Mucin secretion by the human colon cell line LS174T is regulated by bile salts

Glycobiology. 1999 Jan;9(1):13-9. doi: 10.1093/glycob/9.1.13.

Abstract

We recently reported that bile salts play a role in the regulation of mucin secretion by cultured dog gallbladder epithelial cells. In this study we have examined whether bile salts also influence mucin secretion by the human epithelial colon cell line LS174T. Solutions of bile salts were applied to monolayers of LS174T cells. Mucin secretion was quantified by measuring the secretion of [3H]GlcNAc labeled glycoproteins. Both unconjugated bile salts as well as taurine conjugated bile salts stimulated mucin secretion by the colon cells in a dose-dependent fashion. Hydrophobic bile salts were more potent stimulators than hydrophilic bile salts. Free (unconjugated) bile salts were more stimulatory compared with their taurine conjugated counterparts. Stimulation of mucin secretion by LS174T cells was found to occur at much lower bile salt concentrations than in the experiments with the dog gallbladder epithelial cells. The protein kinase C activators PMA and PDB had no stimulatory effect on mucin secretion. We conclude that mucin secretion by the human colon epithelial cell line LS174T is regulated by bile salts. We suggest that regulation of mucin secretion by bile salts might be a common mechanism, by which different epithelia protect themselves against the detergent action of bile salts, to which they are exposed throughout the gastrointestinal tract.

Publication types

  • Comparative Study

MeSH terms

  • Adenocarcinoma
  • Animals
  • Bile Acids and Salts / chemistry
  • Bile Acids and Salts / pharmacology*
  • Colon / drug effects
  • Colon / metabolism*
  • Colonic Neoplasms
  • Dogs
  • Enzyme Activation / drug effects
  • Epithelium / metabolism
  • Humans
  • Mucins / metabolism*
  • Phorbol 12,13-Dibutyrate / pharmacology
  • Protein Kinase C / metabolism
  • Solutions
  • Structure-Activity Relationship
  • Taurochenodeoxycholic Acid / pharmacology
  • Tetradecanoylphorbol Acetate / pharmacology
  • Tritium
  • Tumor Cells, Cultured

Substances

  • Bile Acids and Salts
  • Mucins
  • Solutions
  • Tritium
  • Phorbol 12,13-Dibutyrate
  • Taurochenodeoxycholic Acid
  • ursodoxicoltaurine
  • Protein Kinase C
  • Tetradecanoylphorbol Acetate