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Transient callosal projections of L4 neurons are eliminated for the acquisition of local connectivity
Interhemispheric axons of the corpus callosum (CC) facilitate the higher order functions of the cerebral cortex. According to current views, callosal and non-callosal fates are determined early after a neuron’s birth, and certain populations, such as cortical layer (L) 4 excitatory neurons of the pr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779895/ https://www.ncbi.nlm.nih.gov/pubmed/31591398 http://dx.doi.org/10.1038/s41467-019-12495-w |
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author | De León Reyes, N. S. Mederos, S. Varela, I. Weiss, L. A. Perea, G. Galazo, M. J. Nieto, M. |
author_facet | De León Reyes, N. S. Mederos, S. Varela, I. Weiss, L. A. Perea, G. Galazo, M. J. Nieto, M. |
author_sort | De León Reyes, N. S. |
collection | PubMed |
description | Interhemispheric axons of the corpus callosum (CC) facilitate the higher order functions of the cerebral cortex. According to current views, callosal and non-callosal fates are determined early after a neuron’s birth, and certain populations, such as cortical layer (L) 4 excitatory neurons of the primary somatosensory (S1) barrel, project only ipsilaterally. Using a novel axonal-retrotracing strategy and GFP-targeted visualization of Rorb(+) neurons, we instead demonstrate that L4 neurons develop transient interhemispheric axons. Locally restricted L4 connectivity emerges when exuberant contralateral axons are refined in an area- and layer-specific manner during postnatal development. Surgical and genetic interventions of sensory circuits demonstrate that refinement rates depend on distinct inputs from sensory-specific thalamic nuclei. Reductions in input-dependent refinement result in mature functional interhemispheric hyperconnectivity, demonstrating the plasticity and bona fide callosal potential of L4 neurons. Thus, L4 neurons discard alternative interhemispheric circuits as instructed by thalamic input. This may ensure optimal wiring. |
format | Online Article Text |
id | pubmed-6779895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67798952019-10-09 Transient callosal projections of L4 neurons are eliminated for the acquisition of local connectivity De León Reyes, N. S. Mederos, S. Varela, I. Weiss, L. A. Perea, G. Galazo, M. J. Nieto, M. Nat Commun Article Interhemispheric axons of the corpus callosum (CC) facilitate the higher order functions of the cerebral cortex. According to current views, callosal and non-callosal fates are determined early after a neuron’s birth, and certain populations, such as cortical layer (L) 4 excitatory neurons of the primary somatosensory (S1) barrel, project only ipsilaterally. Using a novel axonal-retrotracing strategy and GFP-targeted visualization of Rorb(+) neurons, we instead demonstrate that L4 neurons develop transient interhemispheric axons. Locally restricted L4 connectivity emerges when exuberant contralateral axons are refined in an area- and layer-specific manner during postnatal development. Surgical and genetic interventions of sensory circuits demonstrate that refinement rates depend on distinct inputs from sensory-specific thalamic nuclei. Reductions in input-dependent refinement result in mature functional interhemispheric hyperconnectivity, demonstrating the plasticity and bona fide callosal potential of L4 neurons. Thus, L4 neurons discard alternative interhemispheric circuits as instructed by thalamic input. This may ensure optimal wiring. Nature Publishing Group UK 2019-10-07 /pmc/articles/PMC6779895/ /pubmed/31591398 http://dx.doi.org/10.1038/s41467-019-12495-w Text en © The Author(s) 2019 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 De León Reyes, N. S. Mederos, S. Varela, I. Weiss, L. A. Perea, G. Galazo, M. J. Nieto, M. Transient callosal projections of L4 neurons are eliminated for the acquisition of local connectivity |
title | Transient callosal projections of L4 neurons are eliminated for the acquisition of local connectivity |
title_full | Transient callosal projections of L4 neurons are eliminated for the acquisition of local connectivity |
title_fullStr | Transient callosal projections of L4 neurons are eliminated for the acquisition of local connectivity |
title_full_unstemmed | Transient callosal projections of L4 neurons are eliminated for the acquisition of local connectivity |
title_short | Transient callosal projections of L4 neurons are eliminated for the acquisition of local connectivity |
title_sort | transient callosal projections of l4 neurons are eliminated for the acquisition of local connectivity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779895/ https://www.ncbi.nlm.nih.gov/pubmed/31591398 http://dx.doi.org/10.1038/s41467-019-12495-w |
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