the cat's striate cortex , 1959, The Journal of physiology.

[11]  W. Pitts,et al.  Anatomy and Physiology of Vision in the Frog (Rana pipiens) , 1960, The Journal of general physiology.

[12]  D. Hubel,et al.  Receptive fields of optic nerve fibres in the spider monkey , 1960, The Journal of physiology.

[13]  H. Barlow,et al.  Selective Sensitivity to Direction of Movement in Ganglion Cells of the Rabbit Retina , 1963, Science.

[14]  H. Barlow,et al.  Retinal ganglion cells responding selectively to direction and speed of image motion in the rabbit , 1964, The Journal of physiology.

[15]  H. Barlow,et al.  The mechanism of directionally selective units in rabbit's retina. , 1965, The Journal of physiology.

[16]  J. Stone,et al.  Specialized Receptive Fields of the Cat's Retina , 1966, Science.

[17]  C. R. Michael,et al.  Receptive Fields of Directionally Selective Units in the Optic Nerve of the Ground Squirrel , 1966, Science.

[18]  B. Katz,et al.  A study of synaptic transmission in the absence of nerve impulses , 1967, The Journal of physiology.

[19]  A. Hodgkin,et al.  The frequency of nerve action potentials generated by applied currents , 1967, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[20]  W. Reichardt Movement perception in insects , 1969 .

[21]  H Spekreijse,et al.  Rectification in the goldfish retina: analysis by sinusoidal and auxiliary stimulation. , 1969, Vision research.

[22]  F. Werblin Response of retinal cells to moving spots: intracellular recording in Necturus maculosus. , 1970, Journal of neurophysiology.

[23]  K. Kusano Influence of ionic environment on the relationship between pre- and postsynaptic potentials. , 1970, Journal of neurobiology.

[24]  Bruce W. Knight,et al.  Dynamics of Encoding in a Population of Neurons , 1972, The Journal of general physiology.

[25]  F. Werblin,et al.  Control of Retinal Sensitivity: I. Light and Dark Adaptation of Vertebrate Rods and Cones , 1974 .

[26]  J. Jack,et al.  Electric current flow in excitable cells , 1975 .

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

[28]  P. Schiller,et al.  Quantitative studies of single-cell properties in monkey striate cortex. I. Spatiotemporal organization of receptive fields. , 1976, Journal of neurophysiology.

[29]  W Reichardt,et al.  Visual control of orientation behaviour in the fly: Part II. Towards the underlying neural interactions , 1976, Quarterly Reviews of Biophysics.

[30]  E. Wist,et al.  The spatial frequency effect on perceived velocity , 1976, Vision Research.

[31]  T. Poggio,et al.  The Volterra Representation and the Wiener Expansion: Validity and Pitfalls , 1977 .

[32]  A Kaneko,et al.  Neuronal architecture of on and off pathways to ganglion cells in carp retina. , 1977, Science.

[33]  T. Poggio,et al.  A New Approach to Synaptic Interactions , 1978 .

[34]  J. Caldwell,et al.  Effects of picrotoxin and strychnine on rabbit retinal ganglion cells: lateral interactions for cells with more complex receptive fields. , 1978, The Journal of physiology.

[35]  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.

[36]  P. Marchiafava The responses of retinal ganglion cells to stationary and moving visual stimuli , 1979, Vision Research.

[37]  M. Schetzen The Volterra and Wiener Theories of Nonlinear Systems , 1980 .

[38]  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.

[39]  R. L. Valois,et al.  The orientation and direction selectivity of cells in macaque visual cortex , 1982, Vision Research.

[40]  M. Ariel,et al.  Pharmacological analysis of directionally sensitive rabbit retinal ganglion cells , 1982, The Journal of physiology.

[41]  P. Schwindt,et al.  Factors influencing motoneuron rhythmic firing: results from a voltage-clamp study. , 1982, Journal of neurophysiology.

[42]  T. Poggio,et al.  Nonlinear interactions in a dendritic tree: localization, timing, and role in information processing. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[43]  P. Schwindt,et al.  Active currents in mammalian central neurons , 1983, Trends in Neurosciences.

[44]  E. V. Famiglietti,et al.  On and off pathways through amacrine cells in mammalian retina: The synaptic connections of “starburst” amacrine cells , 1983, Vision Research.

[45]  T. Albright Direction and orientation selectivity of neurons in visual area MT of the macaque. , 1984, Journal of neurophysiology.

[46]  J. van Santen,et al.  Temporal covariance model of human motion perception. , 1984, Journal of the Optical Society of America. A, Optics and image science.

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

[48]  C. Enroth-Cugell,et al.  Chapter 9 Visual adaptation and retinal gain controls , 1984 .

[49]  S. Watanabe,et al.  Synaptic mechanisms of directional selectivity in ganglion cells of frog retina as revealed by intracellular recordings. , 1984, The Japanese journal of physiology.

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

[51]  E H Adelson,et al.  Spatiotemporal energy models for the perception of motion. , 1985, Journal of the Optical Society of America. A, Optics and image science.

[52]  A J Ahumada,et al.  Model of human visual-motion sensing. , 1985, Journal of the Optical Society of America. A, Optics and image science.

[53]  J. van Santen,et al.  Elaborated Reichardt detectors. , 1985, Journal of the Optical Society of America. A, Optics and image science.

[54]  N. Franceschini,et al.  Early processing of colour and motion in a mosaic visual system. , 1985, Neuroscience research. Supplement : the official journal of the Japan Neuroscience Society.

[55]  M. Ariel,et al.  Neurotransmitter inputs to directionally sensitive turtle retinal ganglion cells. , 1985, Journal of neurophysiology.

[56]  R. Shapley,et al.  The primate retina contains two types of ganglion cells, with high and low contrast sensitivity. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[57]  C Koch,et al.  Slow synaptic transmission in frog sympathetic ganglia. , 1986, The Journal of experimental biology.