Stress, DNA damage and ageing -: an integrative approach

被引:143
作者
von Zglinicki, T [1 ]
Bürkle, A [1 ]
Kirkwood, TBL [1 ]
机构
[1] Newcastle Univ, Newcastle Gen Hosp, Wolfson Res Ctr, Inst Hlth Elderly,Dept Gerontol, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
关键词
cell replicative senescence; stress; oxidative damage; DNA repair; telomere loss; poly(ADP-ribose)polymerase (PARP); mitochondrial mutations; mathematical models;
D O I
10.1016/S0531-5565(01)00111-5
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
Ageing is highly complex, involving multiple mechanisms at different levels. Nevertheless, recent evidence suggests that several of the most important mechanisms are linked via endogenous stress-induced DNA damage caused by reactive oxygen species (ROS). Understanding how such damage contributes to age-related changes requires that we explain how these different mechanisms relate to each other and potentially interact. In this article, we review the contributions of stress-induced damage to cellular DNA through (i) the role of damage to nuclear DNA and its repair mediated via the actions of poly(ADP-ribose) polymerase-1, (ii) the role of damage to telomeric DNA and its contribution to telomere-driven cell senescence, and (iii) the role of damage to and the accumulation of mutations in mitochondrial DNA. We describe how an integrative approach to studying these mechanisms, coupled with computational modelling, may be of considerable importance in resolving some of the complexity of cellular ageing. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1049 / 1062
页数:14
相关论文
共 89 条
[1]   Selective loss of poly(ADP-ribose) and the 85-kDa fragment of poly(ADP-ribose) polymerase in nucleoli during alkylation-induced apoptosis of HeLa cells [J].
Alvarez-Gonzalez, R ;
Spring, H ;
Müller, M ;
Bürkle, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32122-32126
[2]   Telomere states and cell fates [J].
Blackburn, EH .
NATURE, 2000, 408 (6808) :53-56
[3]   Extension of life-span by introduction of telomerase into normal human cells [J].
Bodnar, AG ;
Ouellette, M ;
Frolkis, M ;
Holt, SE ;
Chiu, CP ;
Morin, GB ;
Harley, CB ;
Shay, JW ;
Lichtsteiner, S ;
Wright, WE .
SCIENCE, 1998, 279 (5349) :349-352
[4]   Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscle [J].
Brierley, EJ ;
Johnson, MA ;
Lightowlers, RN ;
James, OFW ;
Turnbull, DM .
ANNALS OF NEUROLOGY, 1998, 43 (02) :217-223
[5]   Poly(ADP-ribose) immunostaining to detect apoptosis induced by a neurotoxic fragment of prion protein [J].
Bürkle, A ;
Kretzschmar, HA ;
Brown, DR .
HISTOCHEMICAL JOURNAL, 1999, 31 (11) :711-716
[6]  
Bürkle A, 2000, ANN NY ACAD SCI, V908, P126
[7]   Poly(ADP-ribosyl)ation:: a posttranslational protein modification linked with genome protection and mammalian longevity [J].
Bürkle, A .
BIOGERONTOLOGY, 2000, 1 (01) :41-46
[8]  
Campisi J, 1999, MOLECULAR BASIS OF CELL CYCLE AND GROWTH CONTROL, P348
[9]  
CAMPISI J, 1996, HDB BIOL AGING, V1, P121
[10]   TELOMERE LENGTH AND REPLICATIVE AGING IN HUMAN VASCULAR TISSUES [J].
CHANG, E ;
HARLEY, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) :11190-11194