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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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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. |
format | Online Article Text |
id | pubmed-5584673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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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