Northwestern University Interdepartmental Neuroscience Program, and.
Department of Neurobiology, Northwestern University, Evanston, Illinois 60208.
J Neurosci. 2020 Apr 8;40(15):3063-3074. doi: 10.1523/JNEUROSCI.2322-19.2020. Epub 2020 Mar 5.
The cerebellum influences motor control through Purkinje target neurons, which transmit cerebellar output. Such output is required, for instance, for larval zebrafish to learn conditioned fictive swimming. The output cells, called eurydendroid neurons (ENs) in teleost fish, are inhibited by Purkinje cells and excited by parallel fibers. Here, we investigated the electrophysiological properties of glutamatergic ENs labeled by the transcription factor Action potential firing and synaptic responses were recorded in current clamp and voltage clamp from olig2 neurons in immobilized larval zebrafish (before sexual differentiation) and were correlated with motor behavior by simultaneous recording of fictive swimming. In the absence of swimming, olig2 ENs had basal firing rates near 8 spikes/s, and EPSCs and IPSCs were evident. Comparing Purkinje firing rates and eurydendroid IPSC rates indicated that 1-3 Purkinje cells converge onto each EN. Optogenetically suppressing Purkinje simple spikes, while preserving complex spikes, suggested that eurydendroid IPSC size depended on presynaptic spike duration rather than amplitude. During swimming, EPSC and IPSC rates increased. Total excitatory and inhibitory currents during sensory-evoked swimming were both more than double those during spontaneous swimming. During both spontaneous and sensory-evoked swimming, the total inhibitory current was more than threefold larger than the excitatory current. Firing rates of ENs nevertheless increased, suggesting that the relative timing of IPSCs and EPSCs may permit excitation to drive additional eurydendroid spikes. The data indicate that olig2 cells are ENs whose activity is modulated with locomotion, suiting them to participate in sensorimotor integration associated with cerebellum-dependent learning. The cerebellum contributes to movements through signals generated by cerebellar output neurons, called eurydendroid neurons (ENs) in fish (cerebellar nuclei in mammals). ENs receive sensory and motor signals from excitatory parallel fibers and inhibitory Purkinje cells. Here, we report electrophysiological recordings from ENs of larval zebrafish that directly illustrate how synaptic inhibition and excitation are integrated by cerebellar output neurons in association with motor behavior. The results demonstrate that inhibitory and excitatory drive both increase during fictive swimming, but inhibition greatly exceeds excitation. Firing rates nevertheless increase, providing evidence that synaptic integration promotes cerebellar output during locomotion. The data offer a basis for comparing aspects of cerebellar coding that are conserved and that diverge across vertebrates.
小脑通过浦肯野靶神经元影响运动控制,浦肯野靶神经元传递小脑输出。例如,这种输出对于幼虫斑马鱼学习条件性虚拟游泳是必需的。输出细胞在硬骨鱼中称为 eurydendroid 神经元(ENs),它们被浦肯野细胞抑制,被平行纤维兴奋。在这里,我们研究了标记转录因子 olig2 的谷氨酸能 ENs 的电生理特性。在固定的幼虫斑马鱼(在性分化之前)中,在电流钳和电压钳中记录动作电位放电和突触反应,并通过同时记录虚拟游泳来将其与运动行为相关联。在没有游泳的情况下,olig2 ENs 的基础放电率接近 8 个 spikes/s,并且存在 EPSC 和 IPSC。比较浦肯野细胞放电率和 eurydendroid IPSC 率表明,1-3 个浦肯野细胞会聚到每个 EN 上。光遗传学抑制浦肯野简单 spikes,同时保留复杂 spikes,表明 eurydendroid IPSC 大小取决于突触前 spike 持续时间而不是幅度。在游泳期间,EPSC 和 IPSC 率增加。感觉诱发游泳时的总兴奋性和抑制性电流均比自发游泳时高两倍以上。在自发游泳和感觉诱发游泳期间,总抑制性电流均比兴奋性电流大三倍以上。然而,ENs 的放电率增加,表明 IPSC 和 EPSC 的相对时间可能允许兴奋驱动额外的 eurydendroid spikes。数据表明,olig2 细胞是 ENs,其活性随运动而变化,适合参与与小脑依赖性学习相关的感觉运动整合。小脑通过称为 eurydendroid 神经元(ENs)的小脑输出神经元(在哺乳动物中称为小脑核)产生的信号来促进运动。ENs 接收来自兴奋性平行纤维和抑制性浦肯野细胞的感觉和运动信号。在这里,我们报告了来自幼虫斑马鱼 ENs 的电生理记录,这些记录直接说明了小脑输出神经元如何与运动行为相关联,整合突触抑制和兴奋。结果表明,在虚拟游泳期间,抑制性和兴奋性驱动均增加,但抑制性驱动大大超过兴奋性驱动。然而,放电率增加,这提供了证据表明突触整合促进了运动时的小脑输出。这些数据为比较脊椎动物中保守和发散的小脑编码方面提供了基础。