CEA, Institut François Jacob (MIRcen) and CNRS, Laboratory of Neurodegenerative Diseases (U9199), 18 Route du Panorama, 92265, Fontenay-aux-Roses, France.
Institut de Biologie de l'ENS (IBENS), École Normale Supérieure, INSERM, CNRS, PSL, Research University, 46 Rue d'Ulm, 75005 Paris, France.
Neuropharmacology. 2020 Jun 1;169:107461. doi: 10.1016/j.neuropharm.2018.12.008. Epub 2018 Dec 11.
Neuronal Na/K-ATPase is responsible for the maintenance of ionic gradient across plasma membrane. In doing so, in a healthy brain, Na/K-ATPase activity accounts for nearly half of total brain energy consumption. The α3-subunit containing Na/K-ATPase expression is restricted to neurons. Heterozygous mutations within α3-subunit leads to Rapid-onset Dystonia Parkinsonism, Alternating Hemiplegia of Childhood and other neurological and neuropsychiatric disorders. Additionally, proteins such as α-synuclein, amyloid-β, tau and SOD1 whose aggregation is associated to neurodegenerative diseases directly bind and impair α3-Na/K-ATPase activity. The review will provide a summary of neuronal α3-Na/K-ATPase functional properties, expression pattern, protein-protein interactions at the plasma membrane, biophysical properties (distribution and lateral diffusion). Lastly, the role of α3-Na/K-ATPase in neurological and neurodegenerative disorders will be discussed. This article is part of the special issue entitled 'Mobility and trafficking of neuronal membrane proteins'.
神经元 Na/K-ATP 酶负责维持质膜两侧的离子梯度。在健康的大脑中,Na/K-ATP 酶的活性几乎占大脑总能量消耗的一半。含有α3 亚基的 Na/K-ATP 酶表达仅限于神经元。α3 亚基的杂合突变导致快速发作性运动障碍性帕金森病、儿童交替性偏瘫和其他神经和神经精神疾病。此外,与神经退行性疾病相关的聚集蛋白,如α-突触核蛋白、淀粉样β、tau 和 SOD1,直接结合并损害α3-Na/K-ATP 酶的活性。本综述将总结神经元α3-Na/K-ATP 酶的功能特性、表达模式、质膜上的蛋白-蛋白相互作用、生物物理特性(分布和侧向扩散)。最后,将讨论α3-Na/K-ATP 酶在神经和神经退行性疾病中的作用。本文是题为“神经元膜蛋白的流动性和运输”的特刊的一部分。