| Literature DB >> 30550795 |
Amulya Nidhi Shrivastava1, Antoine Triller2, Ronald Melki3.
Abstract
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'.Entities:
Keywords: ATP1A3 disorders; Alzheimer's disease; Na(+)/K(+)-ATPase; Parkinson's disease; neurodegeneration
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Year: 2018 PMID: 30550795 DOI: 10.1016/j.neuropharm.2018.12.008
Source DB: PubMed Journal: Neuropharmacology ISSN: 0028-3908 Impact factor: 5.250