Pleiotropic functions of TNF-α in the regulation of the intestinal epithelial response to inflammation

Int Immunol. 2014 Sep;26(9):509-15. doi: 10.1093/intimm/dxu051. Epub 2014 May 12.

Abstract

An important function of intestinal epithelial cells (IECs) is to maintain the integrity of the mucosal barrier. Inflammation challenges the integrity of the mucosal barrier and the intestinal epithelium needs to adapt to a multitude of signals in order to perform the complex process of maintenance and restitution of its barrier function. Dysfunctions in epithelial barrier integrity and restoration contribute to the pathogenesis of inflammatory bowel diseases (IBDs) such as Crohn's disease and ulcerative colitis. Mucosal healing has developed to a significant treatment goal in IBD. In this review, we would like to highlight physiologic and pathologic adaptations of the intestinal epithelium to inflammation, exemplified by its responses to TNF-α. A large body of literature exists that highlights the diverse effects of this cytokine on IECs. TNF-α modulates intestinal mucus secretion and constitution. TNF-α stimulation modulates paracellular flow via tight junctional control. TNF-α induces intracellular signaling cascades that determine significant cell fate decisions such as survival, cell death or proliferation. TNF-α impacts epithelial wound healing in ErbB- and Wnt-dependent pathways while also importantly guiding immune cell attraction and function. We selected important studies from recent years with a focus on functional in vivo data providing crucial insights into the complex process of intestinal homeostasis.

Keywords: intestinal epithelium; mucosal immunology; tumor necrosis factor.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • ErbB Receptors / immunology
  • Humans
  • Immunity, Mucosal*
  • Inflammation / immunology
  • Inflammation / pathology
  • Inflammatory Bowel Diseases / immunology*
  • Inflammatory Bowel Diseases / pathology
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / pathology
  • Tumor Necrosis Factor-alpha / immunology*
  • Wnt Proteins / immunology
  • Wnt Signaling Pathway / immunology*

Substances

  • TNF protein, human
  • Tumor Necrosis Factor-alpha
  • Wnt Proteins
  • EGFR protein, human
  • ErbB Receptors