Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking

Purkinje cells (PCs) in Crus 1 represent whisker movement via linear changes in firing rate, but the circuit mechanisms underlying this coding scheme are unknown. Here we examine the role of upstream inputs to PCs—excitatory granule cells (GCs) and inhibitory molecular layer interneurons—in processi...

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Main Authors: Chen, Susu, Augustine, George James, Chadderton, Paul
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2018
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Online Access:https://hdl.handle.net/10356/89516
http://hdl.handle.net/10220/44970
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-895162020-11-01T05:17:22Z Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking Chen, Susu Augustine, George James Chadderton, Paul Lee Kong Chian School of Medicine (LKCMedicine) Neuromodulation Signal Processing Purkinje cells (PCs) in Crus 1 represent whisker movement via linear changes in firing rate, but the circuit mechanisms underlying this coding scheme are unknown. Here we examine the role of upstream inputs to PCs—excitatory granule cells (GCs) and inhibitory molecular layer interneurons—in processing of whisking signals. Patch clamp recordings in GCs reveal that movement is accompanied by changes in mossy fibre input rate that drive membrane potential depolarisation and high-frequency bursting activity at preferred whisker angles. Although individual GCs are narrowly tuned, GC populations provide linear excitatory drive across a wide range of movement. Molecular layer interneurons exhibit bidirectional firing rate changes during whisking, similar to PCs. Together, GC populations provide downstream PCs with linear representations of volitional movement, while inhibitory networks invert these signals. The exquisite sensitivity of neurons at each processing stage enables faithful propagation of kinematic representations through the cerebellum. NRF (Natl Research Foundation, S’pore) Published version 2018-06-06T04:01:05Z 2019-12-06T17:27:27Z 2018-06-06T04:01:05Z 2019-12-06T17:27:27Z 2017 Journal Article Chen, S., Augustine, G. J., & Chadderton, P. (2017). Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking. Nature Communications, 8(1), 232-. 2041-1723 https://hdl.handle.net/10356/89516 http://hdl.handle.net/10220/44970 10.1038/s41467-017-00312-1 en Nature Communications © 2017 The Author(s). This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ 13 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Neuromodulation
Signal Processing
spellingShingle Neuromodulation
Signal Processing
Chen, Susu
Augustine, George James
Chadderton, Paul
Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
description Purkinje cells (PCs) in Crus 1 represent whisker movement via linear changes in firing rate, but the circuit mechanisms underlying this coding scheme are unknown. Here we examine the role of upstream inputs to PCs—excitatory granule cells (GCs) and inhibitory molecular layer interneurons—in processing of whisking signals. Patch clamp recordings in GCs reveal that movement is accompanied by changes in mossy fibre input rate that drive membrane potential depolarisation and high-frequency bursting activity at preferred whisker angles. Although individual GCs are narrowly tuned, GC populations provide linear excitatory drive across a wide range of movement. Molecular layer interneurons exhibit bidirectional firing rate changes during whisking, similar to PCs. Together, GC populations provide downstream PCs with linear representations of volitional movement, while inhibitory networks invert these signals. The exquisite sensitivity of neurons at each processing stage enables faithful propagation of kinematic representations through the cerebellum.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Chen, Susu
Augustine, George James
Chadderton, Paul
format Article
author Chen, Susu
Augustine, George James
Chadderton, Paul
author_sort Chen, Susu
title Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
title_short Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
title_full Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
title_fullStr Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
title_full_unstemmed Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
title_sort serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
publishDate 2018
url https://hdl.handle.net/10356/89516
http://hdl.handle.net/10220/44970
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