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Spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex
Neuronal responses and topographic organization of feature selectivity in the cerebral cortex are shaped by ascending inputs and by intracortical connectivity. The mammalian primary auditory cortex has a tonotopic arrangement at large spatial scales (greater than 300 microns). This large-scale archi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949116/ https://www.ncbi.nlm.nih.gov/pubmed/24653677 http://dx.doi.org/10.3389/fncir.2014.00015 |
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author | Watkins, Paul V. Kao, Joseph P. Y. Kanold, Patrick O. |
author_facet | Watkins, Paul V. Kao, Joseph P. Y. Kanold, Patrick O. |
author_sort | Watkins, Paul V. |
collection | PubMed |
description | Neuronal responses and topographic organization of feature selectivity in the cerebral cortex are shaped by ascending inputs and by intracortical connectivity. The mammalian primary auditory cortex has a tonotopic arrangement at large spatial scales (greater than 300 microns). This large-scale architecture breaks down in supragranular layers at smaller scales (around 300 microns), where nearby frequency and sound level tuning properties can be quite heterogeneous. Since layer 4 has a more homogeneous architecture, the heterogeneity in supragranular layers might be caused by heterogeneous ascending input or via heterogeneous intralaminar connections. Here we measure the functional 2-dimensional spatial connectivity pattern of the supragranular auditory cortex on micro-column scales. In general connection probability decreases with radial distance from each neuron, but the decrease is steeper in the isofrequency axis leading to an anisotropic distribution of connection probability with respect to the tonotopic axis. In addition to this radial decrease in connection probability we find a patchy organization of inhibitory and excitatory synaptic inputs that is also anisotropic with respect to the tonotopic axis. These periodicities are at spatial scales of ~100 and ~300 μm. While these spatial periodicities show anisotropy in auditory cortex, they are isotropic in visual cortex, indicating region specific differences in intralaminar connections. Together our results show that layer 2/3 neurons in auditory cortex show specific spatial intralaminar connectivity despite the overtly heterogeneous tuning properties. |
format | Online Article Text |
id | pubmed-3949116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39491162014-03-20 Spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex Watkins, Paul V. Kao, Joseph P. Y. Kanold, Patrick O. Front Neural Circuits Neuroscience Neuronal responses and topographic organization of feature selectivity in the cerebral cortex are shaped by ascending inputs and by intracortical connectivity. The mammalian primary auditory cortex has a tonotopic arrangement at large spatial scales (greater than 300 microns). This large-scale architecture breaks down in supragranular layers at smaller scales (around 300 microns), where nearby frequency and sound level tuning properties can be quite heterogeneous. Since layer 4 has a more homogeneous architecture, the heterogeneity in supragranular layers might be caused by heterogeneous ascending input or via heterogeneous intralaminar connections. Here we measure the functional 2-dimensional spatial connectivity pattern of the supragranular auditory cortex on micro-column scales. In general connection probability decreases with radial distance from each neuron, but the decrease is steeper in the isofrequency axis leading to an anisotropic distribution of connection probability with respect to the tonotopic axis. In addition to this radial decrease in connection probability we find a patchy organization of inhibitory and excitatory synaptic inputs that is also anisotropic with respect to the tonotopic axis. These periodicities are at spatial scales of ~100 and ~300 μm. While these spatial periodicities show anisotropy in auditory cortex, they are isotropic in visual cortex, indicating region specific differences in intralaminar connections. Together our results show that layer 2/3 neurons in auditory cortex show specific spatial intralaminar connectivity despite the overtly heterogeneous tuning properties. Frontiers Media S.A. 2014-03-11 /pmc/articles/PMC3949116/ /pubmed/24653677 http://dx.doi.org/10.3389/fncir.2014.00015 Text en Copyright © 2014 Watkins, Kao and Kanold. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Watkins, Paul V. Kao, Joseph P. Y. Kanold, Patrick O. Spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex |
title | Spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex |
title_full | Spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex |
title_fullStr | Spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex |
title_full_unstemmed | Spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex |
title_short | Spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex |
title_sort | spatial pattern of intra-laminar connectivity in supragranular mouse auditory cortex |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949116/ https://www.ncbi.nlm.nih.gov/pubmed/24653677 http://dx.doi.org/10.3389/fncir.2014.00015 |
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