Regulation of mucin secretion in human gallbladder epithelial cells: predominant role of calcium and protein kinase C

Gastroenterology. 1997 Mar;112(3):978-90. doi: 10.1053/gast.1997.v112.pm9041261.

Abstract

Background & aims: The cellular mechanisms that regulate biliary mucin secretion in humans are unknown. To address this question, human gallbladder epithelial cells were used in primary culture.

Methods: [1-(14)C]-glucosamine-labeled glycoproteins secreted in vitro were analyzed and quantified after exposing cells to activators and inhibitors of the main transduction pathways and to potential biologically active secretagogues.

Results: Secreted glycoproteins showed characteristics of biliary mucins. Activators of adenosine 3',5'-cyclic monophosphate-dependent pathway as well as secretin and vasoactive intestinal polypeptide did not significantly modify mucin secretion. By contrast, ionomycin and phorbol-12-myristate 13-acetate increased mucin secretion by 292% +/- 48% and 134% +/- 19% over basal level, respectively. The effects of these two agents were additive and were mediated by a calcium-dependent pathway implicating Ca2+/calmodulin-dependent protein kinase II (Ca2+/CaM-kinase II) and by the activation of protein kinase C (PKC), respectively, as ascertained by using inhibitors. Mucin secretion was stimulated by extracellular adenosine 5'-triphosphate via P2U receptors, cytosolic calcium increase, and PKC and by taurochenodeoxycholate via cytosolic calcium increase and Ca2+/CaM-kinase II.

Conclusions: Mucin secretion in human gallbladder is regulated predominantly by calcium-dependent pathways implicating Ca2+/CaM-kinase II and PKC. Extracellular adenosine 5'-triphosphate and taurochenodeoxycholate may play a role in the regulation of biliary mucin secretion by activating these different signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Calcium / physiology*
  • Cells, Cultured
  • Egtazic Acid / pharmacology
  • Epithelium / metabolism
  • Gallbladder / metabolism*
  • Humans
  • Mucins / metabolism*
  • Protein Kinase C / physiology*
  • Signal Transduction
  • Taurochenodeoxycholic Acid / pharmacology
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Mucins
  • Taurochenodeoxycholic Acid
  • Egtazic Acid
  • Adenosine Triphosphate
  • Protein Kinase C
  • Tetradecanoylphorbol Acetate
  • Calcium