Department of Anatomy and Physiology, The University of Melbourne, Parkville, Victoria, 3010, Australia.
German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Mol Neurobiol. 2022 Feb;59(2):1183-1198. doi: 10.1007/s12035-021-02660-y. Epub 2021 Dec 27.
The membrane protein seizure 6-like (SEZ6L) is a neuronal substrate of the Alzheimer's disease protease BACE1, and little is known about its physiological function in the nervous system. Here, we show that SEZ6L constitutive knockout mice display motor phenotypes in adulthood, including changes in gait and decreased motor coordination. Additionally, SEZ6L knockout mice displayed increased anxiety-like behaviour, although spatial learning and memory in the Morris water maze were normal. Analysis of the gross anatomy and proteome of the adult SEZ6L knockout cerebellum did not reveal any major differences compared to wild type, indicating that lack of SEZ6L in other regions of the nervous system may contribute to the phenotypes observed. In summary, our study establishes physiological functions for SEZ6L in regulating motor coordination and curbing anxiety-related behaviour, indicating that aberrant SEZ6L function in the human nervous system may contribute to movement disorders and neuropsychiatric diseases.
膜蛋白发作 6 样(SEZ6L)是阿尔茨海默病蛋白酶 BACE1 的神经元底物,其在神经系统中的生理功能知之甚少。在这里,我们表明 SEZ6L 组成型敲除小鼠在成年期表现出运动表型,包括步态变化和运动协调能力下降。此外,SEZ6L 敲除小鼠表现出焦虑样行为增加,尽管在 Morris 水迷宫中的空间学习和记忆正常。与野生型相比,对成年 SEZ6L 敲除小脑的大体解剖和蛋白质组分析并未显示出任何重大差异,这表明缺乏 SEZ6L 在神经系统的其他区域可能导致观察到的表型。总之,我们的研究确立了 SEZ6L 在调节运动协调和抑制焦虑相关行为中的生理功能,表明人类神经系统中异常的 SEZ6L 功能可能导致运动障碍和神经精神疾病。