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https://doi.org/10.1038/s41467-017-00312-1
Title: | Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking | Authors: | Chen, S Augustine, G.J Chadderton, P |
Keywords: | brain cells and cell components inhibitor kinematics molecular analysis nervous system animal behavior animal experiment Article cell population cerebellum cerebellum cortex cerebellum molecular layer current clamp technique downstream processing electrophysiological procedures excitatory postsynaptic potential female firing rate granule cell in vivo study interneuron kinematics male mouse movement (physiology) nerve cell membrane steady potential nerve cell stimulation neuromodulation nonhuman patch clamp technique Purkinje cell signal processing synaptic inhibition tuning curve voltage clamp technique voluntary movement whisker movement animal C57BL mouse cell culture cerebellum chemistry cytology electrophysiology nerve cell physiology Animals Cells, Cultured Cerebellum Electrophysiology Interneurons Mice Mice, Inbred C57BL Neurons Purkinje Cells |
Issue Date: | 2017 | Publisher: | Nature Publishing Group | Citation: | Chen, S, Augustine, G.J, Chadderton, P (2017). Serial processing of kinematic signals by cerebellar circuitry during voluntary whisking. Nature Communications 8 (1) : 312. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-017-00312-1 | Rights: | Attribution 4.0 International | 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. © 2017 The Author(s). | Source Title: | Nature Communications | URI: | https://scholarbank.nus.edu.sg/handle/10635/178593 | ISSN: | 2041-1723 | DOI: | 10.1038/s41467-017-00312-1 | Rights: | Attribution 4.0 International |
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