Granule cells reorient cortical manifolds to separate contexts but preserve their geometry

To learn effectively, animals must generalize across yet distinguish between related contexts. Generalization relies on low-dimensional neural manifolds found throughout neocortex <sup>1-3</sup> , which accelerate learning by constraining neural activity to task-relevant axes <sup>4,5</sup> . Conversely, context separation is attributed to neural expansion layers that can project information into high-dimensional feature spaces <sup>6-8</sup> , most famously cerebellar granule cells (GrCs) <sup>9-11</sup> . To investigate the generalization-separation tradeoff, we simultaneously imaged key nodes in the universal cortico-cerebellar pathway <sup>12,13</sup> -premotor layer 5 pyramidal tract (L5PT) and GrCs-during parallel learning of two distinct skills with shared temporal structure. Rather than expanding the cortical representations, GrCs retained their low-rank encoding of each task. Across contexts, however, despite stable cortico-cerebellar coupling, L5PT activity patterns generalized while GrC patterns temporally remapped. Mechanistically, GrCs used affine transformations that rotated the cortical manifolds apart but preserved their intrinsic low-dimensional geometry. Moreover, GrCs decorrelated cortical trajectories most strongly in expert animals. This reveals a fundamental architectural division of labor: the cortex generates invariant dynamic primitives for smooth generalization, while the cerebellum reconfigures them to drive context-specific output.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-03-04
DOI
https://doi.org/10.64898/2026.03.03.709240
Primary Topic
Vestibular and auditory disorders
Type
article
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article

Granule cells reorient cortical manifolds to separate contexts but preserve their geometry

Michał J. Wójcik, Amma Otchere, Lizmaylin Ramos, Martha G. Garcia-Garcia et al.
bioRxiv (Cold Spring Harbor Laboratory)
Vestibular and auditory disorders
article

Granule cells reorient cortical manifolds to separate contexts but preserve their geometry

Michał J. Wójcik, Amma Otchere, Lizmaylin Ramos, Martha G. Garcia-Garcia, Oluwatobi Akinwale, Rui Ponte Costa, Luke Drake, Srijan Thota
article en

Abstract

To learn effectively, animals must generalize across yet distinguish between related contexts. Generalization relies on low-dimensional neural manifolds found throughout neocortex <sup>1-3</sup> , which accelerate learning by constraining neural activity to task-relevant axes <sup>4,5</sup> . Conversely, context separation is attributed to neural expansion layers that can project information into high-dimensional feature spaces <sup>6-8</sup> , most famously cerebellar granule cells (GrCs) <sup>9-11</sup> . To investigate the generalization-separation tradeoff, we simultaneously imaged key nodes in the universal cortico-cerebellar pathway <sup>12,13</sup> -premotor layer 5 pyramidal tract (L5PT) and GrCs-during parallel learning of two distinct skills with shared temporal structure. Rather than expanding the cortical representations, GrCs retained their low-rank encoding of each task. Across contexts, however, despite stable cortico-cerebellar coupling, L5PT activity patterns generalized while GrC patterns temporally remapped. Mechanistically, GrCs used affine transformations that rotated the cortical manifolds apart but preserved their intrinsic low-dimensional geometry. Moreover, GrCs decorrelated cortical trajectories most strongly in expert animals. This reveals a fundamental architectural division of labor: the cortex generates invariant dynamic primitives for smooth generalization, while the cerebellum reconfigures them to drive context-specific output.

bioRxiv (Cold Spring Harbor Laboratory)
National Institutes of Health (US), University of Oxford (GB), National Institute of Neurological Disorders and Stroke (US)
Decent work and economic growth
Openalex Percentile: Top 47%
Vestibular and auditory disorders
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