Disruption of insulin signalling preserves bioenergetic competence of mitochondria in ageing Caenorhabditis elegans

被引:57
作者
Brys, Kristel [1 ]
Castelein, Natascha [1 ]
Matthijssens, Filip [1 ]
Vanfleteren, Jacques R. [1 ]
Braeckman, Bart P. [1 ]
机构
[1] Univ Ghent, Dept Biol, B-9000 Ghent, Belgium
关键词
LIFE-SPAN DETERMINATION; CYTOCHROME-C-OXIDASE; LIVED DAF-2 MUTANTS; OXIDATIVE STRESS; ELECTRON-TRANSPORT; METABOLIC-ACTIVITY; GENE-EXPRESSION; DAMAGE THEORY; LONGEVITY; LONG;
D O I
10.1186/1741-7007-8-91
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The gene daf-2 encodes the single insulin/insulin growth factor-1-like receptor of Caenorhabditis elegans. The reduction-of-function allele e1370 induces several metabolic alterations and doubles lifespan. Results: We found that the e1370 mutation alters aerobic energy production substantially. In wild-type worms the abundance of key mitochondrial proteins declines with age, accompanied by a dramatic decrease in energy production, although the mitochondrial mass, inferred from the mitochondrial DNA copy number, remains unaltered. In contrast, the age-dependent decrease of both key mitochondrial proteins and bioenergetic competence is considerably attenuated in daf-2(e1370) adult animals. The increase in daf-2(e1370) mitochondrial competence is associated with a higher membrane potential and increased reactive oxygen species production, but with little damage to mitochondrial protein or DNA. Together these results point to a higher energetic efficiency of daf-2(e1370) animals. Conclusions: We conclude that low daf-2 function alters the overall rate of ageing by a yet unidentified mechanism with an indirect protective effect on mitochondrial function.
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页数:15
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