A-Kinase Anchoring Protein 9 and IKs Channel Regulation

被引:15
|
作者
Chen, Lei [1 ]
Kass, Robert S. [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Pharmacol, New York, NY 10032 USA
关键词
potassium channel; phosphorylation; long QT syndrome; AKAP; HEART POTASSIUM CHANNEL; LONG-QT SYNDROME; ADENYLYL-CYCLASE; SIGNALING COMPLEX; NMDA RECEPTOR; YOTIAO; PHYSIOLOGY; BINDING; CLONING; CENTROSOME;
D O I
10.1097/FJC.0b013e318232c80c
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A-kinase anchoring proteins AKAPs) create compartmentalized environment inside the cell to bring various signaling molecules to their targets. In the heart, a slowly activating potassium channel (I-Ks) important for cardiac repolarization is tightly regulated by the sympathetic nervous system in an AKAP-dependent manner. I-Ks channel forms a macromolecular complex with AKAP9 and other enzymes, such as protein kinase A, phosphatase, adenylyl cyclase, and phosphodiesterase, all of which are responsible to control the phosphorylation state of the channel. Such a complex thus ensures the I-Ks channel to be regulated properly to maintain the normal cardiac rhythm. Disruptions of various elements of the complex have been found to cause severe pathological consequences, including the long QT syndrome.
引用
收藏
页码:459 / 461
页数:3
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