Oxidant Sensing by TRPM2 Inhibits Neutrophil Migration and Mitigates Inflammation

Dev Cell. 2016 Sep 12;38(5):453-62. doi: 10.1016/j.devcel.2016.07.014. Epub 2016 Aug 25.

Abstract

Blood neutrophils perform an essential host-defense function by directly migrating to bacterial invasion sites to kill bacteria. The mechanisms mediating the transition from the migratory to bactericidal phenotype remain elusive. Here, we demonstrate that TRPM2, a trp superfamily member, senses neutrophil-generated reactive oxygen species and restrains neutrophil migration. The inhibitory function of oxidant sensing by TRPM2 requires the oxidation of Cys549, which then induces TRMP2 binding to formyl peptide receptor 1 (FPR1) and subsequent FPR1 internalization and signaling inhibition. The oxidant sensing-induced termination of neutrophil migration at the site of infection permits a smooth transition to the subsequent microbial killing phase.

MeSH terms

  • Animals
  • Cell Movement / genetics
  • HL-60 Cells
  • Humans
  • Inflammation / drug therapy
  • Inflammation / genetics*
  • Inflammation / pathology
  • Lung / enzymology
  • Mice
  • Neutrophils / metabolism
  • Oxidants / metabolism
  • Peroxidase / metabolism
  • Reactive Oxygen Species / metabolism*
  • Receptors, Formyl Peptide / genetics
  • Receptors, Formyl Peptide / metabolism*
  • TRPM Cation Channels / genetics
  • TRPM Cation Channels / metabolism*

Substances

  • FPR1 protein, human
  • Oxidants
  • Reactive Oxygen Species
  • Receptors, Formyl Peptide
  • TRPM Cation Channels
  • TRPM2 protein, human
  • Peroxidase