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. (Inflamm Bowel Dis 2011;)
1 Gastroenterology Division, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland
2 All India Institute of Medical Sciences, New Delhi, India
3 Section of Gastroenterology, Department of Medicine, University of Chicago, Chicago, Illinois
4 Department of Comparative Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland
5 Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland
* Department of Medicine, Johns Hopkins University, Ross 935, 720 Rutland Ave., Baltimore, MD 21205
Received 22 February 2011; Accepted 25 February 2011
Published online 11 April 2011 in Wiley Online Library (wileyonlinelibrary.com).
Supported by Crohn's and Colitis Foundation of America Senior Investigator Award and NEI/NIH EY 11654 (to S.C.).