Striatal ensembles specify and control granular forelimb actions

The ability of the brain to control specific fine actions is crucial for survival. The striatum is a critical brain center for both movement and learning, and its dysfunction underlies numerous movement disorders<sup>1-9</sup>. Whereas activity in the striatum has been classically viewed as invigorating<sup>5,10-13</sup> and reinforcing movements<sup>12-20</sup>, recent studies suggest that striatal activity encodes specific movements<sup>21-24</sup>. However, it is not known how granular this activity is, and if it indeed controls specific ongoing movements. We designed a task where mice performed two minimally-different forelimb actions, consisting of a push or pull isometric force on an immobile joystick, and imaged the activity of medium spiny neurons (MSNs) in the dorsolateral striatum using 2-photon microscopy. We observed that striatal activity encoded both the preparation and execution of specific actions, even when those actions were not reinforced. Furthermore, both populations of D1 and D2-MSNs - classically viewed as promoting versus inhibiting movement<sup>2,3,25</sup> - equally encoded action identity. We developed a closed-loop system to model and stimulate action-specific neural ensembles deep in the brain, using holographic optogenetics through a GRIN lens. Stimulation of action-specific ensembles of both D1- and D2-MSNs increased the force of ongoing actions, but only when the ensemble stimulated was congruent with the ongoing action. These results reveal that specific ensembles of both D1- and D2-MSNs causally control specific ongoing actions, as granular as different muscle co-contractions of the same forelimb. Such granularity provides a mechanistic framework for understanding how striatal dysfunction can produce highly specific movement impairments in Huntington's disease<sup>2,9</sup> and dystonia<sup>2,6</sup>.

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Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2025-12-08
DOI
https://doi.org/10.64898/2025.12.03.692128
Primary Topic
Neurological disorders and treatments
Type
article
Field-Weighted Citation Impact
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article

Striatal ensembles specify and control granular forelimb actions

Darcy S. Peterka, Rui M. Costa, Vivek R. Athalye, Ines Rodrigues-Vaz
bioRxiv (Cold Spring Harbor Laboratory)
Neurological disorders and treatments
article

Striatal ensembles specify and control granular forelimb actions

Darcy S. Peterka, Rui M. Costa, Vivek R. Athalye, Ines Rodrigues-Vaz
article en

Abstract

The ability of the brain to control specific fine actions is crucial for survival. The striatum is a critical brain center for both movement and learning, and its dysfunction underlies numerous movement disorders<sup>1-9</sup>. Whereas activity in the striatum has been classically viewed as invigorating<sup>5,10-13</sup> and reinforcing movements<sup>12-20</sup>, recent studies suggest that striatal activity encodes specific movements<sup>21-24</sup>. However, it is not known how granular this activity is, and if it indeed controls specific ongoing movements. We designed a task where mice performed two minimally-different forelimb actions, consisting of a push or pull isometric force on an immobile joystick, and imaged the activity of medium spiny neurons (MSNs) in the dorsolateral striatum using 2-photon microscopy. We observed that striatal activity encoded both the preparation and execution of specific actions, even when those actions were not reinforced. Furthermore, both populations of D1 and D2-MSNs - classically viewed as promoting versus inhibiting movement<sup>2,3,25</sup> - equally encoded action identity. We developed a closed-loop system to model and stimulate action-specific neural ensembles deep in the brain, using holographic optogenetics through a GRIN lens. Stimulation of action-specific ensembles of both D1- and D2-MSNs increased the force of ongoing actions, but only when the ensemble stimulated was congruent with the ongoing action. These results reveal that specific ensembles of both D1- and D2-MSNs causally control specific ongoing actions, as granular as different muscle co-contractions of the same forelimb. Such granularity provides a mechanistic framework for understanding how striatal dysfunction can produce highly specific movement impairments in Huntington's disease<sup>2,9</sup> and dystonia<sup>2,6</sup>.

bioRxiv (Cold Spring Harbor Laboratory)
Champalimaud Foundation (PT), Allen Institute for Brain Science (US), Allen Institute (US), Research Network (United States) (US), Columbia University (US)
Openalex Percentile: Top 46%
Neurological disorders and treatments
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