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A non-canonical striatopallidal “Go” pathway that supports motor control

In the classical model of the basal ganglia, direct pathway striatal projection neurons (dSPNs) send projections to the substantia nigra (SNr) and entopeduncular nucleus to regulate motor function. Recent studies have re-established that dSPNs also possess “bridging” collaterals within the globus pa...

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Autores principales: Labouesse, Marie A., Torres-Herraez, Arturo, Chohan, Muhammad O., Villarin, Joseph, Greenwald, Julia, Sun, Xiaoxiao, Zahran, Mysarah, Tang, Alice, Lam, Sherry, Veenstra-VanderWeele, Jeremy, Lacefield, Clay, Bonaventura, Jordi, Michaelides, Michael, Chan, C. Savio, Yizhar, Ofer, Kellendonk, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934763/
https://www.ncbi.nlm.nih.gov/pubmed/36798372
http://dx.doi.org/10.21203/rs.3.rs-2524816/v1
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author Labouesse, Marie A.
Torres-Herraez, Arturo
Chohan, Muhammad O.
Villarin, Joseph
Greenwald, Julia
Sun, Xiaoxiao
Zahran, Mysarah
Tang, Alice
Lam, Sherry
Veenstra-VanderWeele, Jeremy
Lacefield, Clay
Bonaventura, Jordi
Michaelides, Michael
Chan, C. Savio
Yizhar, Ofer
Kellendonk, Christoph
author_facet Labouesse, Marie A.
Torres-Herraez, Arturo
Chohan, Muhammad O.
Villarin, Joseph
Greenwald, Julia
Sun, Xiaoxiao
Zahran, Mysarah
Tang, Alice
Lam, Sherry
Veenstra-VanderWeele, Jeremy
Lacefield, Clay
Bonaventura, Jordi
Michaelides, Michael
Chan, C. Savio
Yizhar, Ofer
Kellendonk, Christoph
author_sort Labouesse, Marie A.
collection PubMed
description In the classical model of the basal ganglia, direct pathway striatal projection neurons (dSPNs) send projections to the substantia nigra (SNr) and entopeduncular nucleus to regulate motor function. Recent studies have re-established that dSPNs also possess “bridging” collaterals within the globus pallidus (GPe), yet the significance of these collaterals for behavior is unknown. Here we use in vivo optical and chemogenetic tools combined with deep learning approaches to dissect the roles of bridging collaterals in motor function. We find that dSPNs projecting to the SNr send synchronous motor-related information to the GPe via axon collaterals. Inhibition of native activity in dSPN GPe terminals impairs motor activity and function via regulation of pallidostriatal Npas1 neurons. We propose a model by which dSPN GPe collaterals (“striatopallidal Go pathway”) act in concert with the canonical terminals in the SNr to support motor control by inhibiting Npas1 signals going back to the striatum.
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spelling pubmed-99347632023-02-17 A non-canonical striatopallidal “Go” pathway that supports motor control Labouesse, Marie A. Torres-Herraez, Arturo Chohan, Muhammad O. Villarin, Joseph Greenwald, Julia Sun, Xiaoxiao Zahran, Mysarah Tang, Alice Lam, Sherry Veenstra-VanderWeele, Jeremy Lacefield, Clay Bonaventura, Jordi Michaelides, Michael Chan, C. Savio Yizhar, Ofer Kellendonk, Christoph Res Sq Article In the classical model of the basal ganglia, direct pathway striatal projection neurons (dSPNs) send projections to the substantia nigra (SNr) and entopeduncular nucleus to regulate motor function. Recent studies have re-established that dSPNs also possess “bridging” collaterals within the globus pallidus (GPe), yet the significance of these collaterals for behavior is unknown. Here we use in vivo optical and chemogenetic tools combined with deep learning approaches to dissect the roles of bridging collaterals in motor function. We find that dSPNs projecting to the SNr send synchronous motor-related information to the GPe via axon collaterals. Inhibition of native activity in dSPN GPe terminals impairs motor activity and function via regulation of pallidostriatal Npas1 neurons. We propose a model by which dSPN GPe collaterals (“striatopallidal Go pathway”) act in concert with the canonical terminals in the SNr to support motor control by inhibiting Npas1 signals going back to the striatum. American Journal Experts 2023-02-11 /pmc/articles/PMC9934763/ /pubmed/36798372 http://dx.doi.org/10.21203/rs.3.rs-2524816/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. https://creativecommons.org/licenses/by/4.0/License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Labouesse, Marie A.
Torres-Herraez, Arturo
Chohan, Muhammad O.
Villarin, Joseph
Greenwald, Julia
Sun, Xiaoxiao
Zahran, Mysarah
Tang, Alice
Lam, Sherry
Veenstra-VanderWeele, Jeremy
Lacefield, Clay
Bonaventura, Jordi
Michaelides, Michael
Chan, C. Savio
Yizhar, Ofer
Kellendonk, Christoph
A non-canonical striatopallidal “Go” pathway that supports motor control
title A non-canonical striatopallidal “Go” pathway that supports motor control
title_full A non-canonical striatopallidal “Go” pathway that supports motor control
title_fullStr A non-canonical striatopallidal “Go” pathway that supports motor control
title_full_unstemmed A non-canonical striatopallidal “Go” pathway that supports motor control
title_short A non-canonical striatopallidal “Go” pathway that supports motor control
title_sort non-canonical striatopallidal “go” pathway that supports motor control
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934763/
https://www.ncbi.nlm.nih.gov/pubmed/36798372
http://dx.doi.org/10.21203/rs.3.rs-2524816/v1
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