Neutrophil Extracellular Traps Sustain Inflammatory Signals in Ulcerative Colitis

J Crohns Colitis. 2019 May 27;13(6):772-784. doi: 10.1093/ecco-jcc/jjy215.

Abstract

Background and aims: In ulcerative colitis [UC], mucosal damage occurs in areas that are infiltrated with neutrophils. The antimicrobial function of neutrophils relies in part on the formation of extracellular web-like structures, named neutrophil extracellular traps [NETs]. The formation and/or clearance of aberrant NETs have been associated with several immune diseases. Here we investigated the role of NETs in UC-related inflammation.

Methods: The expression of NET-associated proteins was evaluated in colonic biopsies of patients with Crohn's disease [CD], UC and in normal controls [NC] by Western blotting, immunofluorescence and immunohistochemistry. Colonic biopsies of UC patients were analysed before and after anti-tumour necrosis factor α [anti-TNF-α] treatment. The capacity of neutrophils to produce NETs upon activation was tested in vitro. UC lamina propria mononuclear cells [LPMCs] were cultured with NETs in the presence or absence of an extracellular signal-regulated kinase-1/2 [ERK1/2] inhibitor and inflammatory cytokine induction was assessed by real-time polymerase chain reaction and enzyme-linked immunosorbent assay. We also characterized the contribution of NETs in dextran sodium sulfate [DSS]-induced colitis.

Results: NET-associated proteins were over-expressed in inflamed colon of UC patients as compared to CD patients and NC. Circulating neutrophils of UC patients produced NETs in response to TNF-α stimulation, and reduced expression of NET-related proteins and diminished NET formation were seen in patients receiving successful treatment with anti-TNF-α. Treatment of UC LPMCs with NETs activated ERK1/2, thus enhancing TNF-α and interleukin-1β [IL-1β] production. NETs were induced in mice with DSS-colitis and in vivo inhibition of NET release attenuated colitis.

Conclusions: Our data show that NET release occurs in UC and suggest a role for NETs in sustaining mucosal inflammation in this disorder.

Keywords: NETosis; PAD4; inflammatory bowel disease; neutrophils; ulcerative colitis.

MeSH terms

  • Animals
  • Colitis, Ulcerative / metabolism*
  • Colitis, Ulcerative / pathology
  • Colon / metabolism
  • Colon / pathology
  • Disease Models, Animal
  • Extracellular Traps / metabolism*
  • Female
  • Fluorescent Antibody Technique
  • Humans
  • Inflammation / metabolism*
  • Inflammation / pathology
  • Interleukin-1beta / metabolism
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • MAP Kinase Signaling System
  • Mice
  • Mice, Inbred BALB C
  • Real-Time Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-1beta
  • Tumor Necrosis Factor-alpha