Differential patterns of apoptosis in response to aging in Drosophila

被引:78
作者
Zheng, A
Edelman, SW
Tharmarajah, G
Walker, DW
Pletcher, SD
Seroude, L
机构
[1] Queens Univ, Dept Biol, Kingston, ON K7L 3N6, Canada
[2] CALTECH, Div Biol, Pasadena, CA 91125 USA
[3] Baylor Coll Med, Huffington Ctr Aging & Mol & Human Genet, Houston, TX 77030 USA
关键词
oxidative stress;
D O I
10.1073/pnas.0503374102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several lines of evidence suggest that programmed cell death may play a role in the aging process and the age-related functional declines of multicellular organisms. To pave the way for the use of Drosophila to rigorously test this hypothesis in a genetic model organism, this work examines the pattern of apoptosis in the adult fly during aging. The analysis across the lifespan of caspase activity and DNA fragmentation shows that apoptosis occurs in adult flies at all ages and that it is linked to physiological age. The results establish that under normal conditions, fly aging is coupled with a lifelong gradual increase of apoptosis within muscle cells and an activation of apoptosis in fat cells of old flies. The nervous system does not show signs of apoptosis. These time- and tissue-specific changes indicate that aging influences the levels and the nature of the cells that commit to apoptosis. The comparison with the apoptotic response to starvation and oxidative stresses strongly suggests that the lifelong increase in flight and leg muscles results from the accumulation of oxidative damage associated with aging. This finding presents an attractive mechanism to account for the decline of locomotor functions and muscle loss in the elderly and opens the way for the genetic analysis of sarcopenia in Drosophila.
引用
收藏
页码:12083 / 12088
页数:6
相关论文
共 49 条
[1]   Ways of dying: multiple pathways to apoptosis [J].
Adams, JM .
GENES & DEVELOPMENT, 2003, 17 (20) :2481-2495
[2]   FINE-STRUCTURAL CHANGES IN THE MIDGUT OF OLD DROSOPHILA-MELANOGASTER [J].
ANTONERXLEBEN, F ;
MIQUEL, J ;
PHILPOTT, DE .
MECHANISMS OF AGEING AND DEVELOPMENT, 1983, 23 (3-4) :265-276
[3]   Caspase activity and a specific cytochrome c are required for sperm differentiation in Drosophila [J].
Arama, E ;
Agapite, J ;
Steller, H .
DEVELOPMENTAL CELL, 2003, 4 (05) :687-697
[4]   GENETIC ALTERATION OF NORMAL AGING PROCESSES IS RESPONSIBLE FOR EXTENDED LONGEVITY IN DROSOPHILA [J].
ARKING, R ;
WELLS, RA .
DEVELOPMENTAL GENETICS, 1990, 11 (02) :141-148
[5]   Cellular senescence and apoptosis: how cellular responses might influence aging phenotypes [J].
Campisi, J .
EXPERIMENTAL GERONTOLOGY, 2003, 38 (1-2) :5-11
[6]   Dissociation between functional senescence and oxidative stress resistance in Drosophila [J].
Cook-Wiens, E ;
Grotewiel, MS .
EXPERIMENTAL GERONTOLOGY, 2002, 37 (12) :1347-1357
[7]   Apoptosis in skeletal muscle with aging [J].
Dirks, A ;
Leeuwenburgh, C .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 282 (02) :R519-R527
[8]   Aging and sarcopenia [J].
Doherty, TJ .
JOURNAL OF APPLIED PHYSIOLOGY, 2003, 95 (04) :1717-1727
[9]  
Draizen TA, 1999, J NEUROBIOL, V38, P455, DOI 10.1002/(SICI)1097-4695(199903)38:4<455::AID-NEU2>3.0.CO
[10]  
2-F