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Longer lifespan, altered metabolism, and stress resistance in Drosophila from ablation of cells making insulin-like ligands

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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  • Susan J Broughton
  • Matthew D W Piper
  • Tomoatsu Ikeya
  • Timothy M Bass
  • Jake Jacobson
  • Yasmine Driege
  • Pedro Martinez
  • Ernst Hafen
  • Dominic J Withers
  • Sally J Leevers
  • Linda Partridge
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<mark>Journal publication date</mark>22/02/2005
<mark>Journal</mark>Proceedings of the National Academy of Sciences of the United States of America
Issue number8
Volume102
Number of pages6
Pages (from-to)3105-3110
Publication StatusPublished
<mark>Original language</mark>English

Abstract

The insulin/insulin-like growth factor-like signaling pathway, present in all multicellular organisms, regulates diverse functions including growth, development, fecundity, metabolic homeostasis, and lifespan. In flies, ligands of the insulin/insulin-like growth factor-like signaling pathway, the Drosophila insulin-like peptides, regulate growth and hemolymph carbohydrate homeostasis during development and are expressed in a stage- and tissue-specific manner. Here, we show that ablation of Drosophila insulin-like peptide-producing median neurosecretory cells in the brain leads to increased fasting glucose levels in the hemolymph of adults similar to that found in diabetic mammals. They also exhibit increased storage of lipid and carbohydrate, reduced fecundity, and reduced tolerance of heat and cold. However, the ablated flies show an extension of median and maximal lifespan and increased resistance to oxidative stress and starvation.