학술논문
Chronological Age and DNA Damage Accumulation in Blood Mononuclear Cells: A Linear Association in Healthy Humans after 50 Years of Age.
Document Type
Article
Author
Vlachogiannis, Nikolaos I.; Ntouros, Panagiotis A.; Pappa, Maria; Kravvariti, Evrydiki; Kostaki, Evangelia Georgia; Fragoulis, Georgios E.; Papanikolaou, Christina; Mavroeidi, Dimitra; Bournia, Vasiliki-Kalliopi; Panopoulos, Stylianos; Laskari, Katerina; Arida, Aikaterini; Gorgoulis, Vassilis G.; Tektonidou, Maria G.; Paraskevis, Dimitrios; Sfikakis, Petros P.; Souliotis, Vassilis L.
Source
Subject
*DNA damage
*AGE
*DNA repair
*BLOOD cells
*MONONUCLEAR leukocytes
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Language
ISSN
1661-6596
Abstract
Aging is characterized by the progressive deregulation of homeostatic mechanisms causing the accumulation of macromolecular damage, including DNA damage, progressive decline in organ function and chronic diseases. Since several features of the aging phenotype are closely related to defects in the DNA damage response (DDR) network, we have herein investigated the relationship between chronological age and DDR signals in peripheral blood mononuclear cells (PBMCs) from healthy individuals. DDR-associated parameters, including endogenous DNA damage (single-strand breaks and double-strand breaks (DSBs) measured by the alkaline comet assay (Olive Tail Moment (OTM); DSBs-only by γH2AX immunofluorescence staining), DSBs repair capacity, oxidative stress, and apurinic/apyrimidinic sites were evaluated in PBMCs of 243 individuals aged 18–75 years, free of any major comorbidity. While OTM values showed marginal correlation with age until 50 years (rs = 0.41, p = 0.11), a linear relationship was observed after 50 years (r = 0.95, p < 0.001). Moreover, individuals older than 50 years showed increased endogenous DSBs levels (γH2Ax), higher oxidative stress, augmented apurinic/apyrimidinic sites and decreased DSBs repair capacity than those with age lower than 50 years (all p < 0.001). Results were reproduced when we examined men and women separately. Prospective studies confirming the value of DNA damage accumulation as a biomarker of aging, as well as the presence of a relevant agethreshold, are warranted. [ABSTRACT FROM AUTHOR]