Drosophila as a model for ageing

Biochim Biophys Acta Mol Basis Dis. 2018 Sep;1864(9 Pt A):2707-2717. doi: 10.1016/j.bbadis.2017.09.016. Epub 2017 Sep 28.

Abstract

Drosophila melanogaster has been a key model in developing our current understanding of the molecular mechanisms of ageing. Of particular note is its role in establishing the evolutionary conservation of reduced insulin and IGF-1-like signaling in promoting healthy ageing. Capitalizing on its many advantages for experimentation, more recent work has revealed how precise nutritional and genetic interventions can improve fly lifespan without obvious detrimental side effects. We give a brief summary of these recent findings as well as examples of how they may modify ageing via actions in the gut and muscle. These discoveries highlight how expanding our understanding of metabolic and signaling interconnections will provide even greater insight into how these benefits may be harnessed for anti-ageing interventions.

Keywords: Ageing; Dietary restriction; Drosophila; Insulin signaling; TOR; Tissue control of ageing.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Activating Transcription Factor 4 / metabolism
  • Aging / genetics
  • Aging / physiology*
  • Animals
  • Diet
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / physiology*
  • Gastrointestinal Tract / physiology
  • Genetic Engineering
  • Insulin / metabolism
  • Insulin-Like Growth Factor I / metabolism
  • Longevity / genetics
  • Longevity / physiology*
  • Metabolic Networks and Pathways / physiology
  • Models, Animal*
  • Muscles / physiology
  • Nutrition Assessment
  • Protein Kinases / metabolism
  • Research
  • Signal Transduction / physiology
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Drosophila Proteins
  • Insulin
  • Activating Transcription Factor 4
  • Insulin-Like Growth Factor I
  • GCN2 protein, Drosophila
  • Protein Kinases
  • TOR Serine-Threonine Kinases
  • AMP-Activated Protein Kinases