Abstract

The retinal cone bipolar cells are interneurons which receive inputs from cone photoreceptors and send outputs to retinal ganglion cells. Several subtypes of bipolar cells have been identified by morphology and electrophysiology in the mammalian retina, which convey distinct visual information to higher order neurons in parallel. The neural circuit in the retina not only converts light information to neural . information, but also performs visual information preprocessing that has not yet been fully understood. Recently, it has been revealed that the neural circuits in retinas of higher vertebrates, such as mammals and primates, have various biophysical properties arising from being composed of ionic channels, ionic pumps, and neurotransmitter receptors. Analysis using a mathematical model based on their ionic mechanisms is essential to understand the visual information processing in the retinal neural circuit of the higher vertebrates.
 The cones and the bipolar cells respond to continuous variation of light with a graded potential, in an analog manner. Especially, glutamate is continuously released from a cone synapse in the dark and is decreased by hyperpolarization of the cone that receives the light stimulus. The alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and kainate type ionotropic glutamate receptors (iGluRs) of the OFF type bipolar cells (OFF-BCs) exhibit partial or nearly complete desensitization in the sustained presence of glutamate. In the dark, glutamate concentration in the synaptic cleft of the cone pedicle rises to 0.1–0.5 mM.5,6 The baseline glutamate concentration depends on a sustained hyperpolarization of the cone by light. Thus, for understanding the working of the OFF-BCs, it is important to elucidate the mechanisms of synaptic transmission from cones to OFF-BCs via iGluRs, which undergo desensitization in the various background light conditions. Furthermore, there are various kinds of ionic channels in OFF-BCs that mediate membrane potential responses. It is considered that information transmitted from cones to OFF-BCs is modulated by the intrinsic ionic currents. We analyzed how ionic currents of OFF-BCs contribute to the transmission of light responses by developing a mathematical model.

Highlights

  • Background and purposeThe retinal cone bipolar cells are interneurons which receive inputs from cone photoreceptors and send outputs to retinal ganglion cells

  • Vpp to low-frequency inputs were decreased with increased maximal conductance of iKv and ih (Fig. 2, open circles in right panel), when at least one of the iKv or ih was activated at VBC. These results suggest that transmission of temporal low-frequency signals in OFF type bipolar cells (OFF-BCs) depends on the baseline glutamate concentrations in the postsynaptic site, which are mainly controlled by the mean light intensity

  • The results suggest that the difference of the frequency characteristics of OFF-BC response was produced by the ionotropic glutamate receptors (iGluRs) current and their somatic ionic currents

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Summary

Introduction

Background and purposeThe retinal cone bipolar cells are interneurons which receive inputs from cone photoreceptors and send outputs to retinal ganglion cells. Several subtypes of bipolar cells have been identified by morphology and electrophysiology in the mammalian retina, which convey distinct visual information to higher order neurons in parallel.[1] The neural circuit in the retina converts light information to neural information, and performs visual information preprocessing that has not yet been fully understood. It has been revealed that the neural circuits in retinas of higher vertebrates, such as mammals and primates, have various biophysical properties arising from being composed of ionic channels, ionic pumps, and neurotransmitter receptors. Analysis using a mathematical model based on their ionic mechanisms is essential to understand the visual information processing in the retinal neural circuit of the higher vertebrates. The cones and the bipolar cells respond to continuous variation of light with a graded potential, in an analog manner. Glutamate is continuously released from a cone synapse in the dark and is decreased by hyperpolarization of the

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