A Dendrite-Autonomous Mechanism for Direction Selectivity in Retinal Starburst Amacrine Cells

Detection of image motion direction begins in the retina, with starburst amacrine cells (SACs) playing a major role. SACs generate larger dendritic Ca2+ signals when motion is from their somata towards their dendritic tips than for motion in the opposite direction. To study the mechanisms underlying the computation of direction selectivity (DS) in SAC dendrites, electrical responses to expanding and contracting circular wave visual stimuli were measured via somatic whole-cell recordings and quantified using Fourier analysis. Fundamental and, especially, harmonic frequency components were larger for expanding stimuli. This DS persists in the presence of GABA and glycine receptor antagonists, suggesting that inhibitory network interactions are not essential. The presence of harmonics indicates nonlinearity, which, as the relationship between harmonic amplitudes and holding potential indicates, is likely due to the activation of voltage-gated channels. [Ca2+] changes in SAC dendrites evoked by voltage steps and monitored by two-photon microscopy suggest that the distal dendrite is tonically depolarized relative to the soma, due in part to resting currents mediated by tonic glutamatergic synaptic input, and that high-voltage–activated Ca2+ channels are active at rest. Supported by compartmental modeling, we conclude that dendritic DS in SACs can be computed by the dendrites themselves, relying on voltage-gated channels and a dendritic voltage gradient, which provides the spatial asymmetry necessary for direction discrimination.

[1]  F. Wilcoxon Individual Comparisons by Ranking Methods , 1945 .

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

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

[4]  Wilfrid Rall,et al.  Theoretical significance of dendritic trees for neuronal input-output relations , 1964 .

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

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

[7]  H. J. Wyatt,et al.  Specific effects of neurotransmitter antagonists on ganglion cells in rabbit retina. , 1976, Science.

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

[9]  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.

[10]  A. Hodgkin,et al.  A surprising property of electrical spread in the network of rods in the turtle's retina , 1978, Nature.

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

[12]  R. Fettiplace,et al.  An electrical tuning mechanism in turtle cochlear hair cells , 1981, The Journal of physiology.

[13]  E Neher,et al.  A patch‐clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine. , 1982, The Journal of physiology.

[14]  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.

[15]  S. Bloomfield,et al.  Electroanatomy of a unique amacrine cell in the rabbit retina. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

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

[17]  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.

[18]  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.

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

[20]  M. Nowycky,et al.  Kinetic and pharmacological properties distinguishing three types of calcium currents in chick sensory neurones. , 1987, The Journal of physiology.

[21]  Christopher Brandon,et al.  Cholinergic neurons in the rabbit retina: dendritic branching and ultrastructural connectivity , 1987, Brain Research.

[22]  T. Millar,et al.  Cholinergic amacrine cells in the rabbit retina synapse onto other cholinergic amacrine cells , 1987, Neuroscience Letters.

[23]  Alexander Borst,et al.  Principles of visual motion detection , 1989, Trends in Neurosciences.

[24]  Shaun P. Collin,et al.  Dendritic Relationships between Cholinergic Amacrine Cells and Direction-Selective Retinal Ganglion Cells , 1989 .

[25]  W. Reichardt,et al.  Computational structure of a biological motion-detection system as revealed by local detector analysis in the fly's nervous system. , 1989, Journal of the Optical Society of America. A, Optics and image science.

[26]  W. G. Owen,et al.  Spatial organization of the bipolar cell's receptive field in the retina of the tiger salamander. , 1990, The Journal of physiology.

[27]  W. Denk,et al.  Two-photon laser scanning fluorescence microscopy. , 1990, Science.

[28]  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.

[29]  D. O'Malley,et al.  Co-release of acetylcholine and GABA by the starburst amacrine cells , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[30]  N. Grzywacz,et al.  A model of the directional selectivity circuit in retina: transformations by neurons singly and in concert , 1992 .

[31]  R R Poznanski,et al.  Modelling the electrotonic structure of starburst amacrine cells in the rabbit retina: A functional interpretation of dendritic morphology , 1992, Bulletin of mathematical biology.

[32]  T. Narahashi,et al.  Differential properties of tetrodotoxin-sensitive and tetrodotoxin- resistant sodium channels in rat dorsal root ganglion neurons , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

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

[34]  E. V. Famiglietti,et al.  Dendritic Co‐stratification of ON and ON‐OFF directionally selective ganglion cells with starburst amacrine cells in rabbit retina , 1992, The Journal of comparative neurology.

[35]  H. Wässle,et al.  Cholinergic amacrine cells of the rat retina express the δ-subunit of the GABAA-receptor , 1993, Neuroscience Letters.

[36]  H. Wässle,et al.  Pharmacology of GABA receptor CI− channels in rat retinal bipolar cells , 1993, Nature.

[37]  R. Tsien,et al.  Distinctive pharmacology and kinetics of cloned neuronal Ca2+ channels and their possible counterparts in mammalian CNS neurons , 1993, Neuropharmacology.

[38]  M. Adams,et al.  Calcium channel diversity and neurotransmitter release: the omega-conotoxins and omega-agatoxins. , 1994, Annual review of biochemistry.

[39]  G. Fain,et al.  Neurotransmitter receptors of starburst amacrine cells in rabbit retinal slices , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[40]  H. Wässle,et al.  Receptive Field Properties of Starburst Cholinergic Amacrine Cells in the Rabbit Retina , 1995, The European journal of neuroscience.

[41]  R. Jensen Effects of Ca2+ channel blockers on directional selectivity of rabbit retinal ganglion cells. , 1995, Journal of neurophysiology.

[42]  H Barlow,et al.  Intraneuronal information processing, directional selectivity and memory for spatio-temporal sequences. , 1996, Network.

[43]  R. Masland,et al.  Responses to light of starburst amacrine cells. , 1996, Journal of neurophysiology.

[44]  H. Wässle,et al.  Immunocytochemical Localization of the GABACReceptor ρ Subunits in the Mammalian Retina , 1996, The Journal of Neuroscience.

[45]  J. Ruppersberg Ion Channels in Excitable Membranes , 1996 .

[46]  T. Velte,et al.  Spiking and nonspiking models of starburst amacrine cells in the rabbit retina , 1997, Visual Neuroscience.

[47]  S. Massey,et al.  Contributions of GABAA receptors and GABAC receptors to acetylcholine release and directional selectivity in the rabbit retina , 1997, Visual Neuroscience.

[48]  F. Amthor,et al.  Non-monotonic contrast behavior in directionally selective ganglion cells and evidence for its dependence on their GABAergic input , 1998, Visual Neuroscience.

[49]  P. Detwiler,et al.  Optical recording of light-evoked calcium signals in the functionally intact retina. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[50]  Vivien A. Casagrande,et al.  Biophysics of Computation: Information Processing in Single Neurons , 1999 .

[51]  K. Matsushita Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)) , 2000 .

[52]  C. Fletcher,et al.  Reduced Voltage Sensitivity of Activation of P/Q-Type Ca2+ Channels is Associated with the Ataxic Mouse MutationRolling Nagoya (tgrol ) , 2000, The Journal of Neuroscience.

[53]  A. Dolphin,et al.  Functional expression and characterization of a voltage-gated CaV1.3 (alpha1D) calcium channel subunit from an insulin-secreting cell line. , 2001, Molecular endocrinology.

[54]  E. Lakatta,et al.  Ion concentration-dependence of rat cardiac unitary L-type calcium channel conductance. , 2001, Biophysical journal.

[55]  E. Cohen Voltage-gated calcium and sodium currents of starburst amacrine cells in the rabbit retina , 2001, Visual Neuroscience.

[56]  Lyle J. Borg-Graham,et al.  The computation of directional selectivity in the retina occurs presynaptic to the ganglion cell , 2001, Nature Neuroscience.

[57]  J. Zanker,et al.  Motion vision : computational, neural, and ecological constraints , 2001 .

[58]  W. R. Levick,et al.  Direction-Selective Ganglion Cells in the Retina , 2001 .

[59]  P. Detwiler,et al.  Directionally selective calcium signals in dendrites of starburst amacrine cells , 2002, Nature.

[60]  W. R. Taylor,et al.  Diverse Synaptic Mechanisms Generate Direction Selectivity in the Rabbit Retina , 2002, The Journal of Neuroscience.

[61]  S. Borges,et al.  Na(+)-Ca(2+) exchanger controls the gain of the Ca(2+) amplifier in the dendrites of amacrine cells. , 2002, Journal of neurophysiology.

[62]  Frank S. Werblin,et al.  Mechanisms and circuitry underlying directional selectivity in the retina , 2002, Nature.

[63]  S. Massey,et al.  AMPA receptors mediate acetylcholine release from starburst amacrine cells in the rabbit retina , 2003, The Journal of comparative neurology.

[64]  S. Mangel,et al.  Cation–chloride cotransporters mediate neural computation in the retina , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[65]  W. R. Taylor,et al.  New directions in retinal research , 2003, Trends in Neurosciences.

[66]  Seunghoon Lee,et al.  A Developmental Switch in the Excitability and Function of the Starburst Network in the Mammalian Retina , 2004, Neuron.

[67]  B. Sakmann,et al.  Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches , 1981, Pflügers Archiv.

[68]  J. J. Tukker,et al.  Direction selectivity in a model of the starburst amacrine cell , 2004, Visual Neuroscience.

[69]  Bernardo Rudy,et al.  A Unique Role for Kv3 Voltage-Gated Potassium Channels in Starburst Amacrine Cell Signaling in Mouse Retina , 2004, The Journal of Neuroscience.

[70]  Diane Lipscombe,et al.  L-type calcium channels: the low down. , 2004, Journal of neurophysiology.

[71]  Nicholas Oesch,et al.  Direction-Selective Dendritic Action Potentials in Rabbit Retina , 2005, Neuron.

[72]  S. Borges,et al.  Calcium from internal stores triggers GABA release from retinal amacrine cells. , 2005, Journal of neurophysiology.

[73]  M. London,et al.  Dendritic computation. , 2005, Annual review of neuroscience.

[74]  Wenzhi Sun,et al.  Identification of ON–OFF direction‐selective ganglion cells in the mouse retina , 2005, The Journal of physiology.

[75]  W. Sather Selective Permeability of Voltage-Gated Calcium Channels , 2005 .

[76]  M. Slaughter,et al.  Effects of GABA receptor antagonists on retinal glycine receptors and on homomeric glycine receptor alpha subunits. , 2005, Journal of neurophysiology.

[77]  Andrey V Dmitriev,et al.  Dendritic compartmentalization of chloride cotransporters underlies directional responses of starburst amacrine cells in retina , 2006, Proceedings of the National Academy of Sciences.

[78]  F. Werblin,et al.  Symmetric interactions within a homogeneous starburst cell network can lead to robust asymmetries in dendrites of starburst amacrine cells. , 2006, Journal of neurophysiology.

[79]  Seunghoon Lee,et al.  The Synaptic Mechanism of Direction Selectivity in Distal Processes of Starburst Amacrine Cells , 2006, Neuron.

[80]  Shelley I. Fried,et al.  Image Processing: How the Retina Detects the Direction of Image Motion , 2007, Current Biology.