CD38: A Potential Therapeutic Target in Cardiovascular Disease

被引:15
作者
Zuo, Wanyun [1 ]
Liu, Na [1 ]
Zeng, Yunhong [2 ]
Liu, Yaozhong [1 ]
Li, Biao [1 ]
Wu, Keke [1 ]
Xiao, Yunbin [2 ]
Liu, Qiming [1 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Cardiovasc Med, 139 Middle Renmin Rd, Changsha 410011, Hunan, Peoples R China
[2] Hunan Childrens Hosp, Dept Cardiol, 86 Ziyuan Rd, Changsha 410007, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
CD38; NAD plus; cADPR; Calcium regulation; Sirtuins; Cardiovascular diseases; CYCLIC ADP-RIBOSE; ATRIAL-FIBRILLATION; CA2+ RELEASE; MITOCHONDRIAL DYSFUNCTION; ENDOTHELIAL DYSFUNCTION; INTRACELLULAR CALCIUM; NAD(+) METABOLISM; OXIDATIVE STRESS; CELLULAR NAD; GENE FAMILY;
D O I
10.1007/s10557-020-07007-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Substantial research has demonstrated the association between cardiovascular disease and the dysregulation of intracellular calcium, ageing, reduction in nicotinamide adenine dinucleotide NAD+ content, and decrease in sirtuin activity. CD38, which comprises the soluble type, type II, and type III, is the main NADase in mammals. This molecule catalyses the production of cyclic adenosine diphosphate ribose (cADPR), nicotinic acid adenine dinucleotide phosphate (NAADP), and adenosine diphosphate ribose (ADPR), which stimulate the release of Ca2+, accompanied by NAD+ consumption and decreased sirtuin activity. Therefore, the relationship between cardiovascular disease and CD38 has been attracting increased attention. In this review, we summarize the structure, regulation, function, targeted drug development, and current research on CD38 in the cardiac context. More importantly, we provide original views about the as yet elusive mechanisms of CD38 action in certain cardiovascular disease models. Based on our review, we predict that CD38 may serve as a novel therapeutic target in cardiovascular disease in the future.
引用
收藏
页码:815 / 828
页数:14
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