A cerebellar granule cell-climbing fiber computation to learn to track long time intervals

被引:3
|
作者
Garcia-Garcia, Martha G. [1 ]
Kapoor, Akash [1 ]
Akinwale, Oluwatobi [1 ]
Takemaru, Lina [1 ]
Kim, Tony Hyun [2 ]
Paton, Casey [1 ]
Litwin-Kumar, Ashok [3 ]
Schnitzer, Mark J. [4 ]
Luo, Liqun [2 ]
Wagner, Mark J. [1 ]
机构
[1] Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD 20894 USA
[2] Stanford Univ, Howard Hughes Med Inst, Dept Biol, Stanford, CA 94305 USA
[3] Columbia Univ, Zuckerman Mind Brain Behav Inst, Dept Neurosci, New York, NY 10027 USA
[4] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
关键词
PREFRONTAL CORTEX; NEURAL CIRCUIT; PLASTICITY; MECHANISM; REPRESENTATION; CONSEQUENCES; ACTIVATION; DEPRESSION; EXPRESSION; PREDICTION;
D O I
10.1016/j.neuron.2024.05.019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In classical cerebellar learning, Purkinje cells (PkCs) associate climbing fiber (CF) error signals with predictive granule cells (GrCs) that were active just prior ( 150 ms). The cerebellum also contributes to behaviors characterized by longer timescales. To investigate how GrC-CF-PkC circuits might learn seconds-long predictions, we imaged simultaneous GrC-CF activity over days of forelimb operant conditioning for delayed water reward. As mice learned reward timing, numerous GrCs developed anticipatory activity ramping at different rates until reward delivery, followed by widespread time-locked CF spiking. Relearning longer delays further lengthened GrC activations. We computed CF-dependent GrC-PkC plasticity rules, demonstrating that reward-evoked CF spikes sufficed to grade many GrC synapses by anticipatory timing. We predicted and confirmed that PkCs could thereby continuously ramp across seconds-long intervals from movement to reward. Learning thus leads to new GrC temporal bases linking predictors to remote CF reward signals-a strategy well suited for learning to track the long intervals common in cognitive domains.
引用
收藏
页数:24
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