IL-33/ST2 plays a critical role in endothelial cell activation and microglia-mediated neuroinflammation modulation

J Neuroinflammation. 2018 May 4;15(1):136. doi: 10.1186/s12974-018-1169-6.

Abstract

Background: Interleukin-33 (IL-33) is increasingly being recognized as a key immunomodulatory cytokine in many neurological diseases.

Methods: In the present study, wild-type (WT) and IL-33-/- mice received intracerebroventricular (i.c.v.) injection of lipopolysaccharide (LPS) to induce neuroinflammation. Intravital microscopy was employed to examine leukocyte-endothelial interactions in the brain vasculature. The degree of neutrophil infiltration was determined by myeloperoxidase (MPO) staining. Real-time PCR and western blotting were used to detect endothelial activation. Enzyme-linked immunosorbent assay and quantitative PCR were conducted to detect pro-inflammatory cytokine levels in the brain.

Results: In IL-33-/- mice, neutrophil infiltration in the brain cortex and leukocyte-endothelial cell interactions in the cerebral microvessels were significantly decreased as compared to WT mice after LPS injection. In addition, IL-33-/- mice showed reduced activation of microglia and cerebral endothelial cells. In vitro results indicated that IL-33 directly activated cerebral endothelial cells and promoted pro-inflammatory cytokine production in LPS-stimulated microglia.

Conclusions: Our study indicated that IL-33/ST2 signaling plays an important role in the activation of microglia and cerebral endothelial cells and, therefore, is essential in leukocyte recruitment in brain inflammation. The role of IL-33/ST2 in LPS induced neuroinflammation.

Keywords: CNS inflammation; Endothelial activation; IL-33/ST2; Intravital microscopy; Microglia activation; Neutrophil infiltration.

MeSH terms

  • Animals
  • Animals, Newborn
  • Cells, Cultured
  • Encephalitis / chemically induced
  • Encephalitis / immunology
  • Encephalitis / metabolism*
  • Endothelial Cells / immunology
  • Endothelial Cells / metabolism*
  • Immunity, Innate / physiology
  • Injections, Intraventricular
  • Interleukin-1 Receptor-Like 1 Protein / biosynthesis*
  • Interleukin-1 Receptor-Like 1 Protein / immunology
  • Interleukin-33 / biosynthesis*
  • Interleukin-33 / immunology
  • Lipopolysaccharides / toxicity
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microglia / immunology
  • Microglia / metabolism*
  • Neutrophil Infiltration / physiology

Substances

  • Il1rl1 protein, mouse
  • Il33 protein, mouse
  • Interleukin-1 Receptor-Like 1 Protein
  • Interleukin-33
  • Lipopolysaccharides