Oxidative stress induces stem cell proliferation via TRPA1/RyR-mediated Ca2+ signaling in the Drosophila midgut

Elife. 2017 May 31:6:e22441. doi: 10.7554/eLife.22441.

Abstract

Precise regulation of stem cell activity is crucial for tissue homeostasis and necessary to prevent overproliferation. In the Drosophila adult gut, high levels of reactive oxygen species (ROS) has been detected with different types of tissue damage, and oxidative stress has been shown to be both necessary and sufficient to trigger intestinal stem cell (ISC) proliferation. However, the connection between oxidative stress and mitogenic signals remains obscure. In a screen for genes required for ISC proliferation in response to oxidative stress, we identified two regulators of cytosolic Ca2+ levels, transient receptor potential A1 (TRPA1) and ryanodine receptor (RyR). Characterization of TRPA1 and RyR demonstrates that Ca2+ signaling is required for oxidative stress-induced activation of the Ras/MAPK pathway, which in turns drives ISC proliferation. Our findings provide a link between redox regulation and Ca2+ signaling and reveal a novel mechanism by which ISCs detect stress signals.

Keywords: D. melanogaster; Ras/MAPK; calcium; cation channels; cell biology; developmental biology; redox; stem cell; stem cells; tissue homeostasis.

MeSH terms

  • Animals
  • Cell Proliferation*
  • Drosophila / physiology*
  • Drosophila Proteins / metabolism*
  • Gastrointestinal Tract / physiology
  • Ion Channels
  • Oxidative Stress*
  • Ryanodine Receptor Calcium Release Channel / metabolism*
  • Signal Transduction
  • Stem Cells / physiology*
  • TRPA1 Cation Channel / metabolism*

Substances

  • Drosophila Proteins
  • Ion Channels
  • Ryanodine Receptor Calcium Release Channel
  • TRPA1 Cation Channel
  • TrpA1 protein, Drosophila