Department of Neuroscience, Erasmus Medical Center, Rotterdam, Netherlands.
Department of Translational Neuroscience, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Elife. 2019 Sep 5;8:e45590. doi: 10.7554/eLife.45590.
Despite the canonical homogeneous character of its organization, the cerebellum plays differential computational roles in distinct sensorimotor behaviors. Previously, we showed that Purkinje cell (PC) activity differs between zebrin-negative (Z-) and zebrin-positive (Z+) modules (Zhou et al., 2014). Here, using gain-of-function and loss-of-function mouse models, we show that transient receptor potential cation channel C3 (TRPC3) controls the simple spike activity of Z-, but not Z+ PCs. In addition, TRPC3 regulates complex spike rate and their interaction with simple spikes, exclusively in Z- PCs. At the behavioral level, TRPC3 loss-of-function mice show impaired eyeblink conditioning, which is related to Z- modules, whereas compensatory eye movement adaptation, linked to Z+ modules, is intact. Together, our results indicate that TRPC3 is a major contributor to the cellular heterogeneity that introduces distinct physiological properties in PCs, conjuring functional heterogeneity in cerebellar sensorimotor integration.
尽管小脑组织在结构上具有典型的均一性,但它在不同的感觉运动行为中发挥着不同的计算作用。此前,我们发现浦肯野细胞(PC)在阴性斑马带(Z-)和阳性斑马带(Z+)区域的活动存在差异(Zhou 等人,2014)。在这里,我们使用功能获得和功能丧失的小鼠模型表明,瞬时受体电位阳离子通道 C3(TRPC3)控制 Z-区域而非 Z+区域 PC 的简单峰活动。此外,TRPC3 调节复杂峰频率及其与简单峰的相互作用,仅在 Z-区域 PC 中发生。在行为水平上,TRPC3 功能丧失型小鼠表现出眨眼条件反射受损,这与 Z-区域模块有关,而与 Z+区域模块相关的代偿性眼球运动适应则保持完整。总之,我们的结果表明,TRPC3 是引入 PC 中不同生理特性的细胞异质性的主要贡献者,为小脑感觉运动整合带来了功能异质性。