Intraperitoneal influx of neutrophils in response to IL-33 is mast cell-dependent

Blood. 2013 Jan 17;121(3):530-6. doi: 10.1182/blood-2012-05-434209. Epub 2012 Oct 23.

Abstract

IL-33 is a recently discovered cytokine involved in induction of Th2 responses and functions as an alarmin. Despite numerous recent studies targeting IL-33, its role in vivo is incompletely understood. Here we investigated inflammatory responses to intraperitoneal IL-33 injections in wild-type and mast cell-deficient mice. We found that wild-type mice, but not mast cell-deficient W(sh)/W(sh) mice, respond to IL-33 treatment with neutrophil infiltration to the peritoneum, whereas other investigated cell types remained unchanged. In W(sh)/W(sh) mice, the IL-33-induced innate neutrophil response could be rescued by local reconstitution with wild-type but not with T1/ST2(-/-) mast cells, demonstrating a mast cell-dependent mechanism. Furthermore, we found this mechanism to be partially dependent on mast cell-derived TNF, as we observed reduced neutrophil infiltration in W(sh)/W(sh) mice reconstituted with TNF(-/-) bone marrow-derived mast cells compared with those reconstituted with wild-type bone marrow-derived mast cells. In agreement with our in vivo findings, we demonstrate that human neutrophils migrate toward the supernatant of IL-33-treated human mast cells. Taken together, our findings reveal that IL-33 activates mast cells in vivo to recruit neutrophils, a mechanism dependent on IL-33R expression on peritoneal mast cells. Mast cells activated in vivo by IL-33 probably play an important role in inflammatory reactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Cells
  • Cell Communication / drug effects
  • Cell Communication / immunology*
  • Cell Movement / drug effects
  • Cell Movement / immunology
  • Cells, Cultured
  • Fetal Blood / cytology
  • Humans
  • Injections, Intraperitoneal
  • Interleukin-1 Receptor-Like 1 Protein
  • Interleukin-33
  • Interleukins / immunology*
  • Interleukins / metabolism
  • Interleukins / pharmacology
  • Mast Cells / cytology*
  • Mast Cells / drug effects
  • Mast Cells / immunology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neutrophils / cytology*
  • Neutrophils / drug effects
  • Neutrophils / immunology
  • Peritoneal Cavity / cytology
  • Proto-Oncogene Proteins c-kit / metabolism
  • Receptors, Cell Surface / metabolism
  • Receptors, Interleukin / metabolism

Substances

  • IL1RL1 protein, human
  • IL33 protein, human
  • Il1rl1 protein, mouse
  • Il33 protein, mouse
  • Interleukin-1 Receptor-Like 1 Protein
  • Interleukin-33
  • Interleukins
  • Receptors, Cell Surface
  • Receptors, Interleukin
  • Proto-Oncogene Proteins c-kit