Please use this identifier to cite or link to this item: https://doi.org/10.7554/eLife.02536
DC FieldValue
dc.titleCerebellar modules operate at different frequencies
dc.contributor.authorZhou, H
dc.contributor.authorLin, Z
dc.contributor.authorVoges, K
dc.contributor.authorJu, C
dc.contributor.authorGao, Z
dc.contributor.authorBosman, L.W.J
dc.contributor.authorRuigrok, T.J
dc.contributor.authorHoebeek, F.E
dc.contributor.authorDe Zeeuw, C.I
dc.contributor.authorSchonewille, M
dc.date.accessioned2020-10-30T01:55:50Z
dc.date.available2020-10-30T01:55:50Z
dc.date.issued2014
dc.identifier.citationZhou, H, Lin, Z, Voges, K, Ju, C, Gao, Z, Bosman, L.W.J, Ruigrok, T.J, Hoebeek, F.E, De Zeeuw, C.I, Schonewille, M (2014). Cerebellar modules operate at different frequencies. eLife 2014 (3) : e02536. ScholarBank@NUS Repository. https://doi.org/10.7554/eLife.02536
dc.identifier.issn2050084X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/182023
dc.description.abstract24 Due to the uniform cyto-architecture of the cerebellar cortex, its overall physiological characteristics have traditionally been considered to be homogeneous. Here we show in awake mice at rest that spiking activity of Purkinje cells, the sole output cells of the cerebellar cortex, differs between cerebellar modules and correlates with their expression of the glycolytic enzyme aldolase C or zebrin. Simple spike and complex spike frequencies were significantly higher in Purkinje cells located in zebrin-negative than zebrin-positive modules. The difference in simple spike frequency persisted when the synaptic input to, but not intrinsic activity of, Purkinje cells was manipulated. Blocking TRPC3, the effector channel of a cascade of proteins that have zebrin-like distribution patterns, attenuated the simple spike frequency difference. Our results indicate that zebrin-discriminated cerebellar modules operate at different frequencies, which depends on activation of TRPC3, and that this property is relevant for all cerebellar functions.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectexcitatory amino acid transporter 4
dc.subjectfructose bisphosphate aldolase
dc.subjectmetabotropic receptor 1
dc.subjecttransient receptor potential channel 3
dc.subjectnerve protein
dc.subjecttransient receptor potential channel 3
dc.subjecttransient receptor potential channel C
dc.subjectzebrin I
dc.subjectadult
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectarticle
dc.subjectcell activity
dc.subjectcell population
dc.subjectcerebellum cortex
dc.subjectcerebellum nucleus
dc.subjectcontrolled study
dc.subjectelectrophysiological procedures
dc.subjectfemale
dc.subjectfluorescence microscopy
dc.subjectgene expression
dc.subjectimmunohistochemistry
dc.subjectinformation processing
dc.subjectlong term depression
dc.subjectlong term potentiation
dc.subjectmale
dc.subjectmouse
dc.subjectnerve cell excitability
dc.subjectnonhuman
dc.subjectprotein expression
dc.subjectPurkinje cell
dc.subjectspike wave
dc.subjectwhole cell patch clamp
dc.subjectaction potential
dc.subjectanimal
dc.subjectC57BL mouse
dc.subjectcerebellum cortex
dc.subjectcytology
dc.subjectmetabolism
dc.subjectphysiology
dc.subjectstaining
dc.subjectAction Potentials
dc.subjectAnimals
dc.subjectCerebellar Cortex
dc.subjectMale
dc.subjectMice, Inbred C57BL
dc.subjectNerve Tissue Proteins
dc.subjectPurkinje Cells
dc.subjectStaining and Labeling
dc.subjectTRPC Cation Channels
dc.typeArticle
dc.contributor.departmentLIFE SCIENCES INSTITUTE
dc.description.doi10.7554/eLife.02536
dc.description.sourcetitleeLife
dc.description.volume2014
dc.description.issue3
dc.description.pagee02536
Appears in Collections:Elements
Staff Publications

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_7554_eLife_02536.pdf2.37 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons