CaMKII as a Therapeutic Target in Cardiovascular Disease

被引:65
作者
Gaido, Oscar E. Reyes [1 ]
Nkashama, Lubika J. [2 ]
Schole, Kate L. [1 ]
Wang, Qinchuan [1 ]
Umapathi, Priya [1 ]
Mesubi, Olurotimi O. [1 ]
Konstantinidis, Klitos [1 ]
Luczak, Elizabeth D. [1 ]
Anderson, Mark E. [1 ,3 ,4 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Cleveland Clin, Lerner Coll Med, Cleveland, OH USA
[3] Johns Hopkins Univ, Sch Med, Dept Physiol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Med Genet, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Program Cellular & Mol Med, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
CaMKII; cardiovascular disease; kinase; calcium; heart failure; arrhythmias; PROTEIN-KINASE-II; RETICULUM CA2+ LEAK; RYANODINE RECEPTOR PHOSPHORYLATION; NF-KAPPA-B; CARDIAC-HYPERTROPHY; MYOCARDIAL ISCHEMIA/REPERFUSION; AUTOPHOSPHORYLATION SITES; SYNAPTIC PLASTICITY; INHIBITION PROTECTS; HEART-FAILURE;
D O I
10.1146/annurev-pharmtox-051421-111814
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CaMKII (the multifunctional Ca2+ and calmodulin-dependent protein kinase II) is a highly validated signal for promoting a variety of common diseases, particularly in the cardiovascular system. Despite substantial amounts of convincing preclinical data, CaMKII inhibitors have yet to emerge in clinical practice. Therapeutic inhibition is challenged by the diversity of CaMKII isoforms and splice variants and by physiological CaMKII activity that contributes to learning and memory. Thus, uncoupling the harmful and beneficial aspects of CaMKII will be paramount to developing effective therapies. In the last decade, several targeting strategies have emerged, including small molecules, peptides, and nucleotides, which hold promise in discriminating pathological from physiological CaMKII activity. Here we review the cellular and molecular biology of CaMKII, discuss its role in physiological and pathological signaling, and consider new findings and approaches for developing CaMKII therapeutics.
引用
收藏
页码:249 / 272
页数:24
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