Molecular identification and functional roles of a Ca2+-activated K+ channel in human and mouse hearts

被引:227
作者
Xu, YF
Tuteja, D
Zhang, Z
Xu, DY
Zhang, Y
Rodriguez, J
Nie, LP
Tuxson, HR
Young, JN
Glatter, KA
Vázquez, AE
Yamoah, EN
Chiamvimonvat, N
机构
[1] Univ Calif Davis, Dept Internal Med, Div Cardiovasc Med, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Cardiothorac Surg, Davis, CA 95616 USA
[3] Univ Calif Davis, Ctr Neurosci, Dept Otolaryngol, Davis, CA 95616 USA
[4] No Calif Hlth Care Syst, Dept Vet Affairs, Mather, CA 95655 USA
[5] Hebei Med Univ, Dept Pharmacol, Shijiazhuang 050017, Peoples R China
关键词
D O I
10.1074/jbc.M307508200
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
The repolarization phase of cardiac action potential is prone to aberrant excitation that is common in cardiac patients. Here, we demonstrate that this phase is markedly sensitive to Ca2+ because of the surprising existence of a Ca2+-activated K+ currents in cardiac cells. The current was revealed using recording conditions that preserved endogenous Ca2+ buffers. The Ca2+-activated K+ current is expressed differentially in atria compared with ventricles. Because of the significant contribution of the current toward membrane repolarization in cardiac myocytes, alterations of the current magnitude precipitate abnormal action potential profiles. We confirmed the presence of a small conductance Ca2+-activated K+ channel subtype (SK2) in human and mouse cardiac myocytes using Western blot analysis and reverse transcription-polymerase chain reaction and have cloned SK2 channels from human atria, mouse atria, and ventricles. Because of the marked differential expression of SK2 channels in the heart, specific ligands for Ca2+-activated K+ currents may offer a unique therapeutic opportunity to modify atrial cells without interfering with ventricular myocytes.
引用
收藏
页码:49085 / 49094
页数:10
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