D-amino acid oxidase promotes cellular senescence via the production of reactive oxygen species

被引:28
作者
Nagano, Taiki [1 ,2 ]
Yamao, Shunsuke [2 ]
Terachi, Anju [2 ]
Yarimizu, Hidetora [2 ]
Itoh, Haruki [2 ]
Katasho, Ryoko [3 ]
Kawai, Kosuke [2 ]
Nakashima, Akio [1 ,4 ]
Iwasaki, Tetsushi [1 ,2 ,3 ]
Kikkawa, Ushio [1 ,4 ]
Kamada, Shinji [1 ,2 ,3 ]
机构
[1] Kobe Univ, Biosignal Res Ctr, Kobe, Hyogo, Japan
[2] Kobe Univ, Grad Sch Sci, Dept Biol, Kobe, Hyogo, Japan
[3] Kobe Univ, Fac Sci, Dept Biol, Kobe, Hyogo, Japan
[4] Kobe Univ, Grad Sch Agr Sci, Dept Bioresource Sci, Kobe, Hyogo, Japan
基金
日本学术振兴会;
关键词
DNA-DAMAGE; D-SERINE; NAD(P)H OXIDASE; TUMOR-CELLS; D-ASPARTATE; P53; GENERATION; PROLINE; MICE; IDENTIFICATION;
D O I
10.26508/lsa.201800045
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
D-amino acid oxidase (DAO) is a flavin adenine dinucleotide (FAD)-dependent oxidase metabolizing neutral and polar D-amino acids. Unlike L-amino acids, the amounts of D-amino acids in mammalian tissues are extremely low, and therefore, little has been investigated regarding the physiological role of DAO. We have recently identified DAO to be up-regulated in cellular senescence, a permanent cell cycle arrest induced by various stresses, such as persistent DNA damage and oxidative stress. Because DAO produces reactive oxygen species (ROS) as byproducts of substrate oxidation and the accumulation of ROS mediates the senescence induction, we explored the relationship between DAO and senescence. We found that inhibition of DAO impaired senescence induced by DNA damage, and ectopic expression of wild-type DAO, but not enzymatically inactive mutant, enhanced it in an ROS-dependent manner. Furthermore, addition of D-amino acids and riboflavin, a metabolic precursor of FAD, to the medium potentiated the senescence-promoting effect of DAO. These results indicate that DAO promotes senescence through the enzymatic ROS generation, and its activity is regulated by the availability of its substrate and coenzyme.
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页数:14
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共 57 条
[1]  
BASS DA, 1983, J IMMUNOL, V130, P1910
[2]   D-Amino acids in brain neurotransmission and synaptic plasticity [J].
Billard, Jean-Marie .
AMINO ACIDS, 2012, 43 (05) :1851-1860
[3]   Distinct p53 Transcriptional Programs Dictate Acute DNA-Damage Responses and Tumor Suppression [J].
Brady, Colleen A. ;
Jiang, Dadi ;
Mello, Stephano S. ;
Johnson, Thomas M. ;
Jarvis, Lesley A. ;
Kozak, Margaret M. ;
Broz, Daniela Kenzelmann ;
Basak, Shashwati ;
Park, Eunice J. ;
McLaughlin, Margaret E. ;
Karnezis, Anthony N. ;
Attardi, Laura D. .
CELL, 2011, 145 (04) :571-583
[4]   Aging, Cellular Senescence, and Cancer [J].
Campisi, Judith .
ANNUAL REVIEW OF PHYSIOLOGY, VOL 75, 2013, 75 :685-705
[5]   SENESCENCE-LIKE GROWTH ARREST INDUCED BY HYDROGEN-PEROXIDE IN HUMAN-DIPLOID FIBROBLAST F65 CELLS [J].
CHEN, Q ;
AMES, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) :4130-4134
[6]   D-amino acids in normal ageing and pathogenesis of neurodegenerative diseases [J].
Chervyakov, A. V. ;
Gulyaeva, N. V. ;
Zakharova, M. N. .
NEUROCHEMICAL JOURNAL, 2011, 5 (02) :100-114
[7]   FURTHER STUDY ON THE SPECIFICITY OF D-AMINO-ACID OXIDASE AND OF D-ASPARTATE OXIDASE AND TIME-COURSE FOR COMPLETE OXIDATION OF D-AMINO ACIDS [J].
DANIELLO, A ;
VETERE, A ;
PETRUCELLI, L .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1993, 105 (3-4) :731-734
[8]   Mitochondrial function and toxicity: Role of the B vitamin family on mitochondrial energy metabolism [J].
Depeint, Flore ;
Bruce, W. Robert ;
Shangari, Nandita ;
Mehta, Rhea ;
O'Brien, Peter J. .
CHEMICO-BIOLOGICAL INTERACTIONS, 2006, 163 (1-2) :94-112
[9]   Living on a break: cellular senescence as a DNA-damage response [J].
di Fagagna, Fabrizio d'Adda .
NATURE REVIEWS CANCER, 2008, 8 (07) :512-522
[10]   DNA-DAMAGE TRIGGERS A PROLONGED P53-DEPENDENT G(1) ARREST AND LONG-TERM INDUCTION OF CIP1 IN NORMAL HUMAN FIBROBLASTS [J].
DI LEONARDO, A ;
LINKE, SP ;
CLARKIN, K ;
WAHL, GM .
GENES & DEVELOPMENT, 1994, 8 (21) :2540-2551