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The anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex
BACKGROUND: Alterations in the development of neuronal connectivity can result in dramatic outcomes for brain function. In the cerebral cortex, most sensorimotor and higher-order functions require coordination between precise regions of both hemispheres through the axons that form the corpus callosu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058258/ https://www.ncbi.nlm.nih.gov/pubmed/32166131 http://dx.doi.org/10.1177/2398212817694888 |
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author | Fenlon, Laura R. Suárez, Rodrigo Richards, Linda J. |
author_facet | Fenlon, Laura R. Suárez, Rodrigo Richards, Linda J. |
author_sort | Fenlon, Laura R. |
collection | PubMed |
description | BACKGROUND: Alterations in the development of neuronal connectivity can result in dramatic outcomes for brain function. In the cerebral cortex, most sensorimotor and higher-order functions require coordination between precise regions of both hemispheres through the axons that form the corpus callosum. However, little is known about how callosal axons locate and innervate their contralateral targets. METHODS: Here, we use a combination of in utero electroporation, retrograde tracing, sensory deprivation and high-resolution axonal quantification to investigate the development, organisation and activity dependence of callosal axons arising from the primary somatosensory cortex of mice. RESULTS: We show that distinct contralateral projections arise from different neuronal populations and form homotopic and heterotopic circuits. Callosal axons innervate the contralateral hemisphere following a dorsomedial to ventrolateral and region-specific order. Furthermore, we identify two periods of region- and layer-specific developmental exuberance that correspond to initial callosal axon innervation and subsequent arborisation. Early sensory deprivation affects only the latter of these events. CONCLUSION: Taken together, these results reveal the main developmental events of contralateral callosal targeting and may aid future understanding of the formation and pathologies of brain connectivity. |
format | Online Article Text |
id | pubmed-7058258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-70582582020-03-12 The anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex Fenlon, Laura R. Suárez, Rodrigo Richards, Linda J. Brain Neurosci Adv Research Paper BACKGROUND: Alterations in the development of neuronal connectivity can result in dramatic outcomes for brain function. In the cerebral cortex, most sensorimotor and higher-order functions require coordination between precise regions of both hemispheres through the axons that form the corpus callosum. However, little is known about how callosal axons locate and innervate their contralateral targets. METHODS: Here, we use a combination of in utero electroporation, retrograde tracing, sensory deprivation and high-resolution axonal quantification to investigate the development, organisation and activity dependence of callosal axons arising from the primary somatosensory cortex of mice. RESULTS: We show that distinct contralateral projections arise from different neuronal populations and form homotopic and heterotopic circuits. Callosal axons innervate the contralateral hemisphere following a dorsomedial to ventrolateral and region-specific order. Furthermore, we identify two periods of region- and layer-specific developmental exuberance that correspond to initial callosal axon innervation and subsequent arborisation. Early sensory deprivation affects only the latter of these events. CONCLUSION: Taken together, these results reveal the main developmental events of contralateral callosal targeting and may aid future understanding of the formation and pathologies of brain connectivity. SAGE Publications 2017-03-08 /pmc/articles/PMC7058258/ /pubmed/32166131 http://dx.doi.org/10.1177/2398212817694888 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Paper Fenlon, Laura R. Suárez, Rodrigo Richards, Linda J. The anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex |
title | The anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex |
title_full | The anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex |
title_fullStr | The anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex |
title_full_unstemmed | The anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex |
title_short | The anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex |
title_sort | anatomy, organisation and development of contralateral callosal projections of the mouse somatosensory cortex |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058258/ https://www.ncbi.nlm.nih.gov/pubmed/32166131 http://dx.doi.org/10.1177/2398212817694888 |
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