RRC ID 54826
Author Nagano T, Yamao S, Terachi A, Yarimizu H, Itoh H, Katasho R, Kawai K, Nakashima A, Iwasaki T, Kikkawa U, Kamada S.
Title d-amino acid oxidase promotes cellular senescence via the production of reactive oxygen species.
Journal Life Sci Alliance
Abstract 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.
Volume 2(1)
Published 2019-2-1
DOI 10.26508/lsa.201800045
PII 2/1/e201800045
PMID 30659069
PMC PMC6339261
MeSH Amino Acids / metabolism Arginine / metabolism Cellular Senescence / drug effects Cellular Senescence / physiology* Coenzymes / metabolism D-Amino-Acid Oxidase / antagonists & inhibitors D-Amino-Acid Oxidase / genetics* D-Amino-Acid Oxidase / metabolism* DNA Damage / genetics Flavin-Adenine Dinucleotide / metabolism Gene Knockdown Techniques Hep G2 Cells Humans Oxidation-Reduction RNA Interference Reactive Oxygen Species / metabolism* Riboflavin / pharmacology Serine / metabolism Transfection
IF 2.622
Times Cited 3
Resource
Human and Animal Cells WI-38(RCB0702)