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How We See Black and White: The Role of Midget Ganglion Cells
According to classical opponent color theory, hue sensations are mediated by spectrally opponent neurons that are excited by some wavelengths of light and inhibited by others, while black-and-white sensations are mediated by spectrally non-opponent neurons that respond with the same sign to all wave...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294633/ https://www.ncbi.nlm.nih.gov/pubmed/35864822 http://dx.doi.org/10.3389/fnana.2022.944762 |
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author | Rezeanu, Dragos Neitz, Maureen Neitz, Jay |
author_facet | Rezeanu, Dragos Neitz, Maureen Neitz, Jay |
author_sort | Rezeanu, Dragos |
collection | PubMed |
description | According to classical opponent color theory, hue sensations are mediated by spectrally opponent neurons that are excited by some wavelengths of light and inhibited by others, while black-and-white sensations are mediated by spectrally non-opponent neurons that respond with the same sign to all wavelengths. However, careful consideration of the morphology and physiology of spectrally opponent L vs. M midget retinal ganglion cells (RGCs) in the primate retina indicates that they are ideally suited to mediate black-and-white sensations and poorly suited to mediate color. Here we present a computational model that demonstrates how the cortex could use unsupervised learning to efficiently separate the signals from L vs. M midget RGCs into distinct signals for black and white based only correlation of activity over time. The model also reveals why it is unlikely that these same ganglion cells could simultaneously mediate our perception of red and green, and shows how, in theory, a separate small population of midget RGCs with input from S, M, and L cones would be ideally suited to mediating hue perception. |
format | Online Article Text |
id | pubmed-9294633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92946332022-07-20 How We See Black and White: The Role of Midget Ganglion Cells Rezeanu, Dragos Neitz, Maureen Neitz, Jay Front Neuroanat Neuroanatomy According to classical opponent color theory, hue sensations are mediated by spectrally opponent neurons that are excited by some wavelengths of light and inhibited by others, while black-and-white sensations are mediated by spectrally non-opponent neurons that respond with the same sign to all wavelengths. However, careful consideration of the morphology and physiology of spectrally opponent L vs. M midget retinal ganglion cells (RGCs) in the primate retina indicates that they are ideally suited to mediate black-and-white sensations and poorly suited to mediate color. Here we present a computational model that demonstrates how the cortex could use unsupervised learning to efficiently separate the signals from L vs. M midget RGCs into distinct signals for black and white based only correlation of activity over time. The model also reveals why it is unlikely that these same ganglion cells could simultaneously mediate our perception of red and green, and shows how, in theory, a separate small population of midget RGCs with input from S, M, and L cones would be ideally suited to mediating hue perception. Frontiers Media S.A. 2022-07-05 /pmc/articles/PMC9294633/ /pubmed/35864822 http://dx.doi.org/10.3389/fnana.2022.944762 Text en Copyright © 2022 Rezeanu, Neitz and Neitz. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroanatomy Rezeanu, Dragos Neitz, Maureen Neitz, Jay How We See Black and White: The Role of Midget Ganglion Cells |
title | How We See Black and White: The Role of Midget Ganglion Cells |
title_full | How We See Black and White: The Role of Midget Ganglion Cells |
title_fullStr | How We See Black and White: The Role of Midget Ganglion Cells |
title_full_unstemmed | How We See Black and White: The Role of Midget Ganglion Cells |
title_short | How We See Black and White: The Role of Midget Ganglion Cells |
title_sort | how we see black and white: the role of midget ganglion cells |
topic | Neuroanatomy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294633/ https://www.ncbi.nlm.nih.gov/pubmed/35864822 http://dx.doi.org/10.3389/fnana.2022.944762 |
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