Characterization of high-conductance anion channels in rat bile duct epithelial cells
- PMID: 1373566
- DOI: 10.1152/ajpgi.1992.262.4.G703
Characterization of high-conductance anion channels in rat bile duct epithelial cells
Abstract
We have utilized patch clamp recording techniques to identify a high-conductance anion channel in the plasma membrane of rat bile duct epithelial cells. Cells were isolated from the intrahepatic bile duct 2-6 wk after bile duct ligation. Channels were present in 27% (28/102) of excised patches, and, with 150 mM Cl- in bath and pipette solutions, the slope conductance of the fully open level was approximately 364 +/- 18 pS (n = 8) with current reversal = 0 +/- 1 mV. Channel characteristics were not affected by substitution of K+ for Na+ in the pipette solution; but substitution of HCO3-, gluconate, or increased NaCl caused a shift in the reversal potential toward the new equilibrium potential for Cl-. The permeability ratios were PHCO3-/PCl- = 0.51 +/- 0.03 (n = 5), Pgluconate/PCl- = 0.12 +/- 0.04 (n = 7), and PNa+/PCl- = 0.11 +/- 0.02 (n = 3). Current transitions to a subconductance level at 72% of the fully open level were present in most studies. Channel open probability was greatest near 0 mV and decreased rapidly outside of -20 to +20 mV because of voltage-dependent channel closure. The time course for current relaxation of summed single channel currents could be described by a single exponential with more rapid channel closure as the magnitude of the voltage step away from 0 mV increased. In the cell-attached configuration, the channel was rarely open (4/35, 11%) but opening could be induced by negative pipette pressure (5/14, 35%). Possible physiological roles for this channel are discussed.
Similar articles
-
GTP-binding proteins regulate high conductance anion channels in rat bile duct epithelial cells.J Membr Biol. 1993 May;133(3):253-61. doi: 10.1007/BF00232024. J Membr Biol. 1993. PMID: 7687295
-
Secretin activates Cl- channels in bile duct epithelial cells through a cAMP-dependent mechanism.Am J Physiol. 1994 Apr;266(4 Pt 1):G731-6. doi: 10.1152/ajpgi.1994.266.4.G731. Am J Physiol. 1994. PMID: 8179008
-
Whole-cell and single channel K+ and Cl- currents in epithelial cells of frog skin.J Gen Physiol. 1991 Jul;98(1):131-61. doi: 10.1085/jgp.98.1.131. J Gen Physiol. 1991. PMID: 1719124 Free PMC article.
-
Endogenous chloride channels of insect sf9 cells. Evidence for coordinated activity of small elementary channel units.J Gen Physiol. 1996 Jun;107(6):695-714. doi: 10.1085/jgp.107.6.695. J Gen Physiol. 1996. PMID: 8783071 Free PMC article. Review.
-
Recent advances in the characterization of epithelial ionic channels.Biochim Biophys Acta. 1987 Apr 27;906(1):1-31. doi: 10.1016/0304-4157(87)90003-7. Biochim Biophys Acta. 1987. PMID: 2436665 Review.
Cited by
-
Regulation of membrane chloride currents in rat bile duct epithelial cells.J Clin Invest. 1993 Jan;91(1):319-28. doi: 10.1172/JCI116188. J Clin Invest. 1993. PMID: 7678606 Free PMC article.
-
ATP release via anion channels.Purinergic Signal. 2005 Dec;1(4):311-28. doi: 10.1007/s11302-005-1557-0. Epub 2005 Dec 3. Purinergic Signal. 2005. PMID: 18404516 Free PMC article.
-
Cholangiocyte anion exchange and biliary bicarbonate excretion.World J Gastroenterol. 2006 Jun 14;12(22):3496-511. doi: 10.3748/wjg.v12.i22.3496. World J Gastroenterol. 2006. PMID: 16773707 Free PMC article. Review.
-
Thiamine in excitable tissues: reflections on a non-cofactor role.Metab Brain Dis. 1994 Sep;9(3):183-209. doi: 10.1007/BF01991194. Metab Brain Dis. 1994. PMID: 7838063 Review. No abstract available.
-
The ATP-Releasing Maxi-Cl Channel: Its Identity, Molecular Partners and Physiological/Pathophysiological Implications.Life (Basel). 2021 May 31;11(6):509. doi: 10.3390/life11060509. Life (Basel). 2021. PMID: 34073084 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources