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Spontaneous Retinal Waves Can Generate Long-Range Horizontal Connectivity in Visual Cortex

In the primary visual cortex (V1) of higher mammals, long-range horizontal connections (LHCs) are observed to develop, linking iso-orientation domains of cortical tuning. It is unknown how this feature-specific wiring of circuitry develops before eye-opening. Here, we suggest that LHCs in V1 may ori...

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Autores principales: Kim, Jinwoo, Song, Min, Jang, Jaeson, Paik, Se-Bum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486661/
https://www.ncbi.nlm.nih.gov/pubmed/32680939
http://dx.doi.org/10.1523/JNEUROSCI.0649-20.2020
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author Kim, Jinwoo
Song, Min
Jang, Jaeson
Paik, Se-Bum
author_facet Kim, Jinwoo
Song, Min
Jang, Jaeson
Paik, Se-Bum
author_sort Kim, Jinwoo
collection PubMed
description In the primary visual cortex (V1) of higher mammals, long-range horizontal connections (LHCs) are observed to develop, linking iso-orientation domains of cortical tuning. It is unknown how this feature-specific wiring of circuitry develops before eye-opening. Here, we suggest that LHCs in V1 may originate from spatiotemporally structured feedforward activities generated from spontaneous retinal waves. Using model simulations based on the anatomy and observed activity patterns of the retina, we show that waves propagating in retinal mosaics can initialize the wiring of LHCs by coactivating neurons of similar tuning, whereas equivalent random activities cannot induce such organizations. Simulations showed that emerged LHCs can produce the patterned activities observed in V1, matching the topography of the underlying orientation map. The model can also reproduce feature-specific microcircuits in the salt-and-pepper organizations found in rodents. Our results imply that early peripheral activities contribute significantly to cortical development of functional circuits. SIGNIFICANCE STATEMENT Long-range horizontal connections (LHCs) in the primary visual cortex (V1) are observed to emerge before the onset of visual experience, thereby selectively connecting iso-domains of orientation map. However, it is unknown how such feature-specific wirings develop before eye-opening. Here, we show that LHCs in V1 may originate from the feature-specific activation of cortical neurons by spontaneous retinal waves during early developmental stages. Our simulations of a visual cortex model show that feedforward activities from the retina initialize the spatial organization of activity patterns in V1, which induces visual feature-specific wirings in the V1 neurons. Our model also explains the origin of cortical microcircuits observed in rodents, suggesting that the proposed developmental mechanism is universally applicable to circuits of various mammalian species.
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spelling pubmed-74866612021-08-19 Spontaneous Retinal Waves Can Generate Long-Range Horizontal Connectivity in Visual Cortex Kim, Jinwoo Song, Min Jang, Jaeson Paik, Se-Bum J Neurosci Research Articles In the primary visual cortex (V1) of higher mammals, long-range horizontal connections (LHCs) are observed to develop, linking iso-orientation domains of cortical tuning. It is unknown how this feature-specific wiring of circuitry develops before eye-opening. Here, we suggest that LHCs in V1 may originate from spatiotemporally structured feedforward activities generated from spontaneous retinal waves. Using model simulations based on the anatomy and observed activity patterns of the retina, we show that waves propagating in retinal mosaics can initialize the wiring of LHCs by coactivating neurons of similar tuning, whereas equivalent random activities cannot induce such organizations. Simulations showed that emerged LHCs can produce the patterned activities observed in V1, matching the topography of the underlying orientation map. The model can also reproduce feature-specific microcircuits in the salt-and-pepper organizations found in rodents. Our results imply that early peripheral activities contribute significantly to cortical development of functional circuits. SIGNIFICANCE STATEMENT Long-range horizontal connections (LHCs) in the primary visual cortex (V1) are observed to emerge before the onset of visual experience, thereby selectively connecting iso-domains of orientation map. However, it is unknown how such feature-specific wirings develop before eye-opening. Here, we show that LHCs in V1 may originate from the feature-specific activation of cortical neurons by spontaneous retinal waves during early developmental stages. Our simulations of a visual cortex model show that feedforward activities from the retina initialize the spatial organization of activity patterns in V1, which induces visual feature-specific wirings in the V1 neurons. Our model also explains the origin of cortical microcircuits observed in rodents, suggesting that the proposed developmental mechanism is universally applicable to circuits of various mammalian species. Society for Neuroscience 2020-08-19 /pmc/articles/PMC7486661/ /pubmed/32680939 http://dx.doi.org/10.1523/JNEUROSCI.0649-20.2020 Text en Copyright © 2020 Kim, Song et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License Creative Commons Attribution 4.0 International (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Kim, Jinwoo
Song, Min
Jang, Jaeson
Paik, Se-Bum
Spontaneous Retinal Waves Can Generate Long-Range Horizontal Connectivity in Visual Cortex
title Spontaneous Retinal Waves Can Generate Long-Range Horizontal Connectivity in Visual Cortex
title_full Spontaneous Retinal Waves Can Generate Long-Range Horizontal Connectivity in Visual Cortex
title_fullStr Spontaneous Retinal Waves Can Generate Long-Range Horizontal Connectivity in Visual Cortex
title_full_unstemmed Spontaneous Retinal Waves Can Generate Long-Range Horizontal Connectivity in Visual Cortex
title_short Spontaneous Retinal Waves Can Generate Long-Range Horizontal Connectivity in Visual Cortex
title_sort spontaneous retinal waves can generate long-range horizontal connectivity in visual cortex
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486661/
https://www.ncbi.nlm.nih.gov/pubmed/32680939
http://dx.doi.org/10.1523/JNEUROSCI.0649-20.2020
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