Bile salts regulate intestinal epithelial cell migration by nuclear factor-kappa B-induced expression of transforming growth factor-beta

J Am Coll Surg. 2003 Dec;197(6):974-84. doi: 10.1016/S1072-7515(03)00720-8.

Abstract

Background: Mucosal restitution is an important repair modality in the gastrointestinal tract. We have shown that taurodeoxycholate increases intestinal epithelial cell migration by increasing TGF-beta expression, and that the transcription factor NF-kappa B regulates TDCA induced cell migration after injury. The objectives of this study were to determine if this is a property shared by other bile salts or an effect specific to TDCA, and to determine if NF-kappa B regulates TGF-beta expression.

Study design: Studies were conducted in IEC-6 cells. Cell migration was examined using an in vitro model. TGF-beta protein and mRNA expression was determined by ELISA and Northern blot analysis. Sequence-specific NF-kappa B binding activity was measured by gel shift assays.

Results: Taurocholate and deoxycholate at physiologic concentrations significantly increased intestinal epithelial cell migration 6 hours after wounding (p < 0.01), and was associated with a significant increase in specific NF-kappa B binding activity. Inhibition of NF-kappa B activity significantly inhibited cell migration during restitution and resulted in a significant decrease in TGF-beta mRNA expression and protein expression.

Conclusions: We conclude that bile salts at physiologic conditions increase cell migration after injury, an effect regulated by NF-kappa B. Further, NF-kappa B elicits TGF-beta gene transcription during cell migration. These data support a physiologic role of bile salts in the maintenance of intestinal mucosal integrity.

MeSH terms

  • Animals
  • Cell Line
  • Cell Movement / physiology*
  • Deoxycholic Acid / physiology*
  • Gene Expression Regulation / genetics
  • Intestinal Mucosa / pathology
  • Intestinal Mucosa / physiology*
  • NF-kappa B / physiology*
  • Rats
  • Taurocholic Acid / physiology*
  • Transforming Growth Factor beta / genetics*

Substances

  • NF-kappa B
  • Transforming Growth Factor beta
  • Deoxycholic Acid
  • Taurocholic Acid