Roles of glial ion transporters in brain diseases.
Shanshan SongLanxin LuoBaoshan SunDandan SunPublished in: Glia (2019)
Glial ion transporters are important in regulation of ionic homeostasis, cell volume, and cellular signal transduction under physiological conditions of the central nervous system (CNS). In response to acute or chronic brain injuries, these ion transporters can be activated and differentially regulate glial functions, which has subsequent impact on brain injury or tissue repair and functional recovery. In this review, we summarized the current knowledge about major glial ion transporters, including Na+ /H+ exchangers (NHE), Na+ /Ca2+ exchangers (NCX), Na+ -K+ -Cl- cotransporters (NKCC), and Na+ -HCO3 - cotransporters (NBC). In acute neurological diseases, such as ischemic stroke and traumatic brain injury (TBI), these ion transporters are rapidly activated and play significant roles in regulation of the intra- and extracellular pH, Na+ , K+ , and Ca2+ homeostasis, synaptic plasticity, and myelin formation. However, overstimulation of these ion transporters can contribute to glial apoptosis, demyelination, inflammation, and excitotoxicity. In chronic brain diseases, such as glioma, Alzheimer's disease (AD), Parkinson's disease (PD), and multiple sclerosis (MS), glial ion transporters are involved in the glioma Warburg effect, glial activation, neuroinflammation, and neuronal damages. These findings suggest that glial ion transporters are involved in tissue structural and functional restoration, or brain injury and neurological disease development and progression. A better understanding of these ion transporters in acute and chronic neurological diseases will provide insights for their potential as therapeutic targets.
Keyphrases
- brain injury
- cerebral ischemia
- traumatic brain injury
- multiple sclerosis
- neuropathic pain
- subarachnoid hemorrhage
- liver failure
- white matter
- oxidative stress
- healthcare
- drug induced
- stem cells
- resting state
- spinal cord injury
- aortic dissection
- protein kinase
- atrial fibrillation
- cell therapy
- cognitive decline
- inflammatory response
- lps induced
- functional connectivity
- ms ms
- lipopolysaccharide induced
- hepatitis b virus