Cargando…
Orientation-Cue Invariant Population Responses to Contrast-Modulated and Phase-Reversed Contour Stimuli in Macaque V1 and V2
Visual scenes can be readily decomposed into a variety of oriented components, the processing of which is vital for object segregation and recognition. In primate V1 and V2, most neurons have small spatio-temporal receptive fields responding selectively to oriented luminance contours (first order),...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154761/ https://www.ncbi.nlm.nih.gov/pubmed/25188576 http://dx.doi.org/10.1371/journal.pone.0106753 |
_version_ | 1782333472637976576 |
---|---|
author | An, Xu Gong, Hongliang Yin, Jiapeng Wang, Xiaochun Pan, Yanxia Zhang, Xian Lu, Yiliang Yang, Yupeng Toth, Zoltan Schiessl, Ingo McLoughlin, Niall Wang, Wei |
author_facet | An, Xu Gong, Hongliang Yin, Jiapeng Wang, Xiaochun Pan, Yanxia Zhang, Xian Lu, Yiliang Yang, Yupeng Toth, Zoltan Schiessl, Ingo McLoughlin, Niall Wang, Wei |
author_sort | An, Xu |
collection | PubMed |
description | Visual scenes can be readily decomposed into a variety of oriented components, the processing of which is vital for object segregation and recognition. In primate V1 and V2, most neurons have small spatio-temporal receptive fields responding selectively to oriented luminance contours (first order), while only a subgroup of neurons signal non-luminance defined contours (second order). So how is the orientation of second-order contours represented at the population level in macaque V1 and V2? Here we compared the population responses in macaque V1 and V2 to two types of second-order contour stimuli generated either by modulation of contrast or phase reversal with those to first-order contour stimuli. Using intrinsic signal optical imaging, we found that the orientation of second-order contour stimuli was represented invariantly in the orientation columns of both macaque V1 and V2. A physiologically constrained spatio-temporal energy model of V1 and V2 neuronal populations could reproduce all the recorded population responses. These findings suggest that, at the population level, the primate early visual system processes the orientation of second-order contours initially through a linear spatio-temporal filter mechanism. Our results of population responses to different second-order contour stimuli support the idea that the orientation maps in primate V1 and V2 can be described as a spatial-temporal energy map. |
format | Online Article Text |
id | pubmed-4154761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41547612014-09-08 Orientation-Cue Invariant Population Responses to Contrast-Modulated and Phase-Reversed Contour Stimuli in Macaque V1 and V2 An, Xu Gong, Hongliang Yin, Jiapeng Wang, Xiaochun Pan, Yanxia Zhang, Xian Lu, Yiliang Yang, Yupeng Toth, Zoltan Schiessl, Ingo McLoughlin, Niall Wang, Wei PLoS One Research Article Visual scenes can be readily decomposed into a variety of oriented components, the processing of which is vital for object segregation and recognition. In primate V1 and V2, most neurons have small spatio-temporal receptive fields responding selectively to oriented luminance contours (first order), while only a subgroup of neurons signal non-luminance defined contours (second order). So how is the orientation of second-order contours represented at the population level in macaque V1 and V2? Here we compared the population responses in macaque V1 and V2 to two types of second-order contour stimuli generated either by modulation of contrast or phase reversal with those to first-order contour stimuli. Using intrinsic signal optical imaging, we found that the orientation of second-order contour stimuli was represented invariantly in the orientation columns of both macaque V1 and V2. A physiologically constrained spatio-temporal energy model of V1 and V2 neuronal populations could reproduce all the recorded population responses. These findings suggest that, at the population level, the primate early visual system processes the orientation of second-order contours initially through a linear spatio-temporal filter mechanism. Our results of population responses to different second-order contour stimuli support the idea that the orientation maps in primate V1 and V2 can be described as a spatial-temporal energy map. Public Library of Science 2014-09-04 /pmc/articles/PMC4154761/ /pubmed/25188576 http://dx.doi.org/10.1371/journal.pone.0106753 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article An, Xu Gong, Hongliang Yin, Jiapeng Wang, Xiaochun Pan, Yanxia Zhang, Xian Lu, Yiliang Yang, Yupeng Toth, Zoltan Schiessl, Ingo McLoughlin, Niall Wang, Wei Orientation-Cue Invariant Population Responses to Contrast-Modulated and Phase-Reversed Contour Stimuli in Macaque V1 and V2 |
title | Orientation-Cue Invariant Population Responses to Contrast-Modulated and Phase-Reversed Contour Stimuli in Macaque V1 and V2 |
title_full | Orientation-Cue Invariant Population Responses to Contrast-Modulated and Phase-Reversed Contour Stimuli in Macaque V1 and V2 |
title_fullStr | Orientation-Cue Invariant Population Responses to Contrast-Modulated and Phase-Reversed Contour Stimuli in Macaque V1 and V2 |
title_full_unstemmed | Orientation-Cue Invariant Population Responses to Contrast-Modulated and Phase-Reversed Contour Stimuli in Macaque V1 and V2 |
title_short | Orientation-Cue Invariant Population Responses to Contrast-Modulated and Phase-Reversed Contour Stimuli in Macaque V1 and V2 |
title_sort | orientation-cue invariant population responses to contrast-modulated and phase-reversed contour stimuli in macaque v1 and v2 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154761/ https://www.ncbi.nlm.nih.gov/pubmed/25188576 http://dx.doi.org/10.1371/journal.pone.0106753 |
work_keys_str_mv | AT anxu orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT gonghongliang orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT yinjiapeng orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT wangxiaochun orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT panyanxia orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT zhangxian orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT luyiliang orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT yangyupeng orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT tothzoltan orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT schiesslingo orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT mcloughlinniall orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 AT wangwei orientationcueinvariantpopulationresponsestocontrastmodulatedandphasereversedcontourstimuliinmacaquev1andv2 |