A comprehensive review of Sirtuins: With a major focus on redox homeostasis and metabolism

被引:77
作者
Shahgaldi, Shahab [1 ]
Kahmini, Fatemeh Rezaei [2 ]
机构
[1] Tarbiat Modares Univ, Fac Med Sci, Dept Immunol, POB 14115-331, Tehran, Iran
[2] Shiraz Univ Med Sci, Autoimmune Dis Res Ctr, Shiraz, Iran
关键词
Sirtuins; Metabolism; Oxidative stress; Antioxidant defense; Post-translational modification; Transcriptional regulation; FATTY-ACID OXIDATION; PROMOTES CELL-SURVIVAL; PYRUVATE-KINASE M2; MITOCHONDRIAL-FUNCTION; GLUCOSE-METABOLISM; SIRT3-MEDIATED DEACETYLATION; SIRT5; DESUCCINYLATES; ENERGY-EXPENDITURE; ACETYLATION STATUS; LIPID-METABOLISM;
D O I
10.1016/j.lfs.2021.119803
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Sirtuins are Class III protein deacetylases with seven conserved isoforms. In general, Sirtuins are highly activated under cellular stress conditions in which NAD+ levels are increased. Nevertheless, regulation of Sirtuins extends far beyond the influences of cellular NAD+/NADH ratio and a rapidly expanding body of evidence currently suggests that their expression and catalytic activity are highly kept under control at multiple levels by various factors and processes. Owing to their intrinsic ability to enzymatically target various intracellular proteins, Sirtuins are prominently involved in the regulation of fundamental biological processes including inflammation, metabolism, redox homeostasis, DNA repair and cell proliferation and senescence. In fact, Sirtuins are well established to regulate and reprogram different redox and metabolic pathways under both pathological and physiological conditions. Therefore, alterations in Sirtuin levels can be a pivotal intermediary step in the pathogenesis of several disorders. This review first highlights the mechanisms involved in the regulation of Sirtuins and further summarizes the current findings on the major functions of Sirtuins in cellular redox homeostasis and bioenergetics (glucose and lipid metabolism).
引用
收藏
页数:13
相关论文
共 196 条
[1]
Phosphorylation of HuR by Chk2 regulates SIRT1 expression [J].
Abdelmohsen, Kotb ;
Pullmann, Rudolf, Jr. ;
Lai, Ashish ;
Kim, Hyeon Ho ;
Galban, Stefanie ;
Yang, Xiaoling ;
Blethrow, Justin D. ;
Walker, Mark ;
Shubert, Jonathan ;
Gillespie, David A. ;
Furneaux, Henry ;
Gorospe, Myriam .
MOLECULAR CELL, 2007, 25 (04) :543-557
[2]
Metabolic control by sirtuins and other enzymes that sense NAD+, NADH, or their ratio [J].
Anderson, Kristin A. ;
Madsen, Andreas S. ;
Olsen, Christian A. ;
Hirschey, Matthew D. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2017, 1858 (12) :991-998
[3]
Ubiquitin-Specific Peptidase U5P22 Negatively Regulates the STAT Signaling Pathway by Deubiquitinating SIRT1 [J].
Ao, Ning ;
Liu, Yanyan ;
Feng, Hailiang ;
Bian, Xiaocui ;
Li, Zhanwen ;
Gu, Bei ;
Zhao, Xiaomei ;
Liu, Yuqin .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2014, 33 (06) :1863-1875
[4]
SIRT1 regulates oxidant- and cigarette smoke-induced eNOS acetylation in endothelial cells: Role of resveratrol [J].
Arunachalam, Gnanapragasam ;
Yao, Hongwei ;
Sundar, Isaac K. ;
Caito, Samuel ;
Rahman, Irfan .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 393 (01) :66-72
[5]
Cancer Cell Survival Following DNA Damage-mediated Premature Senescence Is Regulated by Mammalian Target of Rapamycin (mTOR)-dependent Inhibition of Sirtuin 1 [J].
Back, Jung Ho ;
Rezvani, Hamid Reza ;
Zhu, Yucui ;
Guyonnet-Duperat, Veronique ;
Athar, Mohammad ;
Ratner, Desiree ;
Kim, Arianna L. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (21) :19100-19108
[6]
Resveratrol ameliorates cardiac oxidative stress in diabetes through deacetylation of NFkB-p65 and histone 3 [J].
Bagul, Pankaj K. ;
Deepthi, Nancy ;
Sultana, Razia ;
Banerjee, Sanjay K. .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2015, 26 (11) :1298-1307
[7]
Therapeutic potential of resveratrol:: the in vivo evidence [J].
Baur, Joseph A. ;
Sinclair, David A. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (06) :493-506
[8]
SirT3 suppresses hypoxia inducible factor 1α and tumor growth by inhibiting mitochondrial ROS production [J].
Bell, E. L. ;
Emerling, B. M. ;
Ricoult, S. J. H. ;
Guarente, L. .
ONCOGENE, 2011, 30 (26) :2986-2996
[9]
Slowing ageing by design: the rise of NAD+ and sirtuin-activating compounds [J].
Bonkowski, Michael S. ;
Sinclair, David A. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2016, 17 (11) :679-690
[10]
Stabilization of Suv39H1 by SirT1 Is Part of Oxidative Stress Response and Ensures Genome Protection [J].
Bosch-Presegue, Laia ;
Raurell-Vila, Helena ;
Marazuela-Duque, Anna ;
Kane-Goldsmith, Noriko ;
Valle, Adamo ;
Oliver, Jordi ;
Serrano, Lourdes ;
Vaquero, Alejandro .
MOLECULAR CELL, 2011, 42 (02) :210-223