Cell biology and dynamics of Neuronal Na+/K+-ATPase in health and diseases

Neuropharmacology. 2020 Jun 1:169:107461. doi: 10.1016/j.neuropharm.2018.12.008. Epub 2018 Dec 11.

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'.

Keywords: ATP1A3 disorders; Alzheimer's disease; Na(+)/K(+)-ATPase; Parkinson's disease; neurodegeneration.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Dystonic Disorders / diagnosis
  • Dystonic Disorders / enzymology
  • Dystonic Disorders / genetics
  • Hemiplegia / diagnosis
  • Hemiplegia / enzymology
  • Hemiplegia / genetics
  • Humans
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / genetics
  • Mental Disorders / diagnosis
  • Mental Disorders / enzymology*
  • Mental Disorders / genetics*
  • Mutation / genetics
  • Neurodegenerative Diseases / diagnosis
  • Neurodegenerative Diseases / enzymology*
  • Neurodegenerative Diseases / genetics*
  • Neurons / enzymology*
  • Neurons / pathology
  • Sodium-Potassium-Exchanging ATPase / biosynthesis*
  • Sodium-Potassium-Exchanging ATPase / genetics*

Substances

  • Membrane Proteins
  • Sodium-Potassium-Exchanging ATPase

Supplementary concepts

  • Alternating hemiplegia of childhood
  • Dystonia 12