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Distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque V1 microcircuits
Complex scene perception depends upon the interaction between signals from the classical receptive field (CRF) and the extra-classical receptive field (eCRF) in primary visual cortex (V1) neurons. Although much is known about V1 eCRF properties, we do not yet know how the underlying mechanisms map o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253173/ https://www.ncbi.nlm.nih.gov/pubmed/32458798 http://dx.doi.org/10.7554/eLife.54264 |
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author | Henry, Christopher A Jazayeri, Mehrdad Shapley, Robert M Hawken, Michael J |
author_facet | Henry, Christopher A Jazayeri, Mehrdad Shapley, Robert M Hawken, Michael J |
author_sort | Henry, Christopher A |
collection | PubMed |
description | Complex scene perception depends upon the interaction between signals from the classical receptive field (CRF) and the extra-classical receptive field (eCRF) in primary visual cortex (V1) neurons. Although much is known about V1 eCRF properties, we do not yet know how the underlying mechanisms map onto the cortical microcircuit. We probed the spatio-temporal dynamics of eCRF modulation using a reverse correlation paradigm, and found three principal eCRF mechanisms: tuned-facilitation, untuned-suppression, and tuned-suppression. Each mechanism had a distinct timing and spatial profile. Laminar analysis showed that the timing, orientation-tuning, and strength of eCRF mechanisms had distinct signatures within magnocellular and parvocellular processing streams in the V1 microcircuit. The existence of multiple eCRF mechanisms provides new insights into how V1 responds to spatial context. Modeling revealed that the differences in timing and scale of these mechanisms predicted distinct patterns of net modulation, reconciling many previous disparate physiological and psychophysical findings. |
format | Online Article Text |
id | pubmed-7253173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-72531732020-05-28 Distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque V1 microcircuits Henry, Christopher A Jazayeri, Mehrdad Shapley, Robert M Hawken, Michael J eLife Neuroscience Complex scene perception depends upon the interaction between signals from the classical receptive field (CRF) and the extra-classical receptive field (eCRF) in primary visual cortex (V1) neurons. Although much is known about V1 eCRF properties, we do not yet know how the underlying mechanisms map onto the cortical microcircuit. We probed the spatio-temporal dynamics of eCRF modulation using a reverse correlation paradigm, and found three principal eCRF mechanisms: tuned-facilitation, untuned-suppression, and tuned-suppression. Each mechanism had a distinct timing and spatial profile. Laminar analysis showed that the timing, orientation-tuning, and strength of eCRF mechanisms had distinct signatures within magnocellular and parvocellular processing streams in the V1 microcircuit. The existence of multiple eCRF mechanisms provides new insights into how V1 responds to spatial context. Modeling revealed that the differences in timing and scale of these mechanisms predicted distinct patterns of net modulation, reconciling many previous disparate physiological and psychophysical findings. eLife Sciences Publications, Ltd 2020-05-27 /pmc/articles/PMC7253173/ /pubmed/32458798 http://dx.doi.org/10.7554/eLife.54264 Text en © 2020, Henry et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Henry, Christopher A Jazayeri, Mehrdad Shapley, Robert M Hawken, Michael J Distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque V1 microcircuits |
title | Distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque V1 microcircuits |
title_full | Distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque V1 microcircuits |
title_fullStr | Distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque V1 microcircuits |
title_full_unstemmed | Distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque V1 microcircuits |
title_short | Distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque V1 microcircuits |
title_sort | distinct spatiotemporal mechanisms underlie extra-classical receptive field modulation in macaque v1 microcircuits |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253173/ https://www.ncbi.nlm.nih.gov/pubmed/32458798 http://dx.doi.org/10.7554/eLife.54264 |
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