Evidence map›Paper›PMID 40848722›Full record

ArticleCurrent biology : CB2025

Reward-driven cerebellar climbing fiber activity influences both neural and behavioral learning.

Shuyang Jin, Court Hull

Abstract read
In one paragraph

Article in Current biology : CB, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Consensus Paper: Models of Cerebellar Functions.Cerebellum (London, England) · 2026
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Shuyang JinDepartment of Neurobiology, Duke University, Durham, NC 27710, USA.
Court HullDepartment of Neurobiology, Duke University, Durham, NC 27710, USA. Electronic address: hull@neuro.duke.edu.

Funding

Canonical computations for motor learning by the cerebellar cortex micro-circuitR01NS112917 · NINDS · DUKE UNIVERSITY · PI LISBERGER, STEPHEN G, MEDINA, JAVIER F · 2019 to 2023
$6.4M
Cerebellar circuits for reward-based learningR01NS128054 · NINDS · DUKE UNIVERSITY · PI COURT A HULL · 2022 to 2026
$1.9M
Neuromodulatory Control of Cerebellar Synaptic Processing and Sensory InputR01NS096289 · NINDS · DUKE UNIVERSITY · PI HULL, COURT A · 2016 to 2020
$1.7M
NINDS NIH HHS R01 NS096289NINDS NIH HHS R01 NS112917NINDS NIH HHS R01 NS128054
6 · The paper itself

Abstract

The cerebellum plays a key role in motor coordination and learning. In contrast to classical supervised learning models, recent work has revealed that climbing fibers (CFs) can signal reward-predictive information in some behaviors. This raises the question of whether CFs may also operate according to the principles of reinforcement learning. To test how CFs operate during reward-guided behavior and evaluate the role of reward-related CF activity in learning, we measured CF responses in Purkinje cells of the lateral cerebellum during a Pavlovian task using two-photon calcium imaging. Specifically, we have performed multi-stimulus experiments to determine whether CF activity meets the requirements of a reward prediction error (rPE) signal for transfer from an unexpected reward to a reward-predictive cue. We find that once CF activity is transferred to a conditioned stimulus, and there is no longer a response to reward, CFs cannot generate learned responses to a second conditioned stimulus that carries the same reward prediction. In addition, by expressing the inhibitory opsin GtACR2 in neurons of the inferior olive and optically inhibiting these neurons during behavioral training at the time of unexpected reward, we find that the transfer of CF signals to the conditioned stimulus is impaired. Moreover, this optogenetic inhibition also impairs learning, resulting in a deficit in anticipatory lick timing. Together, these results indicate that CF signals can exhibit several characteristics in common with the rPEs that have been observed during reinforcement learning and that the cerebellum can harness these reward-related learning signals to generate accurately timed motor behavior.

Indexed as

CerebellumConditioning, ClassicalLearningPurkinje CellsRewardAnimalsMaleMiceOptogeneticscerebellar learningcerebellumclimbing fibercomplex spikePavlovian conditioningprediction errorPurkinje cellreinforcement learningreward learningrPE

Identifiers

PMID40848722
PMCPMC12380153

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.