Please use this identifier to cite or link to this item:
https://doi.org/10.7554/eLife.02536
DC Field | Value | |
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dc.title | Cerebellar modules operate at different frequencies | |
dc.contributor.author | Zhou, H | |
dc.contributor.author | Lin, Z | |
dc.contributor.author | Voges, K | |
dc.contributor.author | Ju, C | |
dc.contributor.author | Gao, Z | |
dc.contributor.author | Bosman, L.W.J | |
dc.contributor.author | Ruigrok, T.J | |
dc.contributor.author | Hoebeek, F.E | |
dc.contributor.author | De Zeeuw, C.I | |
dc.contributor.author | Schonewille, M | |
dc.date.accessioned | 2020-10-30T01:55:50Z | |
dc.date.available | 2020-10-30T01:55:50Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Zhou, 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.issn | 2050084X | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/182023 | |
dc.description.abstract | 24 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.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | excitatory amino acid transporter 4 | |
dc.subject | fructose bisphosphate aldolase | |
dc.subject | metabotropic receptor 1 | |
dc.subject | transient receptor potential channel 3 | |
dc.subject | nerve protein | |
dc.subject | transient receptor potential channel 3 | |
dc.subject | transient receptor potential channel C | |
dc.subject | zebrin I | |
dc.subject | adult | |
dc.subject | animal experiment | |
dc.subject | animal tissue | |
dc.subject | article | |
dc.subject | cell activity | |
dc.subject | cell population | |
dc.subject | cerebellum cortex | |
dc.subject | cerebellum nucleus | |
dc.subject | controlled study | |
dc.subject | electrophysiological procedures | |
dc.subject | female | |
dc.subject | fluorescence microscopy | |
dc.subject | gene expression | |
dc.subject | immunohistochemistry | |
dc.subject | information processing | |
dc.subject | long term depression | |
dc.subject | long term potentiation | |
dc.subject | male | |
dc.subject | mouse | |
dc.subject | nerve cell excitability | |
dc.subject | nonhuman | |
dc.subject | protein expression | |
dc.subject | Purkinje cell | |
dc.subject | spike wave | |
dc.subject | whole cell patch clamp | |
dc.subject | action potential | |
dc.subject | animal | |
dc.subject | C57BL mouse | |
dc.subject | cerebellum cortex | |
dc.subject | cytology | |
dc.subject | metabolism | |
dc.subject | physiology | |
dc.subject | staining | |
dc.subject | Action Potentials | |
dc.subject | Animals | |
dc.subject | Cerebellar Cortex | |
dc.subject | Male | |
dc.subject | Mice, Inbred C57BL | |
dc.subject | Nerve Tissue Proteins | |
dc.subject | Purkinje Cells | |
dc.subject | Staining and Labeling | |
dc.subject | TRPC Cation Channels | |
dc.type | Article | |
dc.contributor.department | LIFE SCIENCES INSTITUTE | |
dc.description.doi | 10.7554/eLife.02536 | |
dc.description.sourcetitle | eLife | |
dc.description.volume | 2014 | |
dc.description.issue | 3 | |
dc.description.page | e02536 | |
Appears in Collections: | Elements Staff Publications |
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