CaMKII oxidative activation and the pathogenesis of cardiac disease

被引:128
作者
Luczak, Elizabeth D. [1 ,2 ]
Anderson, Mark E. [1 ,2 ,3 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Internal Med, Div Cardiovasc Med, Iowa City, IA USA
[2] Univ Iowa, Carver Coll Med, Cardiovasc Res Ctr, Iowa City, IA USA
[3] Univ Iowa, Carver Coll Med, Dept Mol Physiol & Biophys, Iowa City, IA USA
基金
美国国家卫生研究院;
关键词
Ca2+/calmodulin dependent protein kinase II; Reactive oxygen species; Heart failure; Arrhythmia; Calcium; Mitochondria; PROTEIN-KINASE-II; MYOCARDIAL-INFARCTION; SULFHYDRYL OXIDATION; INHIBITION PROTECTS; RYANODINE RECEPTOR; HEART-FAILURE; CALCIUM; STRESS; HYPERTROPHY; OXYGEN;
D O I
10.1016/j.yjmcc.2014.02.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Calcium and redox signaling both play important roles in the pathogenesis of cardiac disease; although how these signals are integrated in the heart remains unclear. One putative sensor for both calcium and oxidative stress in the heart is CaMKII, a calcium activated kinase that has recently been shown to also be regulated by oxidation. Oxidative activation of CaMKII occurs in several models of cardiac disease, including myocardial injury and inflammation, excessive neurohumoral activation, atrial fibrillation, and sinus node dysfunction. Additionally, oxidative activation of CaMKII is suggested in subcellular domains where calcium and ROS signaling intersect, such as mitochondria. This review describes the mechanism of activation of CaMKII by oxidation, the cardiac diseases where oxidized CaMKII has been identified, and suggests contexts where oxidized CaMKII is likely to play an important role. This article is part of a Special Issue entitled "Redox Signalling in the Cardiovascular System". (c) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:112 / 116
页数:5
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