Delayed behavioural aging and altered mortality in Drosophila β integrin mutants

被引:50
作者
Goddeeris, MM
Cook-Wiens, E
Horton, WJ
Wolf, H
Stoltzfus, JR
Borrusch, M
Grotewiel, MS
机构
[1] Michigan State Univ, Dept Zool, Grad Program Genet, E Lansing, MI 48824 USA
[2] Michigan State Univ, Neurosci Program, E Lansing, MI 48824 USA
来源
AGING CELL | 2003年 / 2卷 / 05期
关键词
aging; behaviour; geotaxis; integrin; lifespan; mortality;
D O I
10.1046/j.1474-9728.2003.00060.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The genetic basis for aging is being intensely investigated in a variety of model systems. Much of the focus in Drosophila has been on the molecular-genetic determinants of lifespan, whereas the molecular-genetic basis for age-related functional declines has been less vigorously explored. We evaluated behavioural aging and lifespan in flies harbouring loss-of-function mutations in myospheroid, the gene that encodes betaPS, a beta integrin. Integrins are adhesion molecules that regulate a number of cellular processes and developmental events. Their role in aging, however, has received limited attention. We report here that age-related declines in locomotor activity are ameliorated and that mean lifespan is increased in myospheroid mutants. The delayed functional senescence and altered mortality in myospheroid flies are independent of changes in body size, reproduction or stress resistance. Our data indicate that functional senescence and age-dependent mortality are influenced by beta integrins in Drosophila.
引用
收藏
页码:257 / 264
页数:8
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