Mitochondrial Sirtuins in cardiometabolic diseases

被引:77
作者
Tang, Xiaoqiang
Chen, Xiao-Feng
Chen, Hou-Zao [1 ]
Liu, De-Pei [1 ]
机构
[1] Chinese Acad Med Sci, State Key Lab Med Mol Biol, Dept Biochem & Mol Biol, Inst Basic Med Sci, 5 Dong Dan San Tiao, Beijing 100005, Peoples R China
基金
中国国家自然科学基金;
关键词
FATTY-ACID OXIDATION; ISCHEMIA-REPERFUSION; CARDIOVASCULAR-DISEASE; CALORIE RESTRICTION; SIRT3; DEACETYLATES; ENDOTHELIAL-CELLS; ANTIOXIDANT SUPPLEMENTS; HEART-FAILURE; SIRT3-MEDIATED DEACETYLATION; MICROVASCULAR DYSFUNCTION;
D O I
10.1042/CS20160685
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mitochondria are heterogeneous and essentially contribute to cellular functions and tissue homeostasis. Mitochondrial dysfunction compromises overall cell functioning, tissue damage, and diseases. The advances in mitochondrion biology increase our understanding of mitochondrial dynamics, bioenergetics, and redox homeostasis, and subsequently, their functions in tissue homeostasis and diseases, including cardiometabolic diseases (CMDs). The functions of mitochondria mainly rely on the enzymes in theirmatrix. Sirtuins are a family of NAD(+)-dependent deacylases and ADP-ribosyltransferases. Three members of the Sirtuin family (SIRT3, SIRT4, and SIRT5) are located in the mitochondrion. These mitochondrial Sirtuins regulate energy and redox metabolism as well as mitochondrial dynamics in the mitochondrial matrix and are involved in cardiovascular homeostasis and CMDs. In this review, we discuss the advances in our understanding of mitochondrial Sirtuins in mitochondrion biology and CMDs, including cardiac remodeling, pulmonary artery hypertension, and vascular dysfunction. The potential therapeutic strategies by targetting mitochondrial Sirtuins to improve mitochondrial function in CMDs are also addressed.
引用
收藏
页码:2063 / 2078
页数:16
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