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Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry

Across species, the performance of vocal signals can be modulated by the social environment. Zebra finches, for example, adjust their song performance when singing to females (‘female-directed’ or FD song) compared to when singing in isolation (‘undirected’ or UD song). These changes are salient, as...

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Autores principales: Zengin-Toktas, Yildiz, Woolley, Sarah Cushing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325550/
https://www.ncbi.nlm.nih.gov/pubmed/28235074
http://dx.doi.org/10.1371/journal.pone.0172944
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author Zengin-Toktas, Yildiz
Woolley, Sarah Cushing
author_facet Zengin-Toktas, Yildiz
Woolley, Sarah Cushing
author_sort Zengin-Toktas, Yildiz
collection PubMed
description Across species, the performance of vocal signals can be modulated by the social environment. Zebra finches, for example, adjust their song performance when singing to females (‘female-directed’ or FD song) compared to when singing in isolation (‘undirected’ or UD song). These changes are salient, as females prefer the FD song over the UD song. Despite the importance of these performance changes, the neural mechanisms underlying this social modulation remain poorly understood. Previous work in finches has established that expression of the immediate early gene EGR1 is increased during singing and modulated by social context within the vocal control circuitry. Here, we examined whether particular neural subpopulations within those vocal control regions exhibit similar modulations of EGR1 expression. We compared EGR1 expression in neurons expressing parvalbumin (PV), a calcium buffer that modulates network plasticity and homeostasis, among males that performed FD song, males that produced UD song, or males that did not sing. We found that, overall, singing but not social context significantly affected EGR1 expression in PV neurons throughout the vocal control nuclei. We observed differences in EGR1 expression between two classes of PV interneurons in the basal ganglia nucleus Area X. Additionally, we found that singing altered the amount of PV expression in neurons in HVC and Area X and that distinct PV interneuron types in Area X exhibited different patterns of modulation by singing. These data indicate that throughout the vocal control circuitry the singing-related regulation of EGR1 expression in PV neurons may be less influenced by social context than in other neuron types and raise the possibility of cell-type specific differences in plasticity and calcium buffering.
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spelling pubmed-53255502017-03-09 Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry Zengin-Toktas, Yildiz Woolley, Sarah Cushing PLoS One Research Article Across species, the performance of vocal signals can be modulated by the social environment. Zebra finches, for example, adjust their song performance when singing to females (‘female-directed’ or FD song) compared to when singing in isolation (‘undirected’ or UD song). These changes are salient, as females prefer the FD song over the UD song. Despite the importance of these performance changes, the neural mechanisms underlying this social modulation remain poorly understood. Previous work in finches has established that expression of the immediate early gene EGR1 is increased during singing and modulated by social context within the vocal control circuitry. Here, we examined whether particular neural subpopulations within those vocal control regions exhibit similar modulations of EGR1 expression. We compared EGR1 expression in neurons expressing parvalbumin (PV), a calcium buffer that modulates network plasticity and homeostasis, among males that performed FD song, males that produced UD song, or males that did not sing. We found that, overall, singing but not social context significantly affected EGR1 expression in PV neurons throughout the vocal control nuclei. We observed differences in EGR1 expression between two classes of PV interneurons in the basal ganglia nucleus Area X. Additionally, we found that singing altered the amount of PV expression in neurons in HVC and Area X and that distinct PV interneuron types in Area X exhibited different patterns of modulation by singing. These data indicate that throughout the vocal control circuitry the singing-related regulation of EGR1 expression in PV neurons may be less influenced by social context than in other neuron types and raise the possibility of cell-type specific differences in plasticity and calcium buffering. Public Library of Science 2017-02-24 /pmc/articles/PMC5325550/ /pubmed/28235074 http://dx.doi.org/10.1371/journal.pone.0172944 Text en © 2017 Zengin-Toktas, Woolley 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
Zengin-Toktas, Yildiz
Woolley, Sarah Cushing
Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry
title Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry
title_full Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry
title_fullStr Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry
title_full_unstemmed Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry
title_short Singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry
title_sort singing modulates parvalbumin interneurons throughout songbird forebrain vocal control circuitry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325550/
https://www.ncbi.nlm.nih.gov/pubmed/28235074
http://dx.doi.org/10.1371/journal.pone.0172944
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