ATP-sensitive potassium channels: A model of heteromultimeric potassium channel/receptor assemblies

被引:414
作者
Seino, S [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Mol Med, Chuo Ku, Chiba 2608670, Japan
关键词
inward rectifiers; sulfonylurea receptors; ATP-binding cassette protein superfamily; ADP; glibenclamide;
D O I
10.1146/annurev.physiol.61.1.337
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
ATP-sensitive K+ channels (K-ATP channels) play important roles in many cellular functions by coupling cell metabolism to electrical activity. By cloning members of the novel inwardly rectifying K+ channel subfamily Kir6.0 (Kir6.1 and Kir6.2) and the receptors for sulfonylureas (SUR1 and SUR2), researchers have clarified the molecular structure of K-ATP channels. K-ATP channels comprise two subunits: a Kir6.0 subfamily subunit, which is a member of the inwardly rectifying K+ channel family; and a SUR subunit, which is a member of the ATP-binding cassette (ABC) protein superfamily. K-ATP channels are the first example of a heteromultimeric complex assembled with a K+ channel and a receptor that are structurally unrelated to each other. Since 1995, molecular biological and molecular genetic studies of K-ATP channels have provided insights into the structure-function relationships, molecular regulation, and pathophysiological roles of K-ATP channels.
引用
收藏
页码:337 / 362
页数:26
相关论文
共 137 条
[81]   Independent trafficking of KATP channel subunits to the plasma membrane [J].
Makhina, EN ;
Nichols, CG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (06) :3369-3374
[82]   Molecular site for nucleotide binding on an ATP-sensitive renal K+ channel (ROMK2) [J].
McNicholas, CM ;
Yang, YH ;
Giebisch, G ;
Hebert, SC .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1996, 271 (02) :F275-F285
[83]   Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator [J].
McNicholas, CM ;
Guggino, WB ;
Schwiebert, EM ;
Hebert, SC ;
Giebisch, G ;
Egan, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :8083-8088
[84]   Abnormalities of pancreatic islets by targeted expression of a dominant-negative K-ATP channel [J].
Miki, T ;
Tashiro, F ;
Iwanaga, T ;
Nagashima, K ;
Yoshitomi, H ;
Aihara, H ;
Nitta, Y ;
Gonoi, T ;
Inagaki, N ;
Miyazaki, J ;
Seino, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (22) :11969-11973
[85]   Defective insulin secretion and enhanced insulin action in KATP channel-deficient mice [J].
Miki, T ;
Nagashima, K ;
Tashiro, F ;
Kotake, K ;
Yoshitomi, H ;
Tamamoto, A ;
Gonoi, T ;
Iwanaga, T ;
Miyazaki, J ;
Seino, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10402-10406
[86]  
Misler S, 1992, Curr Opin Nephrol Hypertens, V1, P21, DOI 10.1097/00041552-199210000-00005
[87]  
NELSON DA, 1992, J BIOL CHEM, V267, P14928
[88]   Mutations in the sulfonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews [J].
Nestorowicz, A ;
Wilson, BA ;
Schoor, KP ;
Inoue, H ;
Glaser, B ;
Landau, H ;
Stanley, CA ;
Thornton, PS ;
Clement, JP ;
Bryan, J ;
AguilarBryan, L ;
Permutt, MA .
HUMAN MOLECULAR GENETICS, 1996, 5 (11) :1813-1822
[89]   A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism [J].
Nestorowicz, A ;
Inagaki, N ;
Gonoi, T ;
Schoor, KP ;
Wilson, BA ;
Glaser, B ;
Landau, H ;
Stanley, CA ;
Thornton, PS ;
Seino, S ;
Permutt, MA .
DIABETES, 1997, 46 (11) :1743-1748
[90]   Adenosine diphosphate as an intracellular regulator of insulin secretion [J].
Nichols, CG ;
Shyng, SL ;
Nestorowicz, A ;
Glaser, B ;
Clement, JP ;
Gonzalez, G ;
AguilarBryan, L ;
Permutt, MA ;
Bryan, J .
SCIENCE, 1996, 272 (5269) :1785-1787