Leibniz Institut für Alternsforschung-Fritz Lipmann Institut, 07743 Jena, Germany.
Institut für Humangenetik, Universitätsklinikum Jena, Friedrich-Schiller-Universität Jena, Germany.
Sci Rep. 2017 Jan 24;7:41248. doi: 10.1038/srep41248.
Rer1 is a sorting receptor in the early secretory pathway that controls the assembly and the cell surface transport of selected multimeric membrane protein complexes. Mice with a Purkinje cell (PC) specific deletion of Rer1 showed normal polarization and differentiation of PCs and normal development of the cerebellum. However, PC-specific loss of Rer1 led to age-dependent motor deficits in beam walk, ladder climbing and gait. Analysis of brain sections revealed a specific degeneration of PCs in the anterior cerebellar lobe in old animals. Electrophysiological recordings demonstrated severe deficits in spontaneous action potential generation. Measurements of resurgent currents indicated decreased surface densities of voltage-gated sodium channels (Na), but not changes in individual channels. Analysis of mice with a whole brain Rer1-deletion demonstrated a strong down-regulation of Na1.6 and 1.1 in the absence of Rer1, whereas protein levels of the related Ca2.1 and of K3.3 and 7.2 channels were not affected. The data suggest that Rer1 controls the assembly and transport of Na1.1 and 1.6, the principal sodium channels responsible for recurrent firing, in PCs.
Rer1 是早期分泌途径中的一种分拣受体,它控制着选定的多聚体膜蛋白复合物的组装和细胞表面转运。在浦肯野细胞(PC)中特异性缺失 Rer1 的小鼠表现出 PC 的极化和分化正常,小脑正常发育。然而,PC 特异性缺失 Rer1 导致在光束行走、爬梯和步态方面出现年龄依赖性的运动缺陷。对脑组织切片的分析显示,老年动物的前小脑叶中存在特定的 PC 退化。电生理记录显示自发性动作电位产生严重缺陷。复发性电流的测量表明,电压门控钠通道(Na)的表面密度降低,但单个通道没有变化。对全脑 Rer1 缺失的小鼠进行分析表明,在没有 Rer1 的情况下,Na1.6 和 1.1 的表达水平显著下调,而相关的 Ca2.1 以及 K3.3 和 7.2 通道的蛋白水平不受影响。数据表明,Rer1 控制着 Na1.1 和 1.6 的组装和运输,Na1.1 和 1.6 是负责复发性放电的主要钠通道,在 PC 中。