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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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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