Transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortex

Sensory signals undergo substantial recoding when neural activity is relayed from sensors through pre-thalamic and thalamic nuclei to cortex. To explore how temporal dynamics and directional tuning are sculpted in hierarchical vestibular circuits, we compared responses of macaque otolith afferents w...

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Main Authors: Jean Laurens, Sheng Liu, Xiong-Jie Yu, Raymond Chan, David Dickman, Gregory C DeAngelis, Dora E Angelaki
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2017-01-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/20787
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spelling doaj-1e6772d6063246488734c2acf77b0f702021-05-05T13:10:41ZengeLife Sciences Publications LtdeLife2050-084X2017-01-01610.7554/eLife.20787Transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortexJean Laurens0https://orcid.org/0000-0002-9101-2802Sheng Liu1Xiong-Jie Yu2Raymond Chan3David Dickman4Gregory C DeAngelis5https://orcid.org/0000-0002-1635-1273Dora E Angelaki6https://orcid.org/0000-0002-9650-8962Department of Neuroscience, Baylor College of Medicine, Houston, United StatesState Key Laboratory of Ophthalmology, Zhongshan Opthalmic Center, Sun Yat-sen University, Guangzhou, ChinaDepartment of Neuroscience, Baylor College of Medicine, Houston, United States; Zhejiang University Interdisciplinary Institute of Neuroscience and Technology, Zhejiang University, Hangzhou, China; Qiushi Academy for Advanced Studies, Zhejiang University, Hangzhou, ChinaDepartment of Neuroscience, Baylor College of Medicine, Houston, United StatesDepartment of Neuroscience, Baylor College of Medicine, Houston, United StatesDeptartment of Brain and Cognitive Sciences, University of Rochester, Rochester, United StatesDepartment of Neuroscience, Baylor College of Medicine, Houston, United StatesSensory signals undergo substantial recoding when neural activity is relayed from sensors through pre-thalamic and thalamic nuclei to cortex. To explore how temporal dynamics and directional tuning are sculpted in hierarchical vestibular circuits, we compared responses of macaque otolith afferents with neurons in the vestibular and cerebellar nuclei, as well as five cortical areas, to identical three-dimensional translational motion. We demonstrate a remarkable spatio-temporal transformation: otolith afferents carry spatially aligned cosine-tuned translational acceleration and jerk signals. In contrast, brainstem and cerebellar neurons exhibit non-linear, mixed selectivity for translational velocity, acceleration, jerk and position. Furthermore, these components often show dissimilar spatial tuning. Moderate further transformation of translation signals occurs in the cortex, such that similar spatio-temporal properties are found in multiple cortical areas. These results suggest that the first synapse represents a key processing element in vestibular pathways, robustly shaping how self-motion is represented in central vestibular circuits and cortical areas.https://elifesciences.org/articles/20787vestibularbrainstemcerebellumcortex
collection DOAJ
language English
format Article
sources DOAJ
author Jean Laurens
Sheng Liu
Xiong-Jie Yu
Raymond Chan
David Dickman
Gregory C DeAngelis
Dora E Angelaki
spellingShingle Jean Laurens
Sheng Liu
Xiong-Jie Yu
Raymond Chan
David Dickman
Gregory C DeAngelis
Dora E Angelaki
Transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortex
eLife
vestibular
brainstem
cerebellum
cortex
author_facet Jean Laurens
Sheng Liu
Xiong-Jie Yu
Raymond Chan
David Dickman
Gregory C DeAngelis
Dora E Angelaki
author_sort Jean Laurens
title Transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortex
title_short Transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortex
title_full Transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortex
title_fullStr Transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortex
title_full_unstemmed Transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortex
title_sort transformation of spatiotemporal dynamics in the macaque vestibular system from otolith afferents to cortex
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2017-01-01
description Sensory signals undergo substantial recoding when neural activity is relayed from sensors through pre-thalamic and thalamic nuclei to cortex. To explore how temporal dynamics and directional tuning are sculpted in hierarchical vestibular circuits, we compared responses of macaque otolith afferents with neurons in the vestibular and cerebellar nuclei, as well as five cortical areas, to identical three-dimensional translational motion. We demonstrate a remarkable spatio-temporal transformation: otolith afferents carry spatially aligned cosine-tuned translational acceleration and jerk signals. In contrast, brainstem and cerebellar neurons exhibit non-linear, mixed selectivity for translational velocity, acceleration, jerk and position. Furthermore, these components often show dissimilar spatial tuning. Moderate further transformation of translation signals occurs in the cortex, such that similar spatio-temporal properties are found in multiple cortical areas. These results suggest that the first synapse represents a key processing element in vestibular pathways, robustly shaping how self-motion is represented in central vestibular circuits and cortical areas.
topic vestibular
brainstem
cerebellum
cortex
url https://elifesciences.org/articles/20787
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