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Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium.


ABSTRACT: Climbing fibers (CFs) generate complex spikes (CS) and Ca2+ transients in cerebellar Purkinje cells (PCs), serving as instructive signals. The so-called 'all-or-none' character of CSs has been questioned since the CF burst was described. Although recent studies have indicated a sensory-driven enhancement of PC Ca2+ signals, how CF responds to sensory events and contributes to PC dendritic Ca2+ and CS remains unexplored. Here, single or simultaneous Ca2+ imaging of CFs and PCs in awake mice revealed the presynaptic CF Ca2+ amplitude encoded the sensory input's strength and directly influenced post-synaptic PC dendritic Ca2+ amplitude. The sensory-driven variability in CF Ca2+ amplitude depended on the number of spikes in the CF burst. Finally, the spike number of the CF burst determined the PC Ca2+ influx and CS properties. These results reveal the direct translation of sensory information-coding CF inputs into PC Ca2+, suggesting the sophisticated role of CFs as error signals.

SUBMITTER: Roh SE 

PROVIDER: S-EPMC7581426 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

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Direct translation of climbing fiber burst-mediated sensory coding into post-synaptic Purkinje cell dendritic calcium.

Roh Seung-Eon SE   Kim Seung Ha SH   Ryu Changhyeon C   Kim Chang-Eop CE   Kim Yong Gyu YG   Worley Paul F PF   Kim Sun Kwang SK   Kim Sang Jeong SJ  

eLife 20200928


Climbing fibers (CFs) generate complex spikes (CS) and Ca<sup>2+</sup> transients in cerebellar Purkinje cells (PCs), serving as instructive signals. The so-called 'all-or-none' character of CSs has been questioned since the CF burst was described. Although recent studies have indicated a sensory-driven enhancement of PC Ca<sup>2+</sup> signals, how CF responds to sensory events and contributes to PC dendritic Ca<sup>2+</sup> and CS remains unexplored. Here, single or simultaneous Ca<sup>2+</sup  ...[more]

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