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Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex?

It has been argued that the emergence of roughly periodic orientation preference maps (OPMs) in the primary visual cortex (V1) of carnivores and primates can be explained by a so-called statistical connectivity model. This model assumes that input to V1 neurons is dominated by feed-forward projectio...

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Autores principales: Schottdorf, Manuel, Eglen, Stephen J., Wolf, Fred, Keil, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901677/
https://www.ncbi.nlm.nih.gov/pubmed/24475081
http://dx.doi.org/10.1371/journal.pone.0086139
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author Schottdorf, Manuel
Eglen, Stephen J.
Wolf, Fred
Keil, Wolfgang
author_facet Schottdorf, Manuel
Eglen, Stephen J.
Wolf, Fred
Keil, Wolfgang
author_sort Schottdorf, Manuel
collection PubMed
description It has been argued that the emergence of roughly periodic orientation preference maps (OPMs) in the primary visual cortex (V1) of carnivores and primates can be explained by a so-called statistical connectivity model. This model assumes that input to V1 neurons is dominated by feed-forward projections originating from a small set of retinal ganglion cells (RGCs). The typical spacing between adjacent cortical orientation columns preferring the same orientation then arises via Moiré-Interference between hexagonal ON/OFF RGC mosaics. While this Moiré-Interference critically depends on long-range hexagonal order within the RGC mosaics, a recent statistical analysis of RGC receptive field positions found no evidence for such long-range positional order. Hexagonal order may be only one of several ways to obtain spatially repetitive OPMs in the statistical connectivity model. Here, we investigate a more general requirement on the spatial structure of RGC mosaics that can seed the emergence of spatially repetitive cortical OPMs, namely that angular correlations between so-called RGC dipoles exhibit a spatial structure similar to that of OPM autocorrelation functions. Both in cat beta cell mosaics as well as primate parasol receptive field mosaics we find that RGC dipole angles are spatially uncorrelated. To help assess the level of these correlations, we introduce a novel point process that generates mosaics with realistic nearest neighbor statistics and a tunable degree of spatial correlations of dipole angles. Using this process, we show that given the size of available data sets, the presence of even weak angular correlations in the data is very unlikely. We conclude that the layout of ON/OFF ganglion cell mosaics lacks the spatial structure necessary to seed iso-orientation domains in the primary visual cortex.
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spelling pubmed-39016772014-01-28 Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex? Schottdorf, Manuel Eglen, Stephen J. Wolf, Fred Keil, Wolfgang PLoS One Research Article It has been argued that the emergence of roughly periodic orientation preference maps (OPMs) in the primary visual cortex (V1) of carnivores and primates can be explained by a so-called statistical connectivity model. This model assumes that input to V1 neurons is dominated by feed-forward projections originating from a small set of retinal ganglion cells (RGCs). The typical spacing between adjacent cortical orientation columns preferring the same orientation then arises via Moiré-Interference between hexagonal ON/OFF RGC mosaics. While this Moiré-Interference critically depends on long-range hexagonal order within the RGC mosaics, a recent statistical analysis of RGC receptive field positions found no evidence for such long-range positional order. Hexagonal order may be only one of several ways to obtain spatially repetitive OPMs in the statistical connectivity model. Here, we investigate a more general requirement on the spatial structure of RGC mosaics that can seed the emergence of spatially repetitive cortical OPMs, namely that angular correlations between so-called RGC dipoles exhibit a spatial structure similar to that of OPM autocorrelation functions. Both in cat beta cell mosaics as well as primate parasol receptive field mosaics we find that RGC dipole angles are spatially uncorrelated. To help assess the level of these correlations, we introduce a novel point process that generates mosaics with realistic nearest neighbor statistics and a tunable degree of spatial correlations of dipole angles. Using this process, we show that given the size of available data sets, the presence of even weak angular correlations in the data is very unlikely. We conclude that the layout of ON/OFF ganglion cell mosaics lacks the spatial structure necessary to seed iso-orientation domains in the primary visual cortex. Public Library of Science 2014-01-24 /pmc/articles/PMC3901677/ /pubmed/24475081 http://dx.doi.org/10.1371/journal.pone.0086139 Text en © 2014 Schottdorf et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Schottdorf, Manuel
Eglen, Stephen J.
Wolf, Fred
Keil, Wolfgang
Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex?
title Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex?
title_full Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex?
title_fullStr Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex?
title_full_unstemmed Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex?
title_short Can Retinal Ganglion Cell Dipoles Seed Iso-Orientation Domains in the Visual Cortex?
title_sort can retinal ganglion cell dipoles seed iso-orientation domains in the visual cortex?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901677/
https://www.ncbi.nlm.nih.gov/pubmed/24475081
http://dx.doi.org/10.1371/journal.pone.0086139
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