Distinct representations of body and head motion are dynamically encoded by Purkinje cell populations in the macaque cerebellum

The ability to accurately control our posture and perceive our spatial orientation during self-motion requires knowledge of the motion of both the head and body. However, while the vestibular sensors and nuclei directly encode head motion, no sensors directly encode body motion. Instead, the integra...

Full description

Bibliographic Details
Main Authors: Omid A Zobeiri, Kathleen E Cullen
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2022-04-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/75018
_version_ 1818026286291877888
author Omid A Zobeiri
Kathleen E Cullen
author_facet Omid A Zobeiri
Kathleen E Cullen
author_sort Omid A Zobeiri
collection DOAJ
description The ability to accurately control our posture and perceive our spatial orientation during self-motion requires knowledge of the motion of both the head and body. However, while the vestibular sensors and nuclei directly encode head motion, no sensors directly encode body motion. Instead, the integration of vestibular and neck proprioceptive inputs is necessary to transform vestibular information into the body-centric reference frame required for postural control. The anterior vermis of the cerebellum is thought to play a key role in this transformation, yet how its Purkinje cells transform multiple streams of sensory information into an estimate of body motion remains unknown. Here, we recorded the activity of individual anterior vermis Purkinje cells in alert monkeys during passively applied whole-body, body-under-head, and head-on-body rotations. Most Purkinje cells dynamically encoded an intermediate representation of self-motion between head and body motion. Notably, Purkinje cells responded to both vestibular and neck proprioceptive stimulation with considerable heterogeneity in their response dynamics. Furthermore, their vestibular responses were tuned to head-on-body position. In contrast, targeted neurons in the deep cerebellar nuclei are known to unambiguously encode either head or body motion across conditions. Using a simple population model, we established that combining responses of~40-50 Purkinje cells could explain the responses of these deep cerebellar nuclei neurons across all self-motion conditions. We propose that the observed heterogeneity in Purkinje cell response dynamics underlies the cerebellum’s capacity to compute the dynamic representation of body motion required to ensure accurate postural control and perceptual stability in our daily lives.
first_indexed 2024-12-10T04:29:35Z
format Article
id doaj.art-a70c566c918f42f08d2c6f0e0db8ea14
institution Directory Open Access Journal
issn 2050-084X
language English
last_indexed 2024-12-10T04:29:35Z
publishDate 2022-04-01
publisher eLife Sciences Publications Ltd
record_format Article
series eLife
spelling doaj.art-a70c566c918f42f08d2c6f0e0db8ea142022-12-22T02:02:11ZengeLife Sciences Publications LtdeLife2050-084X2022-04-011110.7554/eLife.75018Distinct representations of body and head motion are dynamically encoded by Purkinje cell populations in the macaque cerebellumOmid A Zobeiri0https://orcid.org/0000-0002-1813-1354Kathleen E Cullen1https://orcid.org/0000-0002-9348-0933Department of Biomedical Engineering, McGill University, Montreal, CanadaDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, United States; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, United States; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, United States; Kavli Neuroscience Discovery Institute, Johns Hopkins University, Baltimore, United StatesThe ability to accurately control our posture and perceive our spatial orientation during self-motion requires knowledge of the motion of both the head and body. However, while the vestibular sensors and nuclei directly encode head motion, no sensors directly encode body motion. Instead, the integration of vestibular and neck proprioceptive inputs is necessary to transform vestibular information into the body-centric reference frame required for postural control. The anterior vermis of the cerebellum is thought to play a key role in this transformation, yet how its Purkinje cells transform multiple streams of sensory information into an estimate of body motion remains unknown. Here, we recorded the activity of individual anterior vermis Purkinje cells in alert monkeys during passively applied whole-body, body-under-head, and head-on-body rotations. Most Purkinje cells dynamically encoded an intermediate representation of self-motion between head and body motion. Notably, Purkinje cells responded to both vestibular and neck proprioceptive stimulation with considerable heterogeneity in their response dynamics. Furthermore, their vestibular responses were tuned to head-on-body position. In contrast, targeted neurons in the deep cerebellar nuclei are known to unambiguously encode either head or body motion across conditions. Using a simple population model, we established that combining responses of~40-50 Purkinje cells could explain the responses of these deep cerebellar nuclei neurons across all self-motion conditions. We propose that the observed heterogeneity in Purkinje cell response dynamics underlies the cerebellum’s capacity to compute the dynamic representation of body motion required to ensure accurate postural control and perceptual stability in our daily lives.https://elifesciences.org/articles/75018cerebellumPurkinje cellsvestibularproprioceptionneurophysiologypopulation coding
spellingShingle Omid A Zobeiri
Kathleen E Cullen
Distinct representations of body and head motion are dynamically encoded by Purkinje cell populations in the macaque cerebellum
eLife
cerebellum
Purkinje cells
vestibular
proprioception
neurophysiology
population coding
title Distinct representations of body and head motion are dynamically encoded by Purkinje cell populations in the macaque cerebellum
title_full Distinct representations of body and head motion are dynamically encoded by Purkinje cell populations in the macaque cerebellum
title_fullStr Distinct representations of body and head motion are dynamically encoded by Purkinje cell populations in the macaque cerebellum
title_full_unstemmed Distinct representations of body and head motion are dynamically encoded by Purkinje cell populations in the macaque cerebellum
title_short Distinct representations of body and head motion are dynamically encoded by Purkinje cell populations in the macaque cerebellum
title_sort distinct representations of body and head motion are dynamically encoded by purkinje cell populations in the macaque cerebellum
topic cerebellum
Purkinje cells
vestibular
proprioception
neurophysiology
population coding
url https://elifesciences.org/articles/75018
work_keys_str_mv AT omidazobeiri distinctrepresentationsofbodyandheadmotionaredynamicallyencodedbypurkinjecellpopulationsinthemacaquecerebellum
AT kathleenecullen distinctrepresentationsofbodyandheadmotionaredynamicallyencodedbypurkinjecellpopulationsinthemacaquecerebellum