Innate immune receptor NOD2 mediates LGR5+ intestinal stem cell protection against ROS cytotoxicity via mitophagy stimulation

Proc Natl Acad Sci U S A. 2020 Jan 28;117(4):1994-2003. doi: 10.1073/pnas.1902788117. Epub 2020 Jan 9.

Abstract

The nucleotide-binding oligomerization domain-containing protein 2 (NOD2) agonist muramyl dipeptide (MDP), a peptidoglycan motif common to all bacteria, supports leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5)+ intestinal stem cell (ISC) survival through NOD2 activation upon an otherwise lethal oxidative stress-mediated signal. However, the underlying protective mechanisms remain unknown. Here, using irradiation as stressor and primarily murine-derived intestinal organoids as a model system, we show that MDP induced a significant reduction of total and mitochondrial reactive oxygen species (ROS) within ISCs, which was associated with mitophagy induction. ATG16L1 knockout (KO) and NOD2 KO organoids did not benefit from the MDP-induced cytoprotection. We confirmed the MDP-dependent induction of ISC mitophagy upon stress in vivo. These findings elucidate the NOD2-mediated mechanism of cytoprotection involving the clearance of the lethal excess of ROS molecules through mitophagy, triggered by the coordinated activation of NOD2 and ATG16L1 by a nuclear factor κB (NF-κB)-independent pathway.

Keywords: LGR5 intestinal stem cells; NOD2; ROS; autophagy; muramyl dipeptide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylmuramyl-Alanyl-Isoglutamine / pharmacology*
  • Animals
  • Cells, Cultured
  • Cytoprotection*
  • Immunity, Innate / drug effects
  • Immunity, Innate / immunology
  • Immunity, Innate / radiation effects
  • Intestines / drug effects
  • Intestines / growth & development*
  • Intestines / radiation effects
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Mitophagy / drug effects*
  • Mitophagy / radiation effects
  • Nod2 Signaling Adaptor Protein / genetics
  • Nod2 Signaling Adaptor Protein / metabolism*
  • Oxidative Stress / drug effects
  • Reactive Oxygen Species*
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Signal Transduction
  • Stem Cells / cytology*
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Stem Cells / radiation effects

Substances

  • Lgr5 protein, mouse
  • Nod2 Signaling Adaptor Protein
  • Nod2 protein, mouse
  • Reactive Oxygen Species
  • Receptors, G-Protein-Coupled
  • Acetylmuramyl-Alanyl-Isoglutamine

Associated data

  • figshare/10.6084/m9.figshare.11536920