A non-canonical striatopallidal Go pathway that supports motor control

Marie A. Labouesse(New York Psychoanalytic Society and Institute), Arturo Torres-Herraez(New York Psychoanalytic Society and Institute), Muhammad O. Chohan(New York Psychoanalytic Society and Institute), Joseph M. Villarin(New York Psychoanalytic Society and Institute), Julia Greenwald(New York Psychoanalytic Society and Institute), Xiaoxiao Sun(New York Psychoanalytic Society and Institute), Mysarah Zahran(New York Psychoanalytic Society and Institute), Alice Tang(New York Psychoanalytic Society and Institute), Sherry Lam(National Institute on Drug Abuse), Jeremy Veenstra‐VanderWeele(New York Psychoanalytic Society and Institute), Clay Lacefield(New York Psychoanalytic Society and Institute), Jordi Bonaventura(National Institute on Drug Abuse), Michael Michaelides(National Institute on Drug Abuse), C. Savio Chan(Northwestern University), Ofer Yizhar(Weizmann Institute of Science), Christoph Kellendonk(Columbia University Irving Medical Center)
Nature Communications
October 23, 2023
Cited by 22Open Access
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Abstract

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 axon collaterals within the globus pallidus (GPe) (bridging collaterals), yet the significance of these collaterals for behavior is unknown. Here we use in vivo optical and chemogenetic tools combined with deep learning approaches in mice to dissect the roles of dSPN GPe 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 Npas1 neurons. We propose a model by which dSPN GPe axon collaterals (striatopallidal Go pathway) act in concert with the canonical terminals in the SNr to support motor control by inhibiting Npas1 neurons.


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