Department of Neuroscience, Erasmus MC, 3000 DR Rotterdam, the Netherlands.
Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, VU University Amsterdam, 1081 HV Amsterdam, the Netherlands.
Cell Rep. 2020 Apr 14;31(2):107515. doi: 10.1016/j.celrep.2020.03.079.
The majority of excitatory postsynaptic currents in the brain are gated through AMPA-type glutamate receptors, the kinetics and trafficking of which can be modulated by auxiliary proteins. It remains to be elucidated whether and how auxiliary proteins can modulate synaptic function to contribute to procedural memory formation. In this study, we report that the AMPA-type glutamate receptor (AMPAR) auxiliary protein SHISA6 (CKAMP52) is expressed in cerebellar Purkinje cells, where it co-localizes with GluA2-containing AMPARs. The absence of SHISA6 in Purkinje cells results in severe impairments in the adaptation of the vestibulo-ocular reflex and eyeblink conditioning. The physiological abnormalities include decreased presence of AMPARs in synaptosomes, impaired excitatory transmission, increased deactivation of AMPA receptors, and reduced induction of long-term potentiation at Purkinje cell synapses. Our data indicate that Purkinje cells require SHISA6-dependent modification of AMPAR function in order to facilitate cerebellar, procedural memory formation.
大脑中大多数兴奋性突触后电流通过 AMPA 型谷氨酸受体门控,其动力学和运输可被辅助蛋白调节。目前尚不清楚辅助蛋白是否以及如何调节突触功能以促进程序记忆的形成。在这项研究中,我们报告说,AMPA 型谷氨酸受体 (AMPAR) 辅助蛋白 SHISA6 (CKAMP52) 在小脑浦肯野细胞中表达,在那里它与包含 GluA2 的 AMPAR 共定位。浦肯野细胞中 SHISA6 的缺失导致前庭眼反射和眨眼条件反射的适应严重受损。生理异常包括突触小体中 AMPAR 的存在减少、兴奋性传递受损、AMPA 受体去活增加以及浦肯野细胞突触长时程增强的诱导减少。我们的数据表明,浦肯野细胞需要 SHISA6 依赖性的 AMPAR 功能修饰,以促进小脑程序性记忆的形成。