Coordinated cerebellar climbing fiber activity signals learned sensorimotor predictions

Nat Neurosci. 2018 Oct;21(10):1431-1441. doi: 10.1038/s41593-018-0228-8. Epub 2018 Sep 17.

Abstract

The prevailing model of cerebellar learning states that climbing fibers (CFs) are both driven by, and serve to correct, erroneous motor output. However, this model is grounded largely in studies of behaviors that utilize hardwired neural pathways to link sensory input to motor output. To test whether this model applies to more flexible learning regimes that require arbitrary sensorimotor associations, we developed a cerebellar-dependent motor learning task that is compatible with both mesoscale and single-dendrite-resolution calcium imaging in mice. We found that CFs were preferentially driven by and more time-locked to correctly executed movements and other task parameters that predict reward outcome, exhibiting widespread correlated activity in parasagittal processing zones that was governed by these predictions. Together, our data suggest that such CF activity patterns are well-suited to drive learning by providing predictive instructional input that is consistent with an unsigned reinforcement learning signal but does not rely exclusively on motor errors.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Animals
  • Calcium / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Cerebellum / physiology*
  • Excitatory Amino Acid Agents / pharmacology
  • Glycine / analogs & derivatives
  • Glycine / pharmacology
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / metabolism
  • Learning / drug effects
  • Learning / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Motor Activity / drug effects
  • Motor Activity / physiology*
  • Nerve Fibers / physiology*
  • Neural Pathways / drug effects
  • Neural Pathways / physiology*
  • Neurons / drug effects
  • Neurons / physiology*
  • Neuropeptides / genetics
  • Neuropeptides / metabolism
  • Principal Component Analysis
  • Pyrazines / pharmacology
  • Reaction Time / physiology
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology

Substances

  • Excitatory Amino Acid Agents
  • Guanine Nucleotide Exchange Factors
  • Neuropeptides
  • Pcp2 protein, mouse
  • Pyrazines
  • methyl-(4-carboxyphenyl)glycine
  • 6-chloro-2-(1-piperazinyl)pyrazine
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Calcium
  • Glycine