AMPA receptors at ribbon synapses in the mammalian retina: kinetic models and molecular identity
Autor: | Margaret Lin Veruki, Bas-Jan Zandt, Eirik Madsen, Espen Hartveit, Svein Harald Mørkve, Aurea F. Castilho |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Histology Patch-Clamp Techniques Action Potentials Glutamic Acid AMPA receptor Biology Neurotransmission Ribbon synapse In Vitro Techniques Synaptic Transmission Retina Amacrine cells 03 medical and health sciences 0302 clinical medicine Postsynaptic potential medicine Image Processing Computer-Assisted Animals Kinetic scheme Receptors AMPA Long-term depression Neurons Stochastic Processes Microscopy Confocal Dose-Response Relationship Drug General Neuroscience Glutamate receptors Phosphoproteins Electric Stimulation Rats DNA-Binding Proteins Alcohol Oxidoreductases Kinetics 030104 developmental biology medicine.anatomical_structure Silent synapse Synapses Female sense organs Synaptic signaling Patch clamp Anatomy Neuroscience Co-Repressor Proteins Disks Large Homolog 4 Protein 030217 neurology & neurosurgery |
Zdroj: | Brain Structure and Function 769–804 |
ISSN: | 1863-2661 |
Popis: | In chemical synapses, neurotransmitter molecules released from presynaptic vesicles activate populations of postsynaptic receptors that vary in functional properties depending on their subunit composition. Differential expression and localization of specific receptor subunits are thought to play fundamental roles in signal processing, but our understanding of how that expression is adapted to the signal processing in individual synapses and microcircuits is limited. At ribbon synapses, glutamate release is independent of action potentials and characterized by a high and rapidly changing rate of release. Adequately translating such presynaptic signals into postsynaptic electrical signals poses a considerable challenge for the receptor channels in these synapses. Here, we investigated the functional properties of AMPA receptors of AII amacrine cells in rat retina that receive input at spatially segregated ribbon synapses from OFF-cone and rod bipolar cells. Using patch-clamp recording from outside-out patches, we measured the concentration dependence of response amplitude and steady-state desensitization, the single-channel conductance and the maximum open probability. The GluA4 subunit seems critical for the functional properties of AMPA receptors in AII amacrines and immunocytochemical labeling suggested that GluA4 is located at synapses made by both OFF-cone bipolar cells and rod bipolar cells. Finally, we used a series of experimental observables to develop kinetic models for AII amacrine AMPA receptors and subsequently used the models to explore the behavior of the receptors and responses generated by glutamate concentration profiles mimicking those occurring in synapses. These models will facilitate future in silico modeling of synaptic signaling and processing in AII amacrine cells. acceptedVersion |
Databáze: | OpenAIRE |
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