Cerebellar climbing fibers impact experience-dependent plasticity in the mouse primary somatosensory cortex

In the cerebellum, climbing fibers (CFs) provide instructive signals for supervised learning at parallel fiber to Purkinje cell synapses. It has not been tested so far whether CF signaling may also influence plasticity in other brain areas. Here, we show that optogenetic CF activation suppresses potentiation of whisker responses in layer 2/3 pyramidal cells in the primary somatosensory (S1) cortex of awake mice that is observed after repeated whisker stimulation. Using two-photon imaging and chemogenetics, we find that CFs control plasticity by modulating SST- and VIP-positive interneurons in S1 cortex. Transsynaptic labeling identifies zona incerta (ZI) to thalamic posterior medial nucleus projections as a pathway for cerebellar output reaching S1 cortex. Chemogenetic inhibition of PV-positive neurons in the ZI prevents CF co-activation effects, identifying the ZI as a critical relay. Our findings demonstrate that CFs impact sensory signal processing and plasticity in S1 cortex and thus may convey instructive signals.

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Publication Details

Journal
eLife
Published
2025-10-24
DOI
https://doi.org/10.7554/elife.109183
Citations
1
Primary Topic
Vestibular and auditory disorders
Type
article
Field-Weighted Citation Impact
0.84

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article

Cerebellar climbing fibers impact experience-dependent plasticity in the mouse primary somatosensory cortex

Christian Hansel, Kevin P. Koster, Abby Silbaugh
1 citations
eLife
Vestibular and auditory disorders
0.84
article

Cerebellar climbing fibers impact experience-dependent plasticity in the mouse primary somatosensory cortex

Christian Hansel, Kevin P. Koster, Abby Silbaugh
article en
1 citations

Abstract

In the cerebellum, climbing fibers (CFs) provide instructive signals for supervised learning at parallel fiber to Purkinje cell synapses. It has not been tested so far whether CF signaling may also influence plasticity in other brain areas. Here, we show that optogenetic CF activation suppresses potentiation of whisker responses in layer 2/3 pyramidal cells in the primary somatosensory (S1) cortex of awake mice that is observed after repeated whisker stimulation. Using two-photon imaging and chemogenetics, we find that CFs control plasticity by modulating SST- and VIP-positive interneurons in S1 cortex. Transsynaptic labeling identifies zona incerta (ZI) to thalamic posterior medial nucleus projections as a pathway for cerebellar output reaching S1 cortex. Chemogenetic inhibition of PV-positive neurons in the ZI prevents CF co-activation effects, identifying the ZI as a critical relay. Our findings demonstrate that CFs impact sensory signal processing and plasticity in S1 cortex and thus may convey instructive signals.

eLifeVol. 14
University of Chicago (US), Neuroscience Institute (IT)
National Institutes of Health, National Institute of Neurological Disorders and Stroke
Openalex Percentile: Top 20%
Vestibular and auditory disorders
0.84
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Cerebellar climbing fibers impact experience-dependent plasticity in the mouse primary somatosensory cortex — Christian Hansel, Kevin P. Koster, et al. · eLife (2025) | TGRS Research Map | TGRS