A continuous correlation between oxidative stress and telomere shortening in fibroblasts

被引:234
作者
Richter, Torsten
von Zglinicki, Thomas [1 ]
机构
[1] Univ Newcastle, Inst Ageing & Hlth, Henry Wellcome Lab Biogerontol Res, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[2] Univ Newcastle, Ctr Integrated Syst Biol Ageing & Nutr, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
关键词
senescence; telomeres; oxidative stress; fibroblasts; antioxidative capacity; SINGLE-STRAND BREAKS; LENGTH; ANTIOXIDANT; MORTALITY; CELLS;
D O I
10.1016/j.exger.2007.08.005
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Telomere shortening in cells with low intrinsic telomerase activity like fibroblasts is governed by various mechanisms including the so-called end-replication problem, end processing and oxidative DNA damage. To assess the impact of oxidative stress on telomere shortening rates, we compared telomere shortening rates measured in fibroblasts from two different donor species (human and sheep) under both pro- and antioxidative culture regimes. Over an almost 50-fold change in peroxide indicator dye fluorescence intensity, we found a continuous, exponential correlation between cellular oxidative stress levels and telomere shortening rates, which was independent of donor species and cell strain. This correlation suggests stress-mediated telomere DNA damage as an important determinant of telomere shortening. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1039 / 1042
页数:4
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