Phosphatidylinositol 3-kinase facilitates bile acid-induced Ca(2+) responses in pancreatic acinar cells

Am J Physiol Gastrointest Liver Physiol. 2007 Mar;292(3):G875-86. doi: 10.1152/ajpgi.00558.2005. Epub 2006 Dec 7.

Abstract

Bile acids are known to induce Ca(2+) signals in pancreatic acinar cells. We have recently shown that phosphatidylinositol 3-kinase (PI3K) regulates changes in free cytosolic Ca(2+) concentration ([Ca(2+)](i)) elicited by CCK by inhibiting sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA). The present study sought to determine whether PI3K regulates bile acid-induced [Ca(2+)](i) responses. In pancreatic acinar cells, pharmacological inhibition of PI3K with LY-294002 or wortmannin inhibited [Ca(2+)](i) responses to taurolithocholic acid 3-sulfate (TLC-S) and taurochenodeoxycholate (TCDC). Furthermore, genetic deletion of the PI3K gamma-isoform also decreased [Ca(2+)](i) responses to bile acids. Depletion of CCK-sensitive intracellular Ca(2+) pools or application of caffeine inhibited bile acid-induced [Ca(2+)](i) signals, indicating that bile acids release Ca(2+) from agonist-sensitive endoplasmic reticulum (ER) stores via an inositol (1,4,5)-trisphosphate-dependent mechanism. PI3K inhibitors increased the amount of Ca(2+) in intracellular stores during the exposure of acinar cells to bile acids, suggesting that PI3K negatively regulates SERCA-dependent Ca(2+) reloading into the ER. Bile acids inhibited Ca(2+) reloading into ER in permeabilized acinar cells. This effect was augmented by phosphatidylinositol (3,4,5)-trisphosphate (PIP(3)), suggesting that both bile acids and PI3K act synergistically to inhibit SERCA. Furthermore, inhibition of PI3K by LY-294002 completely inhibited trypsinogen activation caused by the bile acid TLC-S. Our results indicate that PI3K and its product, PIP(3), facilitate bile acid-induced [Ca(2+)](i) responses in pancreatic acinar cells through inhibition of SERCA-dependent Ca(2+) reloading into the ER and that bile acid-induced trypsinogen activation is mediated by PI3K. The findings have important implications for the mechanism of acute pancreatitis since [Ca(2+)](i) increases and trypsinogen activation mediate key pathological processes in this disorder.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Androstadienes / pharmacology
  • Animals
  • Bile Acids and Salts / pharmacology*
  • Calcium / metabolism*
  • Cells, Cultured
  • Cholecystokinin / pharmacology
  • Chromones / pharmacology
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Inositol 1,4,5-Trisphosphate Receptors / antagonists & inhibitors
  • Ionomycin / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Morpholines / pharmacology
  • Pancreas, Exocrine / cytology
  • Pancreas, Exocrine / drug effects*
  • Pancreas, Exocrine / metabolism
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphoinositide-3 Kinase Inhibitors
  • Phosphorylation / drug effects
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / antagonists & inhibitors
  • Taurochenodeoxycholic Acid / pharmacology
  • Taurolithocholic Acid / analogs & derivatives
  • Taurolithocholic Acid / pharmacology
  • Thapsigargin / pharmacology
  • Wortmannin

Substances

  • Androstadienes
  • Bile Acids and Salts
  • Chromones
  • Enzyme Inhibitors
  • Inositol 1,4,5-Trisphosphate Receptors
  • Morpholines
  • Phosphoinositide-3 Kinase Inhibitors
  • taurolithocholic acid 3-sulfate
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Taurochenodeoxycholic Acid
  • Taurolithocholic Acid
  • Ionomycin
  • Thapsigargin
  • Cholecystokinin
  • Proto-Oncogene Proteins c-akt
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases
  • Calcium
  • Wortmannin