Dietary restriction suppresses proteotoxicity and enhances longevity by an hsf-1-dependent mechanism in Caenorhabditis elegans

被引:193
|
作者
Steinkraus, Katherine A. [1 ]
Smith, Erica D. [1 ,2 ]
Davis, Christina [1 ]
Carr, Daniel [1 ]
Pendergrass, William R. [1 ]
Sutphin, George L. [1 ]
Kennedy, Brian K. [2 ]
Kaeberlein, Matt [1 ]
机构
[1] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
关键词
Caenorhabditis elegans; dietary restriction; hsf-1; longevity; proteotoxicitys;
D O I
10.1111/j.1474-9726.2008.00385.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dietary restriction increases lifespan and slows the onset of age-associated disease in organisms from yeast to mammals. In humans, several age-related diseases are associated with aberrant protein folding or aggregation, including neurodegenerative disorders such as Alzheimer's, Parkinson's, and Huntington's diseases. We report here that dietary restriction dramatically suppresses age-associated paralysis in three nematode models of proteotoxicity. Similar to its longevity-enhancing properties, dietary restriction protects against proteotoxicity by a mechanism distinct from reduced insulin/IGF-1-like signaling. Instead, the heat shock transcription factor, hsf-1, is required for enhanced thermotolerance, suppression of proteotoxicity, and lifespan extension by dietary restriction. These findings demonstrate that dietary restriction confers a general protective effect against proteotoxicity and promotes longevity by a mechanism involving hsf-1.
引用
收藏
页码:394 / 404
页数:11
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