Cargando…

Evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the Ca(2+) binding protein S100β

The medial prefrontal cortex (mPFC) is important for cognitive flexibility, the ability to switch between two task-relevant dimensions. Changes in neuronal oscillations and alterations in the coupling across frequency ranges have been correlated with attention and cognitive flexibility. Here we show...

Descripción completa

Detalles Bibliográficos
Autores principales: Brockett, Adam T., Kane, Gary A., Monari, Patrick K., Briones, Brandy A., Vigneron, Pierre-Antoine, Barber, Gabriela A., Bermudez, Andres, Dieffenbach, Uma, Kloth, Alexander D., Buschman, Timothy J., Gould, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903631/
https://www.ncbi.nlm.nih.gov/pubmed/29664924
http://dx.doi.org/10.1371/journal.pone.0195726
_version_ 1783314964466892800
author Brockett, Adam T.
Kane, Gary A.
Monari, Patrick K.
Briones, Brandy A.
Vigneron, Pierre-Antoine
Barber, Gabriela A.
Bermudez, Andres
Dieffenbach, Uma
Kloth, Alexander D.
Buschman, Timothy J.
Gould, Elizabeth
author_facet Brockett, Adam T.
Kane, Gary A.
Monari, Patrick K.
Briones, Brandy A.
Vigneron, Pierre-Antoine
Barber, Gabriela A.
Bermudez, Andres
Dieffenbach, Uma
Kloth, Alexander D.
Buschman, Timothy J.
Gould, Elizabeth
author_sort Brockett, Adam T.
collection PubMed
description The medial prefrontal cortex (mPFC) is important for cognitive flexibility, the ability to switch between two task-relevant dimensions. Changes in neuronal oscillations and alterations in the coupling across frequency ranges have been correlated with attention and cognitive flexibility. Here we show that astrocytes in the mPFC of adult male Sprague Dawley rats, participate in cognitive flexibility through the astrocyte-specific Ca(2+) binding protein S100β, which improves cognitive flexibility and increases phase amplitude coupling between theta and gamma oscillations. We further show that reduction of astrocyte number in the mPFC impairs cognitive flexibility and diminishes delta, alpha and gamma power. Conversely, chemogenetic activation of astrocytic intracellular Ca(2+) signaling in the mPFC enhances cognitive flexibility, while inactivation of endogenous S100β among chemogenetically activated astrocytes in the mPFC prevents this improvement. Collectively, our work suggests that astrocytes make important contributions to cognitive flexibility and that they do so by releasing a Ca(2+) binding protein which in turn enhances coordinated neuronal oscillations.
format Online
Article
Text
id pubmed-5903631
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-59036312018-04-27 Evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the Ca(2+) binding protein S100β Brockett, Adam T. Kane, Gary A. Monari, Patrick K. Briones, Brandy A. Vigneron, Pierre-Antoine Barber, Gabriela A. Bermudez, Andres Dieffenbach, Uma Kloth, Alexander D. Buschman, Timothy J. Gould, Elizabeth PLoS One Research Article The medial prefrontal cortex (mPFC) is important for cognitive flexibility, the ability to switch between two task-relevant dimensions. Changes in neuronal oscillations and alterations in the coupling across frequency ranges have been correlated with attention and cognitive flexibility. Here we show that astrocytes in the mPFC of adult male Sprague Dawley rats, participate in cognitive flexibility through the astrocyte-specific Ca(2+) binding protein S100β, which improves cognitive flexibility and increases phase amplitude coupling between theta and gamma oscillations. We further show that reduction of astrocyte number in the mPFC impairs cognitive flexibility and diminishes delta, alpha and gamma power. Conversely, chemogenetic activation of astrocytic intracellular Ca(2+) signaling in the mPFC enhances cognitive flexibility, while inactivation of endogenous S100β among chemogenetically activated astrocytes in the mPFC prevents this improvement. Collectively, our work suggests that astrocytes make important contributions to cognitive flexibility and that they do so by releasing a Ca(2+) binding protein which in turn enhances coordinated neuronal oscillations. Public Library of Science 2018-04-17 /pmc/articles/PMC5903631/ /pubmed/29664924 http://dx.doi.org/10.1371/journal.pone.0195726 Text en © 2018 Brockett et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Brockett, Adam T.
Kane, Gary A.
Monari, Patrick K.
Briones, Brandy A.
Vigneron, Pierre-Antoine
Barber, Gabriela A.
Bermudez, Andres
Dieffenbach, Uma
Kloth, Alexander D.
Buschman, Timothy J.
Gould, Elizabeth
Evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the Ca(2+) binding protein S100β
title Evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the Ca(2+) binding protein S100β
title_full Evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the Ca(2+) binding protein S100β
title_fullStr Evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the Ca(2+) binding protein S100β
title_full_unstemmed Evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the Ca(2+) binding protein S100β
title_short Evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the Ca(2+) binding protein S100β
title_sort evidence supporting a role for astrocytes in the regulation of cognitive flexibility and neuronal oscillations through the ca(2+) binding protein s100β
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903631/
https://www.ncbi.nlm.nih.gov/pubmed/29664924
http://dx.doi.org/10.1371/journal.pone.0195726
work_keys_str_mv AT brockettadamt evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT kanegarya evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT monaripatrickk evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT brionesbrandya evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT vigneronpierreantoine evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT barbergabrielaa evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT bermudezandres evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT dieffenbachuma evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT klothalexanderd evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT buschmantimothyj evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b
AT gouldelizabeth evidencesupportingaroleforastrocytesintheregulationofcognitiveflexibilityandneuronaloscillationsthroughtheca2bindingproteins100b