How We See Black and White: The Role of Midget Ganglion Cells.
black-and-white vision
color vision
computational neuroscience
midget ganglion cell
primate retina
retinal ganglion cell (RGC)
Journal
Frontiers in neuroanatomy
ISSN: 1662-5129
Titre abrégé: Front Neuroanat
Pays: Switzerland
ID NLM: 101477943
Informations de publication
Date de publication:
2022
2022
Historique:
received:
15
05
2022
accepted:
17
06
2022
entrez:
22
7
2022
pubmed:
23
7
2022
medline:
23
7
2022
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 35864822
doi: 10.3389/fnana.2022.944762
pmc: PMC9294633
doi:
Types de publication
Journal Article
Langues
eng
Pagination
944762Informations de copyright
Copyright © 2022 Rezeanu, Neitz and Neitz.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
Neuron. 2018 Mar 21;97(6):1327-1340.e4
pubmed: 29503188
Elife. 2020 Feb 24;9:
pubmed: 32091390
Psychol Rev. 1957 Nov;64, Part 1(6):384-404
pubmed: 13505974
J Neurosci. 2020 Oct 14;40(42):8132-8148
pubmed: 33009001
Vision Res. 2003 May;43(10):1211-22
pubmed: 12705960
Proc Biol Sci. 2012 Jun 22;279(1737):2289-98
pubmed: 22456882
J Physiol. 1988 Oct;404:323-47
pubmed: 3253435
J Opt Soc Am A Opt Image Sci Vis. 2014 Apr 1;31(4):A195-207
pubmed: 24695170
Science. 1979 Aug 10;205(4406):587-9
pubmed: 109925
PLoS One. 2014 Feb 20;9(2):e88963
pubmed: 24586460
Nat Neurosci. 2021 Sep;24(9):1280-1291
pubmed: 34341586
J Comp Neurol. 2020 Jun 15;528(9):1588-1598
pubmed: 31845339
Eye (Lond). 2017 Feb;31(2):286-300
pubmed: 27935605
Vision Res. 1983;23(12):1495-500
pubmed: 6666050
Sci Adv. 2016 Sep 14;2(9):e1600797
pubmed: 27652339
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2545-9
pubmed: 3470811
J Opt Soc Am A Opt Image Sci Vis. 2014 Apr 1;31(4):A189-94
pubmed: 24695169
J Physiol. 1962 Jan;160:106-54
pubmed: 14449617
Neuron. 2002 Aug 15;35(4):783-92
pubmed: 12194876
J Vis. 2002;2(8):531-42
pubmed: 12678637
Neuron. 1999 Oct;24(2):313-21
pubmed: 10571226
J Opt Soc Am. 1966 Jul;56(7):966-77
pubmed: 4959282
Nat Rev Neurosci. 2007 Apr;8(4):276-86
pubmed: 17375040
J Opt Soc Am A Opt Image Sci Vis. 2005 Oct;22(10):2013-33
pubmed: 16277273
Crit Rev Neurobiol. 1988;3(4):333-400
pubmed: 3048707
J Vis. 2016 Jun 1;16(8):18
pubmed: 27366885
J Opt Soc Am. 1976 Jul;66(7):709-17
pubmed: 978286
J Opt Soc Am A Opt Image Sci Vis. 2020 Apr 1;37(4):A244-A254
pubmed: 32400553
J Neurophysiol. 1966 Nov;29(6):1115-56
pubmed: 4961644
J Neurosci. 2008 Apr 9;28(15):4078-87
pubmed: 18400907
Vision Res. 1993 May;33(8):1053-65
pubmed: 8506645
Vision Res. 1979;19(4):441-9
pubmed: 112776