Bile acids stimulate cholangiocyte fluid secretion by activation of transmembrane member 16A Cl - channels

Hepatology. 2018 Jul;68(1):187-199. doi: 10.1002/hep.29804. Epub 2018 May 9.


Bile acids stimulate a bicarbonate-rich choleresis, in part, through effects on cholangiocytes. Because Cl- channels in the apical membrane of cholangiocytes provide the driving force for secretion and transmembrane member 16A (TMEM16A) has been identified as the Ca2+ -activated Cl- channel in the apical membrane of cholangiocytes, the aim of the present study was to determine whether TMEM16A is the target of bile-acid-stimulated Cl- secretion and to identify the regulatory pathway involved. In these studies of mouse, rat, and human biliary epithelium exposure to ursodeoxycholic acid (UDCA) or tauroursodeoxycholic acid (TUDCA) rapidly increased the rate of exocytosis, ATP release, [Ca2+ ]i , membrane Cl- permeability, and transepithelial secretion. Bile-acid-stimulated Cl- currents demonstrated biophysical properties consistent with TMEM16A and were inhibited by pharmacological or molecular (small-interfering RNA; siRNA) inhibition of TMEM16A. Bile acid-stimulated Cl- currents were not observed in the presence of apyrase, suramin, or 2-aminoethoxydiphenyl borate (2-APB), demonstrating that current activation requires extracellular ATP, P2Y, and inositol 1,4,5-trisphosphate (IP3) receptors. TUDCA did not activate Cl- currents during pharmacologic inhibition of the apical Na+ -dependent bile acid transporter (ASBT), but direct intracellular delivery of TUDCA rapidly activated Cl- currents.

Conclusion: Bile acids stimulate Cl- secretion in mouse and human biliary cells through activation of membrane TMEM16A channels in a process regulated by extracellular ATP and [Ca2+ ]i . These studies suggest that TMEM16A channels may be targets to increase bile flow during cholestasis. (Hepatology 2018;68:187-199).

Publication types

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

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Anoctamin-1 / metabolism*
  • Bile Acids and Salts / physiology*
  • Bile Ducts / metabolism*
  • Calcium / metabolism
  • Chlorides / metabolism
  • Exocytosis
  • Humans
  • Inositol 1,4,5-Trisphosphate Receptors / metabolism
  • Mice
  • Organic Anion Transporters, Sodium-Dependent / metabolism
  • Primary Cell Culture
  • Rats
  • Receptors, Purinergic P2Y / metabolism
  • Secretory Pathway
  • Symporters / metabolism


  • Anoctamin-1
  • Bile Acids and Salts
  • Chlorides
  • Inositol 1,4,5-Trisphosphate Receptors
  • Organic Anion Transporters, Sodium-Dependent
  • Receptors, Purinergic P2Y
  • Symporters
  • sodium-bile acid cotransporter
  • Adenosine Triphosphate
  • Calcium