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Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons

The integration of synaptic inputs onto dendrites provides the basis for neuronal computation. Whereas recent studies have begun to outline the spatial organization of synaptic inputs on individual neurons, the underlying principles related to the specific neural functions are not well understood. H...

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Autores principales: Ju, Niansheng, Li, Yang, Liu, Fang, Jiang, Hongfei, Macknik, Stephen L., Martinez-Conde, Susana, Tang, Shiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000673/
https://www.ncbi.nlm.nih.gov/pubmed/32019929
http://dx.doi.org/10.1038/s41467-020-14501-y
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author Ju, Niansheng
Li, Yang
Liu, Fang
Jiang, Hongfei
Macknik, Stephen L.
Martinez-Conde, Susana
Tang, Shiming
author_facet Ju, Niansheng
Li, Yang
Liu, Fang
Jiang, Hongfei
Macknik, Stephen L.
Martinez-Conde, Susana
Tang, Shiming
author_sort Ju, Niansheng
collection PubMed
description The integration of synaptic inputs onto dendrites provides the basis for neuronal computation. Whereas recent studies have begun to outline the spatial organization of synaptic inputs on individual neurons, the underlying principles related to the specific neural functions are not well understood. Here we perform two-photon dendritic imaging with a genetically-encoded glutamate sensor in awake monkeys, and map the excitatory synaptic inputs on dendrites of individual V1 superficial layer neurons with high spatial and temporal resolution. We find a functional integration and trade-off between orientation-selective and color-selective inputs in basal dendrites of individual V1 neurons. Synaptic inputs on dendrites are spatially clustered by stimulus feature, but functionally scattered in multidimensional feature space, providing a potential substrate of local feature integration on dendritic branches. Furthermore, apical dendrite inputs have larger receptive fields and longer response latencies than basal dendrite inputs, suggesting a dominant role for apical dendrites in integrating feedback in visual information processing.
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spelling pubmed-70006732020-02-06 Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons Ju, Niansheng Li, Yang Liu, Fang Jiang, Hongfei Macknik, Stephen L. Martinez-Conde, Susana Tang, Shiming Nat Commun Article The integration of synaptic inputs onto dendrites provides the basis for neuronal computation. Whereas recent studies have begun to outline the spatial organization of synaptic inputs on individual neurons, the underlying principles related to the specific neural functions are not well understood. Here we perform two-photon dendritic imaging with a genetically-encoded glutamate sensor in awake monkeys, and map the excitatory synaptic inputs on dendrites of individual V1 superficial layer neurons with high spatial and temporal resolution. We find a functional integration and trade-off between orientation-selective and color-selective inputs in basal dendrites of individual V1 neurons. Synaptic inputs on dendrites are spatially clustered by stimulus feature, but functionally scattered in multidimensional feature space, providing a potential substrate of local feature integration on dendritic branches. Furthermore, apical dendrite inputs have larger receptive fields and longer response latencies than basal dendrite inputs, suggesting a dominant role for apical dendrites in integrating feedback in visual information processing. Nature Publishing Group UK 2020-02-04 /pmc/articles/PMC7000673/ /pubmed/32019929 http://dx.doi.org/10.1038/s41467-020-14501-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ju, Niansheng
Li, Yang
Liu, Fang
Jiang, Hongfei
Macknik, Stephen L.
Martinez-Conde, Susana
Tang, Shiming
Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons
title Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons
title_full Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons
title_fullStr Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons
title_full_unstemmed Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons
title_short Spatiotemporal functional organization of excitatory synaptic inputs onto macaque V1 neurons
title_sort spatiotemporal functional organization of excitatory synaptic inputs onto macaque v1 neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000673/
https://www.ncbi.nlm.nih.gov/pubmed/32019929
http://dx.doi.org/10.1038/s41467-020-14501-y
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