Activated FOXO-mediated insulin resistance is blocked by reduction of TOR activity

Cell Metab. 2006 Aug;4(2):133-42. doi: 10.1016/j.cmet.2006.05.013.

Abstract

Reducing insulin/IGF signaling allows for organismal survival during periods of inhospitable conditions by regulating the diapause state, whereby the organism stockpiles lipids, reduces fertility, increases stress resistance, and has an increased lifespan. The Target of Rapamycin (TOR) responds to changes in growth factors, amino acids, oxygen tension, and energy status; however, it is unclear how TOR contributes to physiological homeostasis and disease conditions. Here, we show that reducing the function of Drosophila TOR results in decreased lipid stores and glucose levels. Importantly, this reduction of dTOR activity blocks the insulin resistance and metabolic syndrome phenotypes associated with increased activity of the insulin responsive transcription factor, dFOXO. Reduction in dTOR function also protects against age-dependent decline in heart function and increases longevity. Thus, the regulation of dTOR activity may be an ancient "systems biological" means of regulating metabolism and senescence, that has important evolutionary, physiological, and clinical implications.

Publication types

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

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Animals
  • Down-Regulation
  • Drosophila
  • Drosophila Proteins / antagonists & inhibitors
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila Proteins / pharmacology
  • Forkhead Transcription Factors / antagonists & inhibitors
  • Forkhead Transcription Factors / metabolism*
  • Glucose / analysis
  • Insulin Resistance / physiology*
  • Lipids / analysis
  • Models, Biological
  • Molecular Sequence Data
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphatidylinositol 3-Kinases / pharmacology
  • Protein Kinases
  • Sequence Alignment
  • Signal Transduction
  • TOR Serine-Threonine Kinases
  • Up-Regulation

Substances

  • Drosophila Proteins
  • FOXO protein, Drosophila
  • Forkhead Transcription Factors
  • Lipids
  • Protein Kinases
  • target of rapamycin protein, Drosophila
  • TOR Serine-Threonine Kinases
  • Glucose