A view of SUR/KIR6.X, KATP channels

被引:465
作者
Babenko, AP
Aguilar-Bryan, L
Bryan, J
机构
[1] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
关键词
potassium channel; inward rectifier; sulfonylureas; KCO; ATP; ADP; ATPase; hyperinsulinism; cardioprotection;
D O I
10.1146/annurev.physiol.60.1.667
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
ATP-sensitive potassium channels, termed K-ATP channels, link the electrical activity of cell membranes to cellular metabolism. These channels are heteromultimers of sulfonylurea receptor (SUR) and K(IR)6.x subunits associated with a 1:1 stoichiometry as a tetramer (SUR/K(IR)6.x)(4). K(IR)6.x forms the pores, whereas SUR regulates their activity. Changes in [ATP](i) and [ADP](i) gate the channel. The diversity of K-ATP channels results from the assembly of SUR and K(IR)6.x subtypes. K(IR)6.1-based channels differ from K(IR)6.2 channels mainly by their smaller unitary conductance. SUR1- and SUR2-based channels are distinguished by their differential sensitivity to sulfonylureas, whereas SUR2A-based channels are distinguished from SUR2B channels by their differential sensitivity to diazoxide. Mutations that result in the loss of K-ATP channels in pancreatic beta-cells have been identified in SUR1 and K(IR)6.2. These mutations lead to familial hyperinsulinism. Understanding the mutations in SUR and K(IR)6.x is allowing insight into how these channels respond to nucleotides, sulfonylureas, and potassium channel openers, KCOs.
引用
收藏
页码:667 / 687
页数:21
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