Regulation of AQP4 in the Central Nervous System

被引:153
作者
Vandebroek, Arno [1 ]
Yasui, Masato [1 ]
机构
[1] Keio Univ, Sch Med, Dept Pharmacol, Shinjuku Ku, 35 Shinanomachi, Tokyo 1608582, Japan
基金
日本学术振兴会;
关键词
aquaporin-4; phosphorylation; microRNA; metal ion; water channel; small molecule inhibitor; TGN-020; acetazolamide; oocyte; proteoliposome; ATTENUATES BRAIN EDEMA; PROTEIN-KINASE-C; AQUAPORIN; 4; WATER-CHANNEL; INTRACEREBRAL HEMORRHAGE; THERAPEUTIC TARGET; CRYSTAL-STRUCTURE; TRANSGENIC MICE; DOWN-REGULATION; UP-REGULATION;
D O I
10.3390/ijms21051603
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
Aquaporin-4 (AQP4) is the main water channel protein expressed in the central nervous system (CNS). AQP4 is densely expressed in astrocyte end-feet, and is an important factor in CNS water and potassium homeostasis. Changes in AQP4 activity and expression have been implicated in several CNS disorders, including (but not limited to) epilepsy, edema, stroke, and glioblastoma. For this reason, many studies have been done to understand the various ways in which AQP4 is regulated endogenously, and could be regulated pharmaceutically. In particular, four regulatory methods have been thoroughly studied; regulation of gene expression via microRNAs, regulation of AQP4 channel gating/trafficking via phosphorylation, regulation of water permeability using heavy metal ions, and regulation of water permeability using small molecule inhibitors. A major challenge when studying AQP4 regulation is inter-method variability. A compound or phosphorylation which shows an inhibitory effect in vitro may show no effect in a different in vitro method, or even show an increase in AQP4 expression in vivo. Although a large amount of variability exists between in vitro methods, some microRNAs, heavy metal ions, and two small molecule inhibitors, acetazolamide and TGN-020, have shown promise in the field of AQP4 regulation.
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页数:16
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