Lysosomal signaling molecules regulate longevity in <i>Caenorhabditis elegans</i>

Andrew Folick(Baylor College of Medicine), Holly D. Oakley(Baylor College of Medicine), Yong Yu(Baylor College of Medicine), Eric H. Armstrong(Emory University), Manju Kumari(University of Graz), Lucas Sanor(Baylor College of Medicine), David D. Moore(Baylor College of Medicine), Eric A. Ortlund(Emory University), Rudolf Zechner(University of Graz), Meng C. Wang(Baylor College of Medicine)
Science
January 1, 2015
Cited by 286

Abstract

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.


Related Papers