Heterotrimeric G-proteins activate Cl- channels through stimulation of a cyclooxygenase-dependent pathway in a model liver cell line

Gordan Kilic, J. Gregory Fitz

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Abstract

Circulating hormones produce rapid changes in the Cl- permeability of liver cells through activation of plasma membrane receptors coupled to heterotrimeric G-proteins. The resulting effects on intracellular pH, membrane potential, and Cl- content are important contributors to the overall metabolic response. Consequently, the purpose of these studies was to evaluate the mechanisms responsible for G-protein-mediated changes in membrane Cl- permeability using HTC hepatoma cells as a model. Using patch clamp techniques, intracellular dialysis with 0.3 mM guanosine 5′-O-(3-thiotriphosphate) (GTPγS) increased membrane conductance from 10 to 260 picosiemens/picofarads due to activation of Ca2+-dependent Cl- currents that were outwardly rectifying and exhibited slow activation at depolarizing potentials. These effects were mimicked by intracellular AlF4 - (0.03 mM) and inhibited by pertussis toxin (PTX), consistent with current activation through Gαi. Studies using defined agonists and inhibitors indicate that Cl- channel activation by GTPγS occurs through an indomethacin-sensitive pathway involving sequential activation of phospholipase C, mobilization of Ca2+ from inositol 1,4,5-trisphosphate-sensitive stores, and stimulation of phospholipase A2 and cyclooxygenase (COX). Accordingly, the conductance responses to GTPγS or to intracellular Ca2+ were inhibited by COX inhibitors. These results indicate that PTX-sensitive G-proteins regulate the Cl- permeability of HTC cells through Ca2+-dependent stimulation of COX activity. Thus, receptor-mediated activation of Gαi may be essential for hormonal regulation of liver transport and metabolism through COX-dependent opening of a distinct population of plasma membrane Cl- channels.

Original languageEnglish (US)
Pages (from-to)11721-11727
Number of pages7
JournalJournal of Biological Chemistry
Volume277
Issue number14
DOIs
Publication statusPublished - Apr 5 2002

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ASJC Scopus subject areas

  • Biochemistry

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