Evidence for a role of plasma membrane calcium pumps in neurodegenerative disease: Recent developments

Abstract

Plasma membrane Ca²⁺ ATPases (PMCAs) are a major system for calcium extrusion from all cells. Different PMCA isoforms and splice variants are involved in the precise temporal and spatial handling of Ca²⁺ signals and the re-establishment of resting Ca²⁺ levels in the nervous system. Lack or inappropriate expression of specific PMCAs leads to characteristic neuronal phenotypes, which may be reciprocally exacerbated by genetic predisposition through alleles in other genes that modify PMCA interactions, regulation, and function. PMCA dysfunction is often poorly compensated in neurons and may lead to changes in synaptic transmission, altered excitability and, with long-term calcium overload, eventual cell death. Decrease and functional decline of PMCAs are hallmarks of neurodegeneration during aging, and mutations in specific PMCAs are responsible for neuronal dysfunction and accelerated neurodegeneration in many sensory and cognitive diseases.

Keywords: Calcium homeostasis; Cerebellar ataxia; Excitotoxicity; Neurodegenerative disease; Plasma membrane calcium ATPase.