Transmitter concentration at a three-dimensional synapse.

Transmitter concentration at a three-dimensional synapse. J. Neurophysiol. 80: 3163-3172, 1998. At intensities from starlight to 1000-fold brighter, the mammalian rod synapse transmits a binary signal, the capture of 0 or 1 photon. Zero is signified by tonic exocytosis, and 1 is signified by a brief pause. The synapse is three dimensional: vesicles discharge at the apex of a deep cleft created by the invagination of four postsynaptic processes. Two horizontal cell spines bearing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors reach near to the release sites (16 nm), and two bipolar dendrites bearing mGluR6 receptors end far from the release sites (up to 640 nm). We considered two hypotheses for signal transfer: transmitter quanta might be integrated in the cleft and sensed as a steady concentration (high for 0 and low for 1); or quanta might be sensed at the postsynaptic membrane as discrete postsynaptic potentials (PSPs) and integrated within the dendrite. We calculate from a passive diffusion model that the invagination empties rapidly (tau approximately 1.7 ms). Further calculations suggest that a glutamate concentration high enough to hold a bipolar cell in darkness at one end of its response range would require approximately 4,000 vesicles/s. On the other hand, the glutamate pulse from a single vesicle would reach both nearby AMPA receptors (low affinity) and distant mGluR6 receptors (high affinity) at spatiotemporal concentrations matched to their apparent binding affinities. Thus one vesicle could evoke a discrete PSP in all four postsynaptic processes. We calculate from a stochastic model that PSPs could transfer the binary signal at approximately 100 vesicles/s. Thus dendritic integration of unitary PSPs is both plausible and 40-fold more efficient than the alternative mechanism. The rod's deep invagination, rather than serving to pool transmitter, may serve to prevent "spillover" of transmitter to neighboring rods. Spillover, by pooling the noise from neighboring rods, would impair transmission of their binary signals.

[1]  W. Almers,et al.  Transmitter release from synapses: Does a preassembled fusion pore initiate exocytosis? , 1990, Neuron.

[2]  B. Boycott,et al.  Organization of the primate retina: electron microscopy , 1966, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[3]  G Falk,et al.  Responses of rod bipolar cells isolated from dogfish retinal slices to concentration-jumps of glutamate , 1994, Visual Neuroscience.

[4]  D. Kullmann,et al.  Extrasynaptic Glutamate Spillover in the Hippocampus: Dependence on Temperature and the Role of Active Glutamate Uptake , 1997, Neuron.

[5]  M. Barbe Tempting Fate and Commitment in the Developing Forebrain , 1996, Neuron.

[6]  Charles Nicholson,et al.  Ion-selective microelectrodes and diffusion measurements as tools to explore the brain cell microenvironment , 1993, Journal of Neuroscience Methods.

[7]  A. Kaneko,et al.  L-glutamate-induced responses and cGMP-activated channels in three subtypes of retinal bipolar cells dissociated from the cat , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  G. Matthews,et al.  Evidence That Vesicles on the Synaptic Ribbon of Retinal Bipolar Neurons Can Be Rapidly Released , 1996, Neuron.

[9]  G Falk,et al.  Responses of rod‐bipolar cells in the dark‐adapted retina of the dogfish, Scyliorhinus canicula , 1980, The Journal of physiology.

[10]  C. Jahr,et al.  Transporters Buffer Synaptically Released Glutamate on a Submillisecond Time Scale , 1997, The Journal of Neuroscience.

[11]  N. Vardi,et al.  Differential expression of ionotropic glutamate receptor subunits in the outer retina , 1999, The Journal of comparative neurology.

[12]  Peter Sterling,et al.  Parallel Circuits from Cones to the On‐Beta Ganglion Cell , 1992, The European journal of neuroscience.

[13]  J. Eccles,et al.  The relationship between the mode of operation and the dimensions of the junctional regions at synapses and motor end-organs , 1958, Proceedings of the Royal Society of London. Series B - Biological Sciences.

[14]  G. Buchsbaum,et al.  Mammalian rod terminal: Architecture of a binary synapse , 1995, Neuron.

[15]  Pharmacological similarity between the retinal APB receptor and the family of metabotropic glutamate receptors. , 1994, Journal of neurophysiology.

[16]  B. Hille Ionic channels of excitable membranes , 2001 .

[17]  E. Raviola,et al.  Intramembrane organization of specialized contacts in the outer plexiform layer of the retina. A freeze-fracture study in monkeys and rabbits , 1975, The Journal of cell biology.

[18]  F. Orrego,et al.  Glutamate in rat brain cortex synaptic vesicles: influence of the vesicle isolation procedure , 1986, Brain Research.

[19]  C. Karwoski,et al.  Laminar profile of resistivity in frog retina. , 1985, Journal of neurophysiology.

[20]  N. Vardi,et al.  ON cone bipolar cells in rat express the metabotropic receptor mGluR6 , 1997, Visual Neuroscience.

[21]  D. I. Vaney The coupling pattern of axon-bearing horizontal cells in the mammalian retina , 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[22]  Tokuro Suzuki,et al.  Fast and Slow Components of Auditory Brainstem Response , 1984 .

[23]  John Crank,et al.  The Mathematics Of Diffusion , 1956 .

[24]  Shaul Hestrin,et al.  Activation and desensitization of glutamate-activated channels mediating fast excitatory synaptic currents in the visual cortex , 1992, Neuron.

[25]  L. G. Longsworth,et al.  Diffusion Measurements, at 25°, of Aqueous Solutions of Amino Acids, Peptides and Sugars , 1952 .

[26]  G Buchsbaum,et al.  Rate of quantal transmitter release at the mammalian rod synapse. , 1994, Biophysical journal.

[27]  W. Holmes Modeling the effect of glutamate diffusion and uptake on NMDA and non-NMDA receptor saturation. , 1995, Biophysical journal.

[28]  A. Lasansky Organization of the outer synaptic layer in the retina of the larval tiger salamander. , 1973, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[29]  D. Attwell,et al.  The release and uptake of excitatory amino acids. , 1990, Trends in pharmacological sciences.

[30]  P. Sterling,et al.  Foveal Cones form Basal as well as Invaginating Junctions with Diffuse ON Bipolar Cells , 1996, Vision Research.

[31]  H. Barlow,et al.  Responses to single quanta of light in retinal ganglion cells of the cat. , 1971, Vision research.

[32]  P. Witkovsky,et al.  The effects of L-glutamate, AMPA, quisqualate, and kainate on retinal horizontal cells depend on adaptational state: implications for rod- cone interactions , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  L. Trussell,et al.  Delayed clearance of transmitter and the role of glutamate transporters at synapses with multiple release sites , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[34]  W. Almers,et al.  Calcium-triggered exocytosis and endocytosis in an isolated presynaptic cell: Capacitance measurements in saccular hair cells , 1994, Neuron.

[35]  P Sterling,et al.  Microcircuitry of the dark-adapted cat retina: functional architecture of the rod-cone network , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  M. Kavanaugh,et al.  Kinetics of a human glutamate transporter , 1995, Neuron.

[37]  E. A. Schwartz,et al.  Asynchronous transmitter release: control of exocytosis and endocytosis at the salamander rod synapse. , 1996, The Journal of physiology.

[38]  Antonio Malgaroli,et al.  Loose-patch recordings of single quanta at individual hippocampal synapses , 1997, Nature.

[39]  H. V. Gersdorff,et al.  Dynamics of synaptic vesicle fusion and membrane retrieval in synaptic terminals , 1994, Nature.

[40]  Shigetada Nakanishi,et al.  Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells , 1994, Cell.

[41]  G Buchsbaum,et al.  How retinal microcircuits scale for ganglion cells of different size , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[42]  J. Dowling The Retina: An Approachable Part of the Brain , 1988 .

[43]  E. Raviola,et al.  Rod cells dissociated from mature salamander retina: ultrastructure and uptake of horseradish peroxidase , 1985, The Journal of cell biology.

[44]  C. Jahr,et al.  Rapid AMPA receptor desensitization in catfish cone horizontal cells , 1997, Visual Neuroscience.

[45]  L. Missotten,et al.  The ultrastructure of the human retina , 1965 .

[46]  B. Sakmann,et al.  Quantal components of unitary EPSCs at the mossy fibre synapse on CA3 pyramidal cells of rat hippocampus. , 1993, The Journal of physiology.

[47]  P. Sterling,et al.  Architecture of rod and cone circuits to the on-beta ganglion cell , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[48]  Scott Nawy,et al.  Suppression by glutamate of cGMP-activated conductance in retinal bipolar cells , 1990, Nature.

[49]  F. Werblin,et al.  Characterization of the glutamate transporter in retinal cones of the tiger salamander , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[50]  D. Faber,et al.  Synergism at central synapses due to lateral diffusion of transmitter. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[51]  M. Mayer,et al.  Structure-activity relationships for amino acid transmitter candidates acting at N-methyl-D-aspartate and quisqualate receptors , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[52]  B. Sakmann,et al.  Fast and slow components of unitary EPSCs on stellate cells elicited by focal stimulation in slices of rat visual cortex. , 1992, The Journal of physiology.

[53]  G. Westbrook,et al.  The time course of glutamate in the synaptic cleft. , 1992, Science.

[54]  I. Raman,et al.  The mechanism of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor desensitization after removal of glutamate. , 1995, Biophysical journal.

[55]  J. Clements Transmitter timecourse in the synaptic cleft: its role in central synaptic function , 1996, Trends in Neurosciences.

[56]  B. Boycott,et al.  Receptor contacts of horizontal cells in the retina of the domestic cat , 1978, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[57]  D. Baylor,et al.  The photocurrent, noise and spectral sensitivity of rods of the monkey Macaca fascicularis. , 1984, The Journal of physiology.

[58]  W. Almers,et al.  The mechanism of exocytosis during secretion in mast cells. , 1989, Society of General Physiologists series.

[59]  Martin Wilson,et al.  Variation in GABA mini amplitude is the consequence of variation in transmitter concentration , 1995, Neuron.

[60]  L. Trussell,et al.  Glutamate receptor desensitization and its role in synaptic transmission , 1989, Neuron.

[61]  B Sakmann,et al.  Quantal analysis of inhibitory synaptic transmission in the dentate gyrus of rat hippocampal slices: a patch‐clamp study. , 1990, The Journal of physiology.

[62]  G. Falk,et al.  Glutamate receptors of rod bipolar cells are linked to a cyclic GMP cascade via a G-protein , 1990, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[63]  L. M. Wahl,et al.  Monte Carlo simulation of fast excitatory synaptic transmission at a hippocampal synapse. , 1996, Journal of neurophysiology.

[64]  D. Kullmann,et al.  Extrasynaptic Glutamate Diffusion in the Hippocampus: Ultrastructural Constraints, Uptake, and Receptor Activation , 1998, The Journal of Neuroscience.

[65]  J F Ashmore,et al.  An analysis of transmission from cones to hyperpolarizing bipolar cells in the retina of the turtle. , 1983, The Journal of physiology.

[66]  R. Silver,et al.  Estimated conductance of glutamate receptor channels activated during EPSCs at the cerebellar mossy fiber-granule cell synapse , 1993, Neuron.

[67]  P. Maycox,et al.  Synaptic vesicles immunoisolated from rat cerebral cortex contain high levels of glutamate , 1989, Neuron.

[68]  C. Jahr,et al.  Postsynaptic glutamate transport at the climbing fiber-Purkinje cell synapse. , 1997, Science.

[69]  C. Nicholson,et al.  Ion diffusion modified by tortuosity and volume fraction in the extracellular microenvironment of the rat cerebellum. , 1981, The Journal of physiology.

[70]  D. Rossi,et al.  Spillover-Mediated Transmission at Inhibitory Synapses Promoted by High Affinity α6 Subunit GABAA Receptors and Glomerular Geometry , 1998, Neuron.

[71]  Mark C. W. van Rossum,et al.  Noise removal at the rod synapse of mammalian retina , 1998, Visual Neuroscience.

[72]  L. Trussell,et al.  Desensitization of AMPA receptors upon multiquantal neurotransmitter release , 1993, Neuron.

[73]  PR Martin,et al.  Rod bipolar cells in the macaque monkey retina: immunoreactivity and connectivity , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[74]  J. D. Clements,et al.  Activation kinetics reveal the number of glutamate and glycine binding sites on the N-methyl-d-aspartate receptor , 1991, Neuron.