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  4. Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
 
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Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking
File(s)
s41467-017-00312-1.pdf (2.95 MB)
Published version
Author(s)
Chen, S
Augustine, GJ
Chadderton, PT
Type
Journal Article
Abstract
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.
Date Issued
2017-08-10
Date Acceptance
2017-06-21
Citation
Nature Communications, 2017, 8
URI
http://hdl.handle.net/10044/1/49624
DOI
https://www.dx.doi.org/10.1038/s41467-017-00312-1
ISSN
2041-1723
Publisher
Nature Publishing Group: Nature Communications
Journal / Book Title
Nature Communications
Volume
8
Copyright Statement
© The Author(s) 2017. Open Access
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/
Sponsor
Medical Research Council (MRC)
Human Frontier Science Program
Biotechnology and Biological Sciences Research Council (BBSRC)
Grant Number
G1000512
RGY089/2012
BB/N008871/1
Subjects
MD Multidisciplinary
Publication Status
Published
Article Number
232
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