Autophagy is required for dietary restriction-mediated life span extension in C-elegans

被引:241
作者
Jia, Kailiang
Levine, Beth
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA
关键词
autophagy; C; elegans; aging; starvation; longevity;
D O I
10.4161/auto.4989
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dietary restriction extends life span in diverse species including Caenorhabditis elegans. However, the downstream cellular targets regulated by dietary restriction are largely unknown. Autophagy, an evolutionary conserved lysosomal degradation pathway, is induced under starvation conditions and regulates life span in insulin signaling C. elegans mutants. We now report that two essential autophagy genes (bec-1 and Ce-atg7) are required for the longevity phenotype of the C. elegans dietary restriction mutant (eat-2(ad 1113) animals. Thus, we propose that autophagy mediates the effect, not only of insulin signaling, but also of dietary restriction on the regulation of C. elegans life span. Since autophagy and longevity control are highly conserved from C. elegans to mammals, a similar role for autophagy in dietary restriction-mediated life span extension may also exist in mammals.
引用
收藏
页码:597 / 599
页数:3
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