NF-kappaB regulates intestinal epithelial cell and bile salt-induced migration after injury

Ann Surg. 2003 Apr;237(4):494-501. doi: 10.1097/01.SLA.0000060459.03270.E7.

Abstract

Objective: To determine if NF-kappa B regulates intestinal epithelial cell migration and if it has a role during bile salt-induced migration.

Summary background data: Mucosal restitution is an important repair modality in the gastrointestinal tract. The authors have shown that taurodeoxycholate (TDCA) increases intestinal epithelial cell migration. NF-kappa B regulates activation of a number of genes involved in inflammatory responses.

Methods: Studies were conducted in IEC-6 cells. I kappa B protein expression was determined by Western blot analysis. Sequence-specific NF-kappa B binding activity was measured by EMSA shift assays and nuclear localization by immunohistochemistry. Cell migration was examined by using an in vitro model that mimics the early cell division-independent stages of epithelial restitution.

Results: The process of cell migration over the wounded area was associated with a significant increase in NF-kappa B binding activity in IEC-6 cells. Immunohistochemistry revealed translocation of NF-kappa B into the nucleus. Western blot analysis showed that injury decreased I kappa B protein expression. Inhibition of the binding activity by treatment with a specific NF-kappa B inhibitor, MG-132, inhibited cell migration during restitution. Further, exposure to TDCA at the physiologic concentration that induces intestinal epithelial cell migration increased NF-kappa B binding activity, induced NF-kappa B translocation into the nucleus, and decreased I kappa B protein expression. MG-132 also inhibits bile salt-induced cell migration.

Conclusions: NF-kappa B regulates intestinal epithelial cell migration. Bile salts at physiologic concentrations increase cell migration by activation of NF-kappa B. These data show that bile salts may have a role in the maintenance of intestinal mucosal integrity.

MeSH terms

  • Animals
  • Bile Acids and Salts
  • Cell Movement / drug effects
  • Cell Movement / physiology*
  • Cells, Cultured
  • Intestinal Mucosa / cytology*
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / injuries
  • Leupeptins / pharmacology
  • NF-kappa B / biosynthesis
  • NF-kappa B / physiology*
  • Rats
  • Taurodeoxycholic Acid / pharmacology

Substances

  • Bile Acids and Salts
  • Leupeptins
  • NF-kappa B
  • Taurodeoxycholic Acid
  • benzyloxycarbonylleucyl-leucyl-leucine aldehyde