Lysosomal signaling molecules regulate longevity in Caenorhabditis elegans

被引:186
作者
Folick, Andrew [1 ]
Oakley, Holly D. [2 ,3 ]
Yu, Yong [2 ,3 ]
Armstrong, Eric H. [4 ]
Kumari, Manju [5 ]
Sanor, Lucas [2 ]
Moore, David D. [1 ,6 ]
Ortlund, Eric A. [4 ]
Zechner, Rudolf [5 ]
Wang, Meng C. [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Huffington Ctr Aging, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[4] Emory Univ, Sch Med, Winship Canc Inst, Dept Biochem Discovery & Dev Therapeut, Atlanta, GA 30322 USA
[5] Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria
[6] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
基金
欧洲研究理事会;
关键词
ACID-BINDING PROTEINS; C-ELEGANS; OLEOYLETHANOLAMIDE; RESTRICTION; METABOLISM; DIET;
D O I
10.1126/science.1258857
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lysosomes are crucial cellular organelles for human health that function in digestion and recycling of extracellular and intracellular macromolecules. We describe a signaling role for lysosomes that affects aging. In the worm Caenorhabditis elegans, the lysosomal acid lipase LIPL-4 triggered nuclear translocalization of a lysosomal lipid chaperone LBP-8, which promoted longevity by activating the nuclear hormone receptors NHR-49 and NHR-80. We used high-throughput metabolomic analysis to identify several lipids in which abundance was increased in worms constitutively overexpressing LIPL-4. Among them, oleoylethanolamide directly bound to LBP-8 and NHR-80 proteins, activated transcription of target genes of NHR-49 and NHR-80, and promoted longevity in C. elegans. These findings reveal a lysosome-to-nucleus signaling pathway that promotes longevity and suggest a function of lysosomes as signaling organelles in metazoans.
引用
收藏
页码:83 / 86
页数:4
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