Extracellular matrix protein lumican regulates inflammation in a mouse model of colitis

Kristin Lohr, Hardik Sardana, Seakwoo Lee, Feng Wu, David L. Huso, Abdel Rahim Hamad, Shukti Chakravarti

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Abnormal innate immune response contributes to inflammatory bowel disease (IBD) and experimental mouse colitis. Colitis studies have focused primarily on key regulators of innate immunity, like pathogen recognition receptors and cytoplasmic mediators. Extracellular matrix (ECM) proteins are emerging as modulators of inflammatory responses by virtue of their interactions with pathogen-associated molecular patterns (PAMPs), cytokines, growth factors, receptors, and ECM fragments that mimic pathogens or cytokines. The ECM proteins have not been investigated in IBD at great depth from this standpoint. We have shown previously that the ECM protein lumican modulates host sensing of bacterial lipopolysaccharides (LPS) by Toll-like receptor (TLR) 4, and neutrophil chemotaxis via integrins. Methods: Here we investigated the role of lumican in the development of colitis mediated by intrarectal administration of the hapten 2-4-5, trinitrobenzene sulfonic acid (TNBS) in Lum +/+ and Lum -/- mice. Results: The TNBS treated Lum +/+ mouse colons showed marked increases in CXCL1, tumor necrosis factor alpha (TNF-α), and neutrophil infiltration, whereas these responses were significantly dampened in the Lum -/- mice. The nuclear factor kappa B (NF-κB) transcription factor, known to regulate inflammatory genes, showed a robust increase after TNBS treatment in Lum +/+ but not in Lum -/- colons. Also, nuclear translocation of NF-κB was delayed in LPS stimulated Lum -/- primary peritoneal macrophages. Conclusions: The Lum -/- mice have low innate immune and inflammatory responses, but more severe body weight loss and tissue damage, a phenomenon seen in the innate immune impaired Tlr4 -/- and MyD88 -/- mice. Therefore, lumican promotes intestinal homeostasis by aiding innate immune and inflammatory responses that are beneficial in the early stages of colitis.

Original languageEnglish (US)
Pages (from-to)143-151
Number of pages9
JournalInflammatory bowel diseases
Volume18
Issue number1
DOIs
StatePublished - Jan 2012

Keywords

  • CD14
  • TLR4
  • dextran sodium sulfate
  • extracellular matrix
  • inflammation
  • innate immune response
  • lumican
  • murine colitis
  • neutrophils
  • tri-nitrobenzene sulfonic acid

ASJC Scopus subject areas

  • Immunology and Allergy
  • Gastroenterology

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