The Exchangeable Apolipoprotein Nplp2 Sustains Lipid Flow and Heat Acclimation in Drosophila

Cell Rep. 2019 Apr 16;27(3):886-899.e6. doi: 10.1016/j.celrep.2019.03.074.

Abstract

In ectotherms, increased ambient temperature requires the organism to consume substantial amounts of energy to sustain a higher metabolic rate, prevent cellular damage, and respond to heat stress. Here, we identify a heat-inducible apolipoprotein required for thermal acclimation in Drosophila. Neuropeptide-like precursor 2 (Nplp2) is an abundant hemolymphatic protein thought to be a neuropeptide. In contrast, we show that Nplp2 contributes to lipid transport, functioning as an exchangeable apolipoprotein. More precisely, Nplp2-deficient flies accumulate lipids in their gut, have reduced fat stores, and display a dyslipoproteinemia, showing that Nplp2 is required for dietary lipid assimilation. Importantly, Nplp2 is induced upon thermal stress and contributes to survival upon heat stress. We propose that Nplp2 associates with lipoprotein particles under homeostatic and high energy-demand conditions to optimize fat transport and storage. Our study also shows that modulation of the lipid uptake and transport machinery is part of an integrated cytoprotective response.

Keywords: exchangeable lipoprotein; fat storage; heat acclimation; lipid transport; neuropeptide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acclimatization
  • Amino Acid Sequence
  • Animals
  • Apolipoproteins / chemistry
  • Apolipoproteins / genetics
  • Apolipoproteins / metabolism*
  • Drosophila / growth & development
  • Drosophila / metabolism*
  • Drosophila Proteins / chemistry
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Fat Body / metabolism
  • Fat Body / pathology
  • Heat-Shock Response
  • Intestinal Mucosa / metabolism
  • Larva / metabolism
  • Lipid Metabolism / physiology*
  • Lipoproteins / metabolism
  • Mutagenesis
  • Neuropeptides / chemistry
  • Neuropeptides / genetics
  • Neuropeptides / metabolism*
  • Protein Binding
  • Sequence Alignment
  • Temperature

Substances

  • Apolipoproteins
  • Drosophila Proteins
  • Lipoproteins
  • Neuropeptides
  • Nplp2 protein, Drosophila