Genetics, Life Span, Health Span, and the Aging Process in Caenorhabditis elegans

被引:73
|
作者
Tissenbaum, Heidi A. [1 ]
机构
[1] Univ Massachusetts, Program Gene Funct & Express, Program Mol Med, Sch Med, Worcester, MA 01605 USA
关键词
Life span; Aging; Health span; C; elegans; Genetics; LIVED DAF-2 MUTANTS; HEAT-SHOCK FACTOR; C-ELEGANS; DIETARY RESTRICTION; REGULATES LONGEVITY; DAUER FORMATION; TGF-BETA; GENES; LONG; NEMATODE;
D O I
10.1093/gerona/gls088
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
As a tool for measuring the aging process, life span has been invaluable in dissecting the genes that modulate longevity. Studies over the past few decades have identified several hundred genes that can modify life span in model organisms such as yeast, worms, and flies. Yet, despite this vast amount of research, we still do not fully understand how the genes that affect life span influence how an organism ages. How does modulation of the genes that affect life span contribute to the aging process? Does life-span extension result in extension of healthy aging? Here, we will focus primarily on the insulin/IGF-1 signaling pathway in Caenorhabditis elegans because members of this pathway have been shown to be associated with extended life span across phylogeny, from worms to humans. I discuss how this connects to the aging process, age-associated disease, and the potential to increase healthy aging in addition to lengthening life span.
引用
收藏
页码:503 / 510
页数:8
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