Acid-Sensing Ion Channel 2: Function and Modulation

被引:10
作者
Sivils, Andy [1 ]
Yang, Felix [1 ]
Wang, John Q. [1 ]
Chu, Xiang-Ping [1 ]
机构
[1] Univ Missouri, Sch Med, Dept Biomed Sci, Kansas City, MO 64108 USA
关键词
acid-sensing ion channels; ASIC2; function; physiology; pathology; pharmacology; modulation; DORSAL-ROOT GANGLIA; SYNAPTIC PLASTICITY; HUNTINGTONS-DISEASE; SENSITIVE CHANNELS; EXTRACELLULAR PH; SENSORY NEURONS; NMDA RECEPTOR; UP-REGULATION; MOUSE MODEL; ASIC2;
D O I
10.3390/membranes12020113
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acid-sensing ion channels (ASICs) have an important influence on human physiology and pathology. They are members of the degenerin/epithelial sodium channel family. Four genes encode at least six subunits, which combine to form a variety of homotrimers and heterotrimers. Of these, ASIC1a homotrimers and ASIC1a/2 heterotrimers are most widely expressed in the central nervous system (CNS). Investigations into the function of ASIC1a in the CNS have revealed a wealth of information, culminating in multiple contemporary reviews. The lesser-studied ASIC2 subunits are in need of examination. This review will focus on ASIC2 in health and disease, with discussions of its role in modulating ASIC function, synaptic targeting, cardiovascular responses, and pharmacology, while exploring evidence of its influence in pathologies such as ischemic brain injury, multiple sclerosis, epilepsy, migraines, drug addiction, etc. This information substantiates the ASIC2 protein as a potential therapeutic target for various neurological, psychological, and cerebrovascular diseases.
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页数:21
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