Ground-truth encoding of self-motion in the primate cerebellar nodulus and uvula

Accurate internal estimates of self-motion and orientation relative to gravity are fundamental for stabilizing gaze, controlling posture, and navigating through dynamic environments. Prevailing theories propose that the cerebellar nodulus and uvula (NU) employ internal models to suppress sensory input arising from predictable, self-generated motion. However, this assumption has never been directly tested. Here, we recorded NU Purkinje cell activity in rhesus monkeys during active and passive head movements. We found neurons responsive to passive translations remained equally sensitive to self-generated movements, encoding net head motion in space irrespective of its source. Furthermore, external perturbation did not influence these ground-truth encoding. When active head motion was blocked, Purkinje cell activity remained unchanged - demonstrating a lack of efference copy integration. During active tilts, NU neurons encoded both dynamic motion and static orientation relative to gravity. These findings challenge the internal model hypothesis and establish the NU as a ground-truth, context-invariant estimator of self-motion, supporting stable behavior in dynamic environments.

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Publication Details

Journal
Nature Communications
Published
2026-02-25
DOI
https://doi.org/10.1038/s41467-026-69909-9
Primary Topic
Vestibular and auditory disorders
Type
article
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article

Ground-truth encoding of self-motion in the primate cerebellar nodulus and uvula

Kathleen E. Cullen, Robyn L. Mildren
Nature Communications
Vestibular and auditory disorders
article

Ground-truth encoding of self-motion in the primate cerebellar nodulus and uvula

Kathleen E. Cullen, Robyn L. Mildren
article en

Abstract

Accurate internal estimates of self-motion and orientation relative to gravity are fundamental for stabilizing gaze, controlling posture, and navigating through dynamic environments. Prevailing theories propose that the cerebellar nodulus and uvula (NU) employ internal models to suppress sensory input arising from predictable, self-generated motion. However, this assumption has never been directly tested. Here, we recorded NU Purkinje cell activity in rhesus monkeys during active and passive head movements. We found neurons responsive to passive translations remained equally sensitive to self-generated movements, encoding net head motion in space irrespective of its source. Furthermore, external perturbation did not influence these ground-truth encoding. When active head motion was blocked, Purkinje cell activity remained unchanged - demonstrating a lack of efference copy integration. During active tilts, NU neurons encoded both dynamic motion and static orientation relative to gravity. These findings challenge the internal model hypothesis and establish the NU as a ground-truth, context-invariant estimator of self-motion, supporting stable behavior in dynamic environments.

Nature Communications
Johns Hopkins University (US), Johns Hopkins Medicine (US), University of Baltimore (US)
Openalex Percentile: Top 55%
Vestibular and auditory disorders
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