Age-related cellular changes in the long-lived bivalve A. islandica

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作者
Heike Gruber
Wiebke Wessels
Primrose Boynton
Jinze Xu
Stephanie Wohlgemuth
Christiaan Leeuwenburgh
Wenbo Qi
Steven N. Austad
Ralf Schaible
Eva E. R. Philipp
机构
[1] Max-Planck-Institute for Evolutionary Biology,ARC Centre of Excellence for Coral Reef Studies and School of Pharmacy and Molecular Sciences
[2] James Cook University,Department of Aging & Geriatric Research
[3] University of Florida,Department of Animal Sciences, College of Agriculture and Life Science/IFAS
[4] University of Florida,UT Health Science Center San Antonio
[5] Barshop Institute for Longevity and Aging Studies,Institute of Clinical Molecular Biology
[6] Max-Planck-Institute for Demographic Research,Department of Biology
[7] University Hospital Schleswig Holstein,undefined
[8] University of Alabama at Birmingham,undefined
来源
AGE | 2015年 / 37卷
关键词
Longevity; Aging marker; Oxidation; Cellular maintenance;
D O I
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摘要
One of the biggest challenges to studying causes and effects of aging is identifying changes in cells that are related to senescence instead of simply the passing of chronological time. We investigated two populations of the longest living non-colonial metazoan, Arctica islandica, with lifespans that differed sixfolds. Of four investigated parameters (nucleic acid oxidation, protein oxidation, lipid oxidation, and protein instability), only nucleic acid oxidation increased with age and correlated with relative lifespan. Nucleic acid oxidation levels increased significantly faster and were significantly higher in the shorter-lived than the longer-lived population. In contrast, neither protein oxidation, lipid oxidation, nor protein stability changed over time. Protein resistance to unfolding stress when treated with urea was significantly lower overall in the shorter-lived population, and lipid peroxidation levels were higher in the longer-lived population. With the exception of nucleic acid oxidation, damage levels of A. islandica do not change with age, indicating excellent cellular maintenance in both populations. Since correlations between nucleic acid oxidation and age have also been shown previously in other organisms, and nucleic acid oxidation accumulation rate correlates with relative age in both investigated populations, nucleic acid oxidation may reflect intrinsic aging mechanisms.
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