4.8 Article

Lysosomal signaling molecules regulate longevity in Caenorhabditis elegans

期刊

SCIENCE
卷 347, 期 6217, 页码 83-86

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1258857

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资金

  1. NIH [T32GM008602, R01DK095750, T32HD055200, F30AG046043, R00AG034988, R01AG045183]
  2. Ellison New Scholar Award
  3. Welch Chair in Science [Q-0022]
  4. European Research Council Advanced Grant
  5. Fondation Leducq
  6. Austrian Science Fund (FWF) [Z 136, F 3002] Funding Source: researchfish

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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.

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