mTOR, AMPK, and Sirt1: Key Players in Metabolic Stress Management

被引:74
作者
Cetrullo, Silvia [1 ]
D'Adamo, Stefania [1 ]
Tantini, Benedetta [1 ]
Borzi, Rosa Maria [2 ,3 ]
Flamigni, Flavio [1 ]
机构
[1] Univ Bologna, Dipartimento Sci Biomed & Neuromotorie, I-40126 Bologna, Italy
[2] Ist Ortoped Rizzoli, Lab Immunoreumatol & Rigeneraz Tessutale, Bologna, Italy
[3] Ist Ortoped Rizzoli, Dipartimento RIT, Lab RAMSES, Bologna, Italy
来源
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION | 2015年 / 25卷 / 01期
关键词
mTOR; AMPK; Sirt1; autophagy; ACTIVATED PROTEIN-KINASE; ACETYL-COA CARBOXYLASE; PROGRAMMED CELL-DEATH; SKELETAL-MUSCLE; MAMMALIAN TARGET; AMINO-ACIDS; DEACETYLASE SIRT1; HEPATIC STEATOSIS; CARDIAC MYOBLASTS; INHIBITS MTORC2;
D O I
10.1615/CritRevEukaryotGeneExpr.2015012975
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cells adapt their metabolism and activities in response to signals from their surroundings, and this ability is essential for their survival in the face of environmental changes. In mammalian tissues a deficit of these mechanisms is commonly associated with cellular aging and degenerative diseases related to aging, such as cardiovascular disease, cancer, immune system decline, and neurological pathologies. Several proteins have been identified as able to respond directly to energy, nutrient, and growth factor levels and stress stimuli in order to mediate adaptations in the cell. Many of these proteins are enzymes that positively or negatively modulate the autophagic process. This review focuses on biochemical mechanisms involving enzymes-specifically, mTOR, AMPK, and Sirt1-that are currently considered important for these adaptive responses, providing an overview of the interactions of the main players in this process.
引用
收藏
页码:59 / 75
页数:17
相关论文
共 115 条
[11]   AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity [J].
Canto, Carles ;
Gerhart-Hines, Zachary ;
Feige, Jerome N. ;
Lagouge, Marie ;
Noriega, Lilia ;
Milne, Jill C. ;
Elliott, Peter J. ;
Puigserver, Pere ;
Auwerx, Johan .
NATURE, 2009, 458 (7241) :1056-U140
[12]   THE SUBSTRATE AND SEQUENCE SPECIFICITY OF THE AMP-ACTIVATED PROTEIN-KINASE - PHOSPHORYLATION OF GLYCOGEN-SYNTHASE AND PHOSPHORYLASE-KINASE [J].
CARLING, D ;
HARDIE, DG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1012 (01) :81-86
[13]   Antiapoptotic and Antiautophagic Effects of Eicosapentaenoic Acid in Cardiac Myoblasts Exposed to Palmitic Acid [J].
Cetrullo, Silvia ;
Tantini, Benedetta ;
Flamigni, Flavio ;
Pazzini, Claudia ;
Facchini, Annalisa ;
Stefanelli, Claudio ;
Caldarera, Claudio M. ;
Pignatti, Carla .
NUTRIENTS, 2012, 4 (02) :78-90
[14]   A pro-survival effect of polyamine depletion on norepinephrine-mediated apoptosis in cardiac cells: role of signaling enzymes [J].
Cetrullo, Silvia ;
Tantini, Benedetta ;
Facchini, Annalisa ;
Pignatti, Carla ;
Stefanelli, Claudio ;
Caldarera, Claudio Marcello ;
Flamigni, Flavio .
AMINO ACIDS, 2011, 40 (04) :1127-1137
[15]   FoxOs Inhibit mTORC1 and Activate Akt by Inducing the Expression of Sestrin3 and Rictor [J].
Chen, Chia-Chen ;
Jeon, Sang-Min ;
Bhaskar, Prashanth T. ;
Nogueira, Veronique ;
Sundararajan, Deepa ;
Tonic, Ivana ;
Park, Youngkyu ;
Hay, Nissim .
DEVELOPMENTAL CELL, 2010, 18 (04) :592-604
[16]   ER Stress Inhibits mTORC2 and Akt Signaling Through GSK-3β-Mediated Phosphorylation of Rictor [J].
Chen, Chien-Hung ;
Shaikenov, Tattym ;
Peterson, Timothy R. ;
Aimbetov, Rakhan ;
Bissenbaev, Amangeldy K. ;
Lee, Szu-Wei ;
Wu, Juan ;
Lin, Hui-Kuan ;
Sarbassov, Dos D. .
SCIENCE SIGNALING, 2011, 4 (161)
[17]  
Chen S, BIOCH J, V409, P449
[18]   Characterization of AMP-activated protein kinase γ-subunit isoforms and their role in AMP binding [J].
Cheung, PCF ;
Salt, IP ;
Davies, SP ;
Hardie, DG ;
Carling, D .
BIOCHEMICAL JOURNAL, 2000, 346 :659-669
[19]   REGULATION OF HMG-COA REDUCTASE - IDENTIFICATION OF THE SITE PHOSPHORYLATED BY THE AMP-ACTIVATED PROTEIN-KINASE INVITRO AND IN INTACT RAT-LIVER [J].
CLARKE, PR ;
HARDIE, DG .
EMBO JOURNAL, 1990, 9 (08) :2439-2446
[20]   Gain-of-Function R225W Mutation in Human AMPKγ3 Causing Increased Glycogen and Decreased Triglyceride in Skeletal Muscle [J].
Costford, Sheila R. ;
Kavaslar, Nihan ;
Ahituv, Nadav ;
Chaudhry, Shehla N. ;
Schackwitz, Wendy S. ;
Dent, Robert ;
Pennacchio, Len A. ;
McPherson, Ruth ;
Harper, Mary-Ellen .
PLOS ONE, 2007, 2 (09)