Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network

Optical imaging of dendritic calcium signals provided evidence of starburst amacrine cells exhibiting calcium bias to somatofugal motion. In contrast, it has been impractical to use a dual-patch clamp technique to record membrane potentials from both proximal dendrites and distal varicosities of sta...

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Main Author: Poznanski, R.R.
Format: Article
Published: Imperial College Press 2010
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Online Access:http://eprints.um.edu.my/12467/
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spelling my.um.eprints.124672015-01-29T02:56:56Z http://eprints.um.edu.my/12467/ Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network Poznanski, R.R. R Medicine Optical imaging of dendritic calcium signals provided evidence of starburst amacrine cells exhibiting calcium bias to somatofugal motion. In contrast, it has been impractical to use a dual-patch clamp technique to record membrane potentials from both proximal dendrites and distal varicosities of starburst amacrine cells in order to unequivocally prove that they are directionally sensitive to voltage, as was first suggested almost two decades ago. This paper aims to extend the passive cable model to an active cable model of a starburst amacrine cell that is intrinsically dependent on the electrical properties of starburst amacrine cells, whose various macroscopic currents are described quantitatively. The coupling between voltage and calcium just below the membrane results in a voltage-calcium system of coupled nonlinear Volterra integral equations whose solutions must be integrated into a prescribed model for example, for a synaptic couplet of starburst amacrine cells. Networks of starburst amacrine cells play a fundamental role in the retinal circuitry underlying directional selectivity. It is suggested that the dendritic plexus of starburst amacrine cells provides the substrate for the property of directional selectivity, while directional selectivity is a property of the exclusive layerings and confinement of their interconnections within the sublaminae of the inner plexiform layer involving cone bipolar cells and directionally selective ganglion cells. Imperial College Press 2010 Article PeerReviewed Poznanski, R.R. (2010) Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network. Journal of Integrative Neuroscience, 9 (3). pp. 299-335.
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic R Medicine
spellingShingle R Medicine
Poznanski, R.R.
Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network
description Optical imaging of dendritic calcium signals provided evidence of starburst amacrine cells exhibiting calcium bias to somatofugal motion. In contrast, it has been impractical to use a dual-patch clamp technique to record membrane potentials from both proximal dendrites and distal varicosities of starburst amacrine cells in order to unequivocally prove that they are directionally sensitive to voltage, as was first suggested almost two decades ago. This paper aims to extend the passive cable model to an active cable model of a starburst amacrine cell that is intrinsically dependent on the electrical properties of starburst amacrine cells, whose various macroscopic currents are described quantitatively. The coupling between voltage and calcium just below the membrane results in a voltage-calcium system of coupled nonlinear Volterra integral equations whose solutions must be integrated into a prescribed model for example, for a synaptic couplet of starburst amacrine cells. Networks of starburst amacrine cells play a fundamental role in the retinal circuitry underlying directional selectivity. It is suggested that the dendritic plexus of starburst amacrine cells provides the substrate for the property of directional selectivity, while directional selectivity is a property of the exclusive layerings and confinement of their interconnections within the sublaminae of the inner plexiform layer involving cone bipolar cells and directionally selective ganglion cells.
format Article
author Poznanski, R.R.
author_facet Poznanski, R.R.
author_sort Poznanski, R.R.
title Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network
title_short Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network
title_full Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network
title_fullStr Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network
title_full_unstemmed Cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network
title_sort cellular inhibitory behavior underlying the formation of retinal direction selectivity in the starburst network
publisher Imperial College Press
publishDate 2010
url http://eprints.um.edu.my/12467/
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score 13.211869