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The Spatiotemporal Organization of the Striatum Encodes Action Space

Activity in striatal direct- and indirect-pathway spiny projection neurons (SPNs) is critical for proper movement. However, little is known about the spatiotemporal organization of this activity. We investigated the spatiotemporal organization of SPN ensemble activity in mice during self-paced, natu...

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Detalles Bibliográficos
Autores principales: Klaus, Andreas, Martins, Gabriela J., Paixao, Vitor B., Zhou, Pengcheng, Paninski, Liam, Costa, Rui M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584673/
https://www.ncbi.nlm.nih.gov/pubmed/28858619
http://dx.doi.org/10.1016/j.neuron.2017.08.015
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author Klaus, Andreas
Martins, Gabriela J.
Paixao, Vitor B.
Zhou, Pengcheng
Paninski, Liam
Costa, Rui M.
author_facet Klaus, Andreas
Martins, Gabriela J.
Paixao, Vitor B.
Zhou, Pengcheng
Paninski, Liam
Costa, Rui M.
author_sort Klaus, Andreas
collection PubMed
description Activity in striatal direct- and indirect-pathway spiny projection neurons (SPNs) is critical for proper movement. However, little is known about the spatiotemporal organization of this activity. We investigated the spatiotemporal organization of SPN ensemble activity in mice during self-paced, natural movements using microendoscopic imaging. Activity in both pathways showed predominantly local but also some long-range correlations. Using a novel approach to cluster and quantify behaviors based on continuous accelerometer and video data, we found that SPN ensembles active during specific actions were spatially closer and more correlated overall. Furthermore, similarity between different actions corresponded to the similarity between SPN ensemble patterns, irrespective of movement speed. Consistently, the accuracy of decoding behavior from SPN ensemble patterns was directly related to the dissimilarity between behavioral clusters. These results identify a predominantly local, but not spatially compact, organization of direct- and indirect-pathway SPN activity that maps action space independently of movement speed.
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spelling pubmed-55846732017-09-14 The Spatiotemporal Organization of the Striatum Encodes Action Space Klaus, Andreas Martins, Gabriela J. Paixao, Vitor B. Zhou, Pengcheng Paninski, Liam Costa, Rui M. Neuron Article Activity in striatal direct- and indirect-pathway spiny projection neurons (SPNs) is critical for proper movement. However, little is known about the spatiotemporal organization of this activity. We investigated the spatiotemporal organization of SPN ensemble activity in mice during self-paced, natural movements using microendoscopic imaging. Activity in both pathways showed predominantly local but also some long-range correlations. Using a novel approach to cluster and quantify behaviors based on continuous accelerometer and video data, we found that SPN ensembles active during specific actions were spatially closer and more correlated overall. Furthermore, similarity between different actions corresponded to the similarity between SPN ensemble patterns, irrespective of movement speed. Consistently, the accuracy of decoding behavior from SPN ensemble patterns was directly related to the dissimilarity between behavioral clusters. These results identify a predominantly local, but not spatially compact, organization of direct- and indirect-pathway SPN activity that maps action space independently of movement speed. Cell Press 2017-08-30 /pmc/articles/PMC5584673/ /pubmed/28858619 http://dx.doi.org/10.1016/j.neuron.2017.08.015 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Klaus, Andreas
Martins, Gabriela J.
Paixao, Vitor B.
Zhou, Pengcheng
Paninski, Liam
Costa, Rui M.
The Spatiotemporal Organization of the Striatum Encodes Action Space
title The Spatiotemporal Organization of the Striatum Encodes Action Space
title_full The Spatiotemporal Organization of the Striatum Encodes Action Space
title_fullStr The Spatiotemporal Organization of the Striatum Encodes Action Space
title_full_unstemmed The Spatiotemporal Organization of the Striatum Encodes Action Space
title_short The Spatiotemporal Organization of the Striatum Encodes Action Space
title_sort spatiotemporal organization of the striatum encodes action space
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584673/
https://www.ncbi.nlm.nih.gov/pubmed/28858619
http://dx.doi.org/10.1016/j.neuron.2017.08.015
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