Autophagy links lipid metabolism to longevity in C. elegans

Autophagy. 2012 Jan;8(1):144-6. doi: 10.4161/auto.8.1.18722. Epub 2012 Jan 1.

Abstract

The cellular recycling process of autophagy is emerging as a central player in many of the conserved longevity pathways in C. elegans, but the underlying mechanisms that link autophagy and life span remain unclear. In a recent study, we provided evidence to suggest that autophagy modulates aging through an effect on lipid homeostasis. Specifically, we identified a role for autophagy in a longevity model in which germline removal in C. elegans extends life span. Life-span extension in these animals is achieved, at least in part, through increased expression of the lipase LIPL-4. We found that autophagy and LIPL-4-dependent lipolysis are both upregulated in germline-less animals and work interdependently to prolong life span. While these genetic results lend further support to a growing link between autophagy and lipid metabolism, our findings are the first to suggest a possible molecular mechanism by which autophagy modulates organismal aging.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Autophagy*
  • Caenorhabditis elegans / cytology*
  • Caenorhabditis elegans / enzymology
  • Caenorhabditis elegans / physiology*
  • Caenorhabditis elegans Proteins / metabolism
  • Lipase / metabolism
  • Lipid Metabolism*
  • Longevity / physiology*
  • Models, Biological
  • Signal Transduction

Substances

  • Caenorhabditis elegans Proteins
  • LIPL-4 protein, C elegans
  • Lipase