Cerebellar modules operate at different frequencies
Haibo Zhou,
Zhanmin Lin,
Kai Voges,
Chiheng Ju,
Zhenyu Gao,
Laurens WJ Bosman,
Tom JH Ruigrok,
Freek E Hoebeek,
Chris I De Zeeuw,
Martijn Schonewille
Affiliations
Haibo Zhou
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Zhanmin Lin
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Kai Voges
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Chiheng Ju
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Zhenyu Gao
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Laurens WJ Bosman
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Tom JH Ruigrok
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Freek E Hoebeek
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Chris I De Zeeuw
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands; Cerebellar Coordination and Cognition, Netherlands Institute for Neuroscience, Amsterdam, Netherlands
Martijn Schonewille
Department of Neuroscience, Erasmus MC, Rotterdam, Netherlands
Due to the uniform cyto-architecture of the cerebellar cortex, its overall physiological characteristics have traditionally been considered to be homogeneous. In this study, 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 depend on activation of TRPC3, and that this property is relevant for all cerebellar functions.