| Literature DB >> 31486767 |
Bin Wu1, François Gc Blot1, Aaron Benson Wong1, Catarina Osório1, Youri Adolfs2, R Jeroen Pasterkamp2, Jana Hartmann3, Esther Be Becker4, Henk-Jan Boele1, Chris I De Zeeuw1,5, Martijn Schonewille1.
Abstract
Despite the canonical homogeneous character of its organization, the cerebellum plays differential computational roles in distinct sensorimotor behaviors. Previously, we showed that Purkinje cell (PC) activity differs between zebrin-negative (Z-) and zebrin-positive (Z+) modules (Zhou et al., 2014). Here, using gain-of-function and loss-of-function mouse models, we show that transient receptor potential cation channel C3 (TRPC3) controls the simple spike activity of Z-, but not Z+ PCs. In addition, TRPC3 regulates complex spike rate and their interaction with simple spikes, exclusively in Z- PCs. At the behavioral level, TRPC3 loss-of-function mice show impaired eyeblink conditioning, which is related to Z- modules, whereas compensatory eye movement adaptation, linked to Z+ modules, is intact. Together, our results indicate that TRPC3 is a major contributor to the cellular heterogeneity that introduces distinct physiological properties in PCs, conjuring functional heterogeneity in cerebellar sensorimotor integration.Entities:
Keywords: Purkinje cell; TRPC3; cellular heterogeneity; cerebellar function; mouse; neuroscience; spiking activity; zebrin/aldolase C
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Year: 2019 PMID: 31486767 PMCID: PMC6733575 DOI: 10.7554/eLife.45590
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140