Literature DB >> 9862914

Transmitter concentration at a three-dimensional synapse.

R Rao-Mirotznik1, G Buchsbaum, P Sterling.   

Abstract

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.

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Year:  1998        PMID: 9862914     DOI: 10.1152/jn.1998.80.6.3163

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  24 in total

1.  A clockwork hypothesis: synaptic release by rod photoreceptors must be regular.

Authors:  Stan Schein; Kareem M Ahmad
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Review 2.  Synaptic transmission at retinal ribbon synapses.

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3.  Efficiency of synaptic transmission of single-photon events from rod photoreceptor to rod bipolar dendrite.

Authors:  Stan Schein; Kareem M Ahmad
Journal:  Biophys J       Date:  2006-08-18       Impact factor: 4.033

Review 4.  The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease.

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Review 5.  Kinetics of synaptic transmission at ribbon synapses of rods and cones.

Authors:  Wallace B Thoreson
Journal:  Mol Neurobiol       Date:  2007-07-10       Impact factor: 5.590

Review 6.  Connectomics of synaptic microcircuits: lessons from the outer retina.

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Review 7.  Voltage-Gated Calcium Channels: Key Players in Sensory Coding in the Retina and the Inner Ear.

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Review 8.  The excitatory neurotransmitter glutamate stimulates DNA repair to increase neuronal resiliency.

Authors:  Jenq-Lin Yang; Peter Sykora; David M Wilson; Mark P Mattson; Vilhelm A Bohr
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9.  Quantal mEPSCs and residual glutamate: how horizontal cell responses are shaped at the photoreceptor ribbon synapse.

Authors:  Lucia Cadetti; Theodore M Bartoletti; Wallace B Thoreson
Journal:  Eur J Neurosci       Date:  2008-05       Impact factor: 3.386

10.  Properties of ribbon and non-ribbon release from rod photoreceptors revealed by visualizing individual synaptic vesicles.

Authors:  Minghui Chen; Matthew J Van Hook; David Zenisek; Wallace B Thoreson
Journal:  J Neurosci       Date:  2013-01-30       Impact factor: 6.167

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