The PMCA pumps in genetically determined neuronal pathologies. (10th January 2018)

• Record Type: Journal Article
• Authors: Calì, Tito; Brini, Marisa; Carafoli, Ernesto
• Is Part Of: Neuroscience letters. Volume 663(2018)
• Page Start: 2
• Page End: 11
• Publication Date: 2018-01-10
• Subjects: Ca2+ signaling -- Plasma membrane calcium ATPases -- Deafness -- X-linked cerebellar ataxia -- Ca2+ microdomains; Neurology -- Periodicals; Neurology -- Periodicals; Research -- Periodicals; Neurologie -- Périodiques; Neuroanatomie -- Périodiques; Neuropharmacologie -- Périodiques; Neurophysiologie -- Périodiques; Neurology; Periodicals; Electronic journals; 617.48
• DOI: 10.1016/j.neulet.2017.11.005
• Languages: English
• ISSNs: 0304-3940

Abstract

Highlights: Plasma membrane Ca 2+ transporters are important for neuronal Ca 2+ signaling. Genetic mutations of PMCA pumps are associated with pathological phenotypes. Mutations of the neuron-specific PMCA2 and PMCA3 are linked to deafness and cerebellar ataxia, respectively. PMCA pumps are important in the local control of Ca 2+ in selected cell microdomains. Abstract: Ca 2+ signals regulate most aspects of animal cell life. They are of particular importance to the nervous system, in which they regulate specific functions, from neuronal development to synaptic plasticity. The homeostasis of cell Ca 2+ must thus be very precisely regulated: in all cells Ca 2+ pumps transport it from the cytosol to the extracellular medium (the Plasma Membrane Ca 2+ ATPases, hereafter referred to as PMCA pumps) or to the lumen of intracellular organelles (the Sarco/Endoplasmatic Reticulum Ca 2+ ATPase and the Secretory Pathway Ca 2+ ATPase, hereafter referred to as SERCA and SPCA pumps, respectively). In neurons and other excitable cells a powerful plasma membrane Na + /Ca 2+ exchanger (NCX) also exports Ca 2+ from cells. Quantitatively, the PMCA pumps are of minor importance to the bulk regulation of neuronal Ca 2+ . However, they are important in the regulation of Ca 2+ in specific sub-plasma membrane microdomains which contain a number of enzymes that are relevant to neuronal function. The PMCA pumps (of which 4 basic isoforms are expressed in animal cells) are P-type ATPases that are characterized by a long C-terminal cytosolic tail which is the site of interaction with most of the regulatory factors of the pump, the most important being calmodulin. In resting neurons, at low intracellular Ca 2+ the C-terminal tail of the PMCA interacts with the main body of the protein keeping it in an autoinhibited state. Local Ca 2+ increase activates calmodulin that removes the C-terminal tail from the inhibitory sites. Dysregulation of the Ca 2+ signals are incompatible with healthy neuronal life. A number of genetic mutations of PMCA pumps are associated with pathological phenotypes, those of the neuron-specific PMCA 2 and PMCA 3 being the best characterized. PMCA 2 mutations are associated with deafness and PMCA 3 mutations are linked to cerebellar ataxias. Biochemical analysis of the mutated pumps overexpressed in model cells have revealed their decreased ability to export Ca 2+ . The defect in the bulk cytosolic Ca 2+ homeostasis is minor, in keeping with the role of the PMCA pumps in the local control of Ca 2+ in specialized plasma membrane microdomains.