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分子层去抑制开启了小脑内攀缘纤维指导的运动学习。

Molecular layer disinhibition unlocks climbing-fiber-instructed motor learning in the cerebellum.

作者信息

Zhang Ke, Yang Zhen, Gaffield Michael A, Gross Garrett G, Arnold Don B, Christie Jason M

出版信息

bioRxiv. 2023 Aug 4:2023.08.04.552059. doi: 10.1101/2023.08.04.552059.

Abstract

Climbing fibers supervise cerebellar learning by providing signals to Purkinje cells (PCs) that instruct adaptive changes to mistakenly performed movements. Yet, climbing fibers are regularly active, even during well performed movements, suggesting that a mechanism dynamically regulates the ability of climbing fibers to induce corrective plasticity in response to motor errors. We found that molecular layer interneurons (MLIs), whose inhibition of PCs powerfully opposes climbing-fiber-mediated excitation, serve this function. Optogenetically suppressing the activity of floccular MLIs in mice during the vestibulo-ocular reflex (VOR) induces a learned increase in gain despite the absence of performance errors. Suppressing MLIs when the VOR is mistakenly underperformed reveled that their inhibitory output is necessary to orchestrate gain-increase learning by conditionally permitting climbing fibers to instruct plasticity induction during ipsiversive head turns. Ablation of an MLI circuit for PC disinhibition prevents gain-increase learning during VOR performance errors which was rescued by re-imposing PC disinhibition through MLI activity suppression. Our findings point to a decisive role for MLIs in gating climbing-fiber-mediated learning through their context-dependent inhibition of PCs.

摘要

攀缘纤维通过向浦肯野细胞(PCs)提供信号来监督小脑学习,这些信号指导对错误执行的运动进行适应性改变。然而,即使在运动执行良好时,攀缘纤维也会经常活跃,这表明存在一种机制动态调节攀缘纤维响应运动错误诱导纠正性可塑性的能力。我们发现,分子层中间神经元(MLIs),其对PCs的抑制有力地对抗攀缘纤维介导的兴奋,起到了这一作用。在小鼠前庭眼反射(VOR)期间,通过光遗传学抑制绒球MLIs的活动,尽管没有性能错误,也会诱导增益的学习性增加。当VOR错误执行时抑制MLIs发现,它们的抑制输出对于通过有条件地允许攀缘纤维在同侧头部转动期间指导可塑性诱导来协调增益增加学习是必要的。用于PC去抑制的MLI回路的消融会阻止VOR性能错误期间的增益增加学习,通过抑制MLI活动重新施加PC去抑制可挽救这种情况。我们的发现表明,MLIs通过其对PCs的上下文依赖性抑制在控制攀缘纤维介导的学习中起决定性作用。

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