Mitochondrial Sirtuins and Molecular Mechanisms of Aging

被引:252
作者
van de Ven, Robert A. H. [1 ]
Santos, Daniel [1 ,2 ]
Haigis, Marcia C. [1 ]
机构
[1] Harvard Med Sch, Dept Cell Biol, Boston, MA 02115 USA
[2] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, P-3004504 Coimbra, Portugal
关键词
FATTY-ACID OXIDATION; DNA-DAMAGE RESPONSE; CALORIE RESTRICTION; SKELETAL-MUSCLE; SIRT3-MEDIATED DEACETYLATION; NICOTINAMIDE MONONUCLEOTIDE; SIRT3; DEACETYLATES; MNSOD ACTIVITY; BALANCING ACT; NAD(+);
D O I
10.1016/j.molmed.2017.02.005
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
Advancing age is the major risk factor for the development of chronic diseases and is accompanied by changes in metabolic processes and mitochondrial dysfunction. Mitochondrial sirtuins (SIRT3-5) are part of the sirtuin family of NAD(+)-dependent deacylases and ADP-ribosyl transferases. The dependence on NAD(+) links sirtuin enzymatic activity to the metabolic state of the cell, poising them as stress sensors. Recent insights have revealed that SIRT3-5 orchestrate stress responses through coordinated regulation of substrate clusters rather than of a few key metabolic enzymes. Additionally, mitochondrial sirtuin function has been implicated in the protection against age-related pathologies, including neurodegeneration, cardiopathologies, and insulin resistance. In this review, we highlight the molecular targets of SIRT3-5 and discuss their involvement in aging and age-related pathologies.
引用
收藏
页码:320 / 331
页数:12
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