Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/46234
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Type: Journal article
Title: Store-operated Ca2+ channels and Stromal Interaction Molecule 1 (STIM1) are targets for the actions of bile acids on liver cells
Author: Aromataris, E.
Castro, J.
Rychkov, G.
Barritt, G.
Citation: Biochimica et Biophysica Acta-Molecular Cell Research, 2008; 1783(5):874-885
Publisher: Elsevier Science BV
Issue Date: 2008
ISSN: 0167-4889
0006-3002
Statement of
Responsibility: 
Edoardo C. Aromataris, Joel Castro, Grigori Y. Rychkov and Greg J. Barritt
Abstract: Cholestasis is a significant contributor to liver pathology and can lead to primary sclerosis and liver failure. Cholestatic bile acids induce apoptosis and necrosis in hepatocytes but these effects can be partially alleviated by the pharmacological application of choleretic bile acids. These actions of bile acids on hepatocytes require changes in the release of Ca(2+) from intracellular stores and in Ca(2+) entry. However, the nature of the Ca(2+) entry pathway affected is not known. We show here using whole cell patch clamp experiments with H4-IIE liver cells that taurodeoxycholic acid (TDCA) and other choleretic bile acids reversibly activate an inwardly-rectifying current with characteristics similar to those of store-operated Ca(2+) channels (SOCs), while lithocholic acid (LCA) and other cholestatic bile acids inhibit SOCs. The activation of Ca(2+) entry was observed upon direct addition of the bile acid to the incubation medium, whereas the inhibition of SOCs required a 12 h pre-incubation. In cells loaded with fura-2, choleretic bile acids activated a Gd(3+)-inhibitable Ca(2+) entry, while cholestatic bile acids inhibited the release of Ca(2+) from intracellular stores and Ca(2+) entry induced by 2,5-di-(tert-butyl)-1,4-benzohydro-quinone (DBHQ). TDCA and LCA each caused a reversible redistribution of stromal interaction molecule 1 (STIM1, the endoplasmic reticulum Ca(2+) sensor required for the activation of Ca(2+) release-activated Ca(2+) channels and some other SOCs) to puncta, similar to that induced by thapsigargin. Knockdown of Stim1 using siRNA caused substantial inhibition of Ca(2+)-entry activated by choleretic bile acids. It is concluded that choleretic and cholestatic bile acids activate and inhibit, respectively, the previously well-characterised Ca(2+)-selective hepatocyte SOCs through mechanisms which involve the bile acid-induced redistribution of STIM1.
Keywords: Liver cell; Cholestasis; Ca2+ channel; STIM1; Bile acid; Patch clamp recording
Rights: Copyright © 2008 Elsevier B.V. All rights reserved.
RMID: 0020080711
DOI: 10.1016/j.bbamcr.2008.02.011
Description (link): http://www.elsevier.com/wps/find/journaldescription.cws_home/506069/description#description
Appears in Collections:Molecular and Biomedical Science publications

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