Reactive oxygen species and age-related genes p66Shc, sirtuin, FoxO3 and klotho in senescence

被引:22
作者
Afanas'ev, Igor [1 ]
机构
[1] All Union Vitamin Res Inst, Moscow, Russia
关键词
ROS signaling; genes; senescence; aging; FORKHEAD TRANSCRIPTION FACTOR; ACTIVATED PROTEIN-KINASE; OXIDATIVE STRESS; LIFE-SPAN; DOWN-REGULATION; ENDOTHELIAL-CELLS; HYDROGEN-PEROXIDE; ADAPTER PROTEIN; COENZYME Q(10); NITRIC-OXIDE;
D O I
10.4161/oxim.3.2.11050
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Reactive oxygen species (ROS) superoxide and hydrogen peroxide perform important signaling functions in many physiological and pathophysiological processes. Cell senescence and organismal age are not exemptions. Aging-regulating genes p66shc, Sirtuin, FOXO3a and Klotho are new important factors which are stimulated by ROS signaling. It has been shown that ROS participate in initiation and prolongation of gene-dependent aging development. ROS also participate in the activation of protein kinases Akt/PKB and extracellular signal-regulated kinase ERK, which by themselves or through gene activation stimulates or retards cell senescence. Different retarding/stimulating effects of ROS might depend on the nature of signaling species-superoxide or hydrogen peroxide. Importance of radical anion superoxide as a signaling molecule with "super-nucleophilic" properties points to the possibility of the use of superoxide scavengers (SOD mimetics, ubiquinones and flavonoids) for retarding the development of aging.
引用
收藏
页码:77 / 85
页数:9
相关论文
共 65 条
[11]   Inhibition of wild-type p66ShcA in mesangial cells prevents glycooxidant-dependent FOXO3a regulation and promotes the survival phenotype [J].
Chintapalli, Janaki ;
Yang, Shuo ;
Opawumi, David ;
Goyal, Sunita Ray ;
Shamsuddin, Nazia ;
Malhotra, Ashwani ;
Reiss, Krzysztof ;
Meggs, Leonard G. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2007, 292 (02) :F523-F530
[12]   Alterations of nitric oxide synthase expression with aging and hypertension in rats [J].
Chou, TC ;
Yen, MH ;
Li, CY ;
Ding, YA .
HYPERTENSION, 1998, 31 (02) :643-648
[13]  
CLAUSEN A, 2008, NEUROBIOL AGING, V18
[14]   Age-Accelerated Atherosclerosis Correlates With Failure to Upregulate Antioxidant Genes [J].
Collins, Alan R. ;
Lyon, Christopher J. ;
Xia, Xuefeng ;
Liu, Joey Z. ;
Tangirala, Rajendra K. ;
Yin, Fen ;
Boyadjian, Rima ;
Bikineyeva, Alfiya ;
Pratico, Domenico ;
Harrison, David G. ;
Hsueh, Willa A. .
CIRCULATION RESEARCH, 2009, 104 (06) :e42-E54
[15]   AMPKα1 regulates the antioxidant status of vascular endothelial cells [J].
Colombo, Sergio L. ;
Moncada, Salvador .
BIOCHEMICAL JOURNAL, 2009, 421 :163-169
[16]   Arachidonic acid activates c-jun N-terminal kinase through NADPH oxidase in rabbit proximal tubular epithelial cells [J].
Cui, XL ;
Douglas, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :3771-3776
[17]   Discrete generation of superoxide and hydrogen peroxide by T cell receptor stimulation: Selective regulation of mitogen-activated protein kinase activation and Fas ligand expression [J].
Devadas, S ;
Zaritskaya, L ;
Rhee, SG ;
Oberley, L ;
Williams, MS .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (01) :59-70
[18]   Activation of the lifespan regulator p66Shc through reversible disulfide bond formation [J].
Gertz, Melanie ;
Fischer, Frank ;
Wolters, Dirk ;
Steegborn, Clemens .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (15) :5705-5709
[19]   Electron transfer between cytochrome c and p66Shc generates reactive oxygen species that trigger mitochondrial apoptosis [J].
Giorgio, M ;
Migliaccio, E ;
Orsini, F ;
Paolucci, D ;
Moroni, M ;
Contursi, C ;
Pelliccia, G ;
Luzi, L ;
Minucci, S ;
Marcaccio, M ;
Pinton, P ;
Rizzuto, R ;
Bernardi, P ;
Paolucci, F ;
Pelicci, PG .
CELL, 2005, 122 (02) :221-233
[20]   p66Shc Links α1-Adrenergic Receptors to a Reactive Oxygen Species-Dependent AKT-FOXO3A Phosphorylation Pathway in Cardiomyocytes [J].
Guo, Jianfen ;
Gertsberg, Zoya ;
Ozgen, Nazira ;
Steinberg, Susan F. .
CIRCULATION RESEARCH, 2009, 104 (05) :660-669