Adipose Dicer-1 modulates systemic insulin signaling and longevity via a miR-8-Aop-Dilp6 axis

Proc Natl Acad Sci U S A. 2026 Mar 31;123(13):e2525327123. doi: 10.1073/pnas.2525327123. Epub 2026 Mar 24.

Abstract

Interorgan communication is essential for metabolic homeostasis and healthy aging, with adipose tissue acting as a central hub that coordinates systemic metabolism, stress responses, and longevity. Here, we show that the miRNA-processing enzyme Dicer-1 (Dcr-1) acts in the fat body (FB) to regulate Dilp2 secretion from brain insulin-producing cells (IPCs), thereby modulating systemic insulin signaling and lifespan in Drosophila. Dcr-1 expression is reduced in multiple long-lived conditions, and its partial downregulation enhances oxidative stress resistance, alters lipid metabolism, and extends lifespan even under dietary restriction. Proteomic profiling of FBs from Dcr-1 heterozygous flies revealed widespread metabolic reprogramming and stress adaptation consistent with attenuated insulin/IGF signaling (IIS). Mechanistically, reduced Dcr-1 lowers miR-8 levels in the FB, which indirectly upregulates Drosophila insulin-like peptide 6 (Dilp6). Dilp6 acts nonautonomously to suppress Dilp2 secretion from IPCs, reducing systemic IIS and promoting longevity. We further show that Dcr-1 reduction activates the ETS-family repressor Aop/ETV6 downstream of Ras-Erk signaling, which is required for Dilp6 induction and the lifespan extension observed upon miR-8 depletion. Collectively, these findings reveal a miRNA-dependent regulatory axis that couples adipose-derived endocrine signals to systemic insulin regulation and aging, positioning Dcr-1 as a central node in the control of metabolic homeostasis and lifespan.

Keywords: adipose tissue; insulin like peptides; inter organ communication; miRNA; oxidative stress.

MeSH terms

  • Animals
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / metabolism
  • Fat Body / metabolism
  • Insulin* / metabolism
  • Insulin-Like Peptides* / genetics
  • Insulin-Like Peptides* / metabolism
  • Longevity* / physiology
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Oxidative Stress
  • RNA Helicases* / genetics
  • RNA Helicases* / metabolism
  • Ribonuclease III* / genetics
  • Ribonuclease III* / metabolism
  • Signal Transduction
  • Somatomedins

Substances

  • MicroRNAs
  • Drosophila Proteins
  • Insulin
  • Ribonuclease III
  • Dcr-1 protein, Drosophila
  • RNA Helicases
  • MIRN8 microRNA, Drosophila
  • Insulin-Like Peptides
  • Ilp6 protein, Drosophila
  • Somatomedins

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