HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text Full Text (PDF) All Versions of this Article: 295/4/G725    most recent ajpgi.90265.2008v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Web of Science (7) Citing Articles via Google Scholar Google Scholar Articles by Masyuk, A. I. Articles by LaRusso, N. F. Search for Related Content PubMed PubMed Citation Articles by Masyuk, A. I. Articles by LaRusso, N. F.

LIVER AND BILIARY TRACT

Cholangiocyte primary cilia are chemosensory organelles that detect biliary nucleotides via P2Y₁₂ purinergic receptors

¹Mayo Clinic College of Medicine, Department of Internal Medicine, Rochester, Minnesota; ²Laboratory of Molecular Genetics, Division of Gene Therapy and Hepatology, University of Navarra School of Medicine, Clínica Universitaria and Centro de Investigación Médica Aplicada (CIMA), Centro de Investigación Biomédica en Red: Enfermedades Hepáticas y Digestivas (CIBERehd), Pamplona, Spain; ³Chonbuk National University Medical School, Jeonju, Jeonbuk, Republic of Korea

Submitted 28 March 2008 ; accepted in final form 5 August 2008

Cholangiocytes, the epithelial cells lining intrahepatic bile ducts, contain primary cilia, which are mechano- and osmosensory organelles detecting changes in bile flow and osmolality and transducing them into intracellular signals. Here, we asked whether cholangiocyte cilia are chemosensory organelles by testing the expression of P2Y purinergic receptors and components of the cAMP signaling cascade in cilia and their involvement in nucleotide-induced cAMP signaling in the cells. We found that P2Y₁₂ purinergic receptor, adenylyl cyclases (i.e., AC4, AC6, and AC8), and protein kinase A (i.e., PKA RI-β and PKA RII- regulatory subunits), exchange protein directly activated by cAMP (EPAC) isoform 2, and A-kinase anchoring proteins (i.e., AKAP150) are expressed in cholangiocyte cilia. ADP, an endogenous agonist of P2Y₁₂ receptors, perfused through the lumen of isolated rat intrahepatic bile ducts or applied to the ciliated apical surface of normal rat cholangiocytes (NRCs) in culture induced a 1.9- and 1.5-fold decrease of forskolin-induced cAMP levels, respectively. In NRCs, the forskolin-induced cAMP increase was also lowered by 1.3-fold in response to ATP-S, a nonhydrolyzed analog of ATP but was not affected by UTP. The ADP-induced changes in cAMP levels in cholangiocytes were abolished by chloral hydrate (a reagent that removes cilia) and by P2Y₁₂ siRNAs, suggesting that cilia and ciliary P2Y₁₂ are involved in nucleotide-induced cAMP signaling. In conclusion, cholangiocyte cilia are chemosensory organelles that detect biliary nucleotides through ciliary P2Y₁₂ receptors and transduce corresponding signals into a cAMP response.

liver; ADP; adenylyl cyclases; cAMP; protein kinase A; exchange protein directly activated by cAMP; A-kinase anchoring protein 150

This article has been cited by other articles:

				J. M. Banales, T. V. Masyuk, P. S. Bogert, B. Q. Huang, S. A. Gradilone, S.-O. Lee, A. J. Stroope, A. I. Masyuk, J. F. Medina, and N. F. LaRusso Hepatic Cystogenesis Is Associated with Abnormal Expression and Location of Ion Transporters and Water Channels in an Animal Model of Autosomal Recessive Polycystic Kidney Disease Am. J. Pathol., December 1, 2008; 173(6): 1637 - 1646. [Abstract] [Full Text] [PDF]