Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783581365809184768 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7486661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kimjinwoo spontaneousretinalwavescangeneratelongrangehorizontalconnectivityinvisualcortex AT songmin spontaneousretinalwavescangeneratelongrangehorizontalconnectivityinvisualcortex AT jangjaeson spontaneousretinalwavescangeneratelongrangehorizontalconnectivityinvisualcortex AT paiksebum spontaneousretinalwavescangeneratelongrangehorizontalconnectivityinvisualcortex |