Abstract

Retinal ganglion cells (RGCs) display differences in their morphology and intrinsic electrophysiology. The goal of this study is to characterize the ionic currents that explain the behavior of ON and OFF RGCs and to explore if all morphological types of RGCs exhibit the phenomena described in electrophysiological data. We extend our previous single compartment cell models of ON and OFF RGCs to more biophysically realistic multicompartment cell models and investigate the effect of cell morphology on intrinsic electrophysiological properties. The membrane dynamics are described using the Hodgkin - Huxley type formalism. A subset of published patch-clamp data from isolated intact mouse retina is used to constrain the model and another subset is used to validate the model. Two hundred morphologically distinct ON and OFF RGCs are simulated with various densities of ionic currents in different morphological neuron compartments. Our model predicts that the differences between ON and OFF cells are explained by the presence of the low voltage activated calcium current in OFF cells and absence of such in ON cells. Our study shows through simulation that particular morphological types of RGCs are capable of exhibiting the full range of phenomena described in recent experiments. Comparisons of outputs from different cells indicate that the RGC morphologies that best describe recent experimental results are ones that have a larger ratio of soma to total surface area.

Highlights

  • Photoreceptor cells convert light energy into signals that are transmitted to bipolar cells

  • We propose that not all morphological types of Retinal ganglion cells (RGCs) exhibit the phenomena described by Margolis and Detwiler (2007) and show that this is supported by simulations

  • We present realistic, morphologically correct models of 200 ON and OFF RGCs, and test ionic channel densities in morphological compartments that are necessary to capture experimentally recorded phenomena described by Margolis and Detwiler (2007)

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Summary

Introduction

Photoreceptor cells convert light energy into signals that are transmitted to bipolar cells. Bipolar cells are divided into two types that respond to either increments or decrements in light intensity. Retinal ganglion cells (RGCs) are the sole output neurons of the retina. They convert synaptic input from bipolar and other types of inner retinal neurons into signals that carry visual information to the brain. RGCs that respond with increasing spiking frequency to light increments are called ON RGCs. RGCs that increase their spiking frequency with light decrements are called OFF RGCs. OFF-transient cells (OFF T RGCs) are quiet in darkness and have transient spikes at light offset.

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