Cargando…

Learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination

From observations in rodents, it has been suggested that the cellular basis of learning-dependent changes, detected using structural MRI, may be increased dendritic spine density, alterations in astrocyte volume, and adaptations within intracortical myelin. Myelin plasticity is crucial for neurologi...

Descripción completa

Detalles Bibliográficos
Autores principales: Mediavilla, Tomas, Özalay, Özgün, Estévez-Silva, Héctor M, Frias, Bárbara, Orädd, Greger, Sultan, Fahad R, Brozzoli, Claudio, Garzón, Benjamín, Lövdén, Martin, Marcellino, Daniel J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678357/
https://www.ncbi.nlm.nih.gov/pubmed/36350292
http://dx.doi.org/10.7554/eLife.77432
_version_ 1784833973143207936
author Mediavilla, Tomas
Özalay, Özgün
Estévez-Silva, Héctor M
Frias, Bárbara
Orädd, Greger
Sultan, Fahad R
Brozzoli, Claudio
Garzón, Benjamín
Lövdén, Martin
Marcellino, Daniel J
author_facet Mediavilla, Tomas
Özalay, Özgün
Estévez-Silva, Héctor M
Frias, Bárbara
Orädd, Greger
Sultan, Fahad R
Brozzoli, Claudio
Garzón, Benjamín
Lövdén, Martin
Marcellino, Daniel J
author_sort Mediavilla, Tomas
collection PubMed
description From observations in rodents, it has been suggested that the cellular basis of learning-dependent changes, detected using structural MRI, may be increased dendritic spine density, alterations in astrocyte volume, and adaptations within intracortical myelin. Myelin plasticity is crucial for neurological function, and active myelination is required for learning and memory. However, the dynamics of myelin plasticity and how it relates to morphometric-based measurements of structural plasticity remains unknown. We used a motor skill learning paradigm in male mice to evaluate experience-dependent brain plasticity by voxel-based morphometry (VBM) in longitudinal MRI, combined with a cross-sectional immunohistochemical investigation. Whole-brain VBM revealed nonlinear decreases in gray matter volume (GMV) juxtaposed to nonlinear increases in white matter volume (WMV) within GM that were best modeled by an asymptotic time course. Using an atlas-based cortical mask, we found nonlinear changes with learning in primary and secondary motor areas and in somatosensory cortex. Analysis of cross-sectional myelin immunoreactivity in forelimb somatosensory cortex confirmed an increase in myelin immunoreactivity followed by a return towards baseline levels. Further investigations using quantitative confocal microscopy confirmed these changes specifically to the length density of myelinated axons. The absence of significant histological changes in cortical thickness suggests that nonlinear morphometric changes are likely due to changes in intracortical myelin for which morphometric WMV in somatosensory cortex significantly correlated with myelin immunoreactivity. Together, these observations indicate a nonlinear increase of intracortical myelin during learning and support the hypothesis that myelin is a component of structural changes observed by VBM during learning.
format Online
Article
Text
id pubmed-9678357
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-96783572022-11-22 Learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination Mediavilla, Tomas Özalay, Özgün Estévez-Silva, Héctor M Frias, Bárbara Orädd, Greger Sultan, Fahad R Brozzoli, Claudio Garzón, Benjamín Lövdén, Martin Marcellino, Daniel J eLife Neuroscience From observations in rodents, it has been suggested that the cellular basis of learning-dependent changes, detected using structural MRI, may be increased dendritic spine density, alterations in astrocyte volume, and adaptations within intracortical myelin. Myelin plasticity is crucial for neurological function, and active myelination is required for learning and memory. However, the dynamics of myelin plasticity and how it relates to morphometric-based measurements of structural plasticity remains unknown. We used a motor skill learning paradigm in male mice to evaluate experience-dependent brain plasticity by voxel-based morphometry (VBM) in longitudinal MRI, combined with a cross-sectional immunohistochemical investigation. Whole-brain VBM revealed nonlinear decreases in gray matter volume (GMV) juxtaposed to nonlinear increases in white matter volume (WMV) within GM that were best modeled by an asymptotic time course. Using an atlas-based cortical mask, we found nonlinear changes with learning in primary and secondary motor areas and in somatosensory cortex. Analysis of cross-sectional myelin immunoreactivity in forelimb somatosensory cortex confirmed an increase in myelin immunoreactivity followed by a return towards baseline levels. Further investigations using quantitative confocal microscopy confirmed these changes specifically to the length density of myelinated axons. The absence of significant histological changes in cortical thickness suggests that nonlinear morphometric changes are likely due to changes in intracortical myelin for which morphometric WMV in somatosensory cortex significantly correlated with myelin immunoreactivity. Together, these observations indicate a nonlinear increase of intracortical myelin during learning and support the hypothesis that myelin is a component of structural changes observed by VBM during learning. eLife Sciences Publications, Ltd 2022-11-09 /pmc/articles/PMC9678357/ /pubmed/36350292 http://dx.doi.org/10.7554/eLife.77432 Text en © 2022, Mediavilla et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Mediavilla, Tomas
Özalay, Özgün
Estévez-Silva, Héctor M
Frias, Bárbara
Orädd, Greger
Sultan, Fahad R
Brozzoli, Claudio
Garzón, Benjamín
Lövdén, Martin
Marcellino, Daniel J
Learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination
title Learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination
title_full Learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination
title_fullStr Learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination
title_full_unstemmed Learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination
title_short Learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination
title_sort learning-related contraction of gray matter in rodent sensorimotor cortex is associated with adaptive myelination
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678357/
https://www.ncbi.nlm.nih.gov/pubmed/36350292
http://dx.doi.org/10.7554/eLife.77432
work_keys_str_mv AT mediavillatomas learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT ozalayozgun learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT estevezsilvahectorm learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT friasbarbara learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT oraddgreger learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT sultanfahadr learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT brozzoliclaudio learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT garzonbenjamin learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT lovdenmartin learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination
AT marcellinodanielj learningrelatedcontractionofgraymatterinrodentsensorimotorcortexisassociatedwithadaptivemyelination