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Rapid Bidirectional Reorganization of Cortical Microcircuits

Mature neocortex adapts to altered sensory input by changing neural activity in cortical circuits. The underlying cellular mechanisms remain unclear. We used blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) to show reorganization in somatosensory cortex elicited by al...

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Autores principales: Albieri, Giorgia, Barnes, Samuel J., de Celis Alonso, Benito, Cheetham, Claire E.J., Edwards, Clarissa E., Lowe, Andrew S., Karunaratne, Harini, Dear, John P., Lee, Kalok C., Finnerty, Gerald T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537443/
https://www.ncbi.nlm.nih.gov/pubmed/24836895
http://dx.doi.org/10.1093/cercor/bhu098
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author Albieri, Giorgia
Barnes, Samuel J.
de Celis Alonso, Benito
Cheetham, Claire E.J.
Edwards, Clarissa E.
Lowe, Andrew S.
Karunaratne, Harini
Dear, John P.
Lee, Kalok C.
Finnerty, Gerald T.
author_facet Albieri, Giorgia
Barnes, Samuel J.
de Celis Alonso, Benito
Cheetham, Claire E.J.
Edwards, Clarissa E.
Lowe, Andrew S.
Karunaratne, Harini
Dear, John P.
Lee, Kalok C.
Finnerty, Gerald T.
author_sort Albieri, Giorgia
collection PubMed
description Mature neocortex adapts to altered sensory input by changing neural activity in cortical circuits. The underlying cellular mechanisms remain unclear. We used blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) to show reorganization in somatosensory cortex elicited by altered whisker sensory input. We found that there was rapid expansion followed by retraction of whisker cortical maps. The cellular basis for the reorganization in primary somatosensory cortex was investigated with paired electrophysiological recordings in the periphery of the expanded whisker representation. During map expansion, the chance of finding a monosynaptic connection between pairs of pyramidal neurons increased 3-fold. Despite the rapid increase in local excitatory connectivity, the average strength and synaptic dynamics did not change, which suggests that new excitatory connections rapidly acquire the properties of established excitatory connections. During map retraction, entire excitatory connections between pyramidal neurons were lost. In contrast, connectivity between pyramidal neurons and fast spiking interneurons was unchanged. Hence, the changes in local excitatory connectivity did not occur in all circuits involving pyramidal neurons. Our data show that pyramidal neurons are recruited to and eliminated from local excitatory networks over days. These findings suggest that the local excitatory connectome is dynamic in mature neocortex.
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spelling pubmed-45374432015-08-17 Rapid Bidirectional Reorganization of Cortical Microcircuits Albieri, Giorgia Barnes, Samuel J. de Celis Alonso, Benito Cheetham, Claire E.J. Edwards, Clarissa E. Lowe, Andrew S. Karunaratne, Harini Dear, John P. Lee, Kalok C. Finnerty, Gerald T. Cereb Cortex Articles Mature neocortex adapts to altered sensory input by changing neural activity in cortical circuits. The underlying cellular mechanisms remain unclear. We used blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) to show reorganization in somatosensory cortex elicited by altered whisker sensory input. We found that there was rapid expansion followed by retraction of whisker cortical maps. The cellular basis for the reorganization in primary somatosensory cortex was investigated with paired electrophysiological recordings in the periphery of the expanded whisker representation. During map expansion, the chance of finding a monosynaptic connection between pairs of pyramidal neurons increased 3-fold. Despite the rapid increase in local excitatory connectivity, the average strength and synaptic dynamics did not change, which suggests that new excitatory connections rapidly acquire the properties of established excitatory connections. During map retraction, entire excitatory connections between pyramidal neurons were lost. In contrast, connectivity between pyramidal neurons and fast spiking interneurons was unchanged. Hence, the changes in local excitatory connectivity did not occur in all circuits involving pyramidal neurons. Our data show that pyramidal neurons are recruited to and eliminated from local excitatory networks over days. These findings suggest that the local excitatory connectome is dynamic in mature neocortex. Oxford University Press 2015-09 2014-05-16 /pmc/articles/PMC4537443/ /pubmed/24836895 http://dx.doi.org/10.1093/cercor/bhu098 Text en © The Author 2014. Published by Oxford University Press http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Albieri, Giorgia
Barnes, Samuel J.
de Celis Alonso, Benito
Cheetham, Claire E.J.
Edwards, Clarissa E.
Lowe, Andrew S.
Karunaratne, Harini
Dear, John P.
Lee, Kalok C.
Finnerty, Gerald T.
Rapid Bidirectional Reorganization of Cortical Microcircuits
title Rapid Bidirectional Reorganization of Cortical Microcircuits
title_full Rapid Bidirectional Reorganization of Cortical Microcircuits
title_fullStr Rapid Bidirectional Reorganization of Cortical Microcircuits
title_full_unstemmed Rapid Bidirectional Reorganization of Cortical Microcircuits
title_short Rapid Bidirectional Reorganization of Cortical Microcircuits
title_sort rapid bidirectional reorganization of cortical microcircuits
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537443/
https://www.ncbi.nlm.nih.gov/pubmed/24836895
http://dx.doi.org/10.1093/cercor/bhu098
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