Abstract
1. Voltage-independent whole-cell Cl- currents were recorded from both single, isolated parietal cells and parietal cells within gastric glands obtained from the fundus of guinea-pig stomach. 2. The Cl- currents were rapidly suppressed by a Cl- channel blocker, NPPB (5-nitro-2-(3-phenylpropylamino)-benzoate), added to the (basolateral) bathing solution in a concentration-dependent manner with a half-maximal inhibition concentration of 12 microM. 3. The selectivity sequence among anions was I- > Br- > Cl- > F-, corresponding to Eisenman's sequence I. 4. The Cl- currents were independent of cytosolic Ca2+, cyclic AMP, cyclic GMP, GTP-gamma-S and cell volume, and were not affected by application of acid secretagogues, omeprazol, arachidonic acid or prostaglandin E2. 5. Reduction of pH in the (basolateral) bathing solution immediately inhibited the Cl- current with a pK (-log of KD) of 6.3, whereas changes in intracellular pH had no effect. 6. The single-channel conductance was estimated to be 0.46-0.6 pS by variance noise analysis during inhibition of whole-cell Cl- currents by NPPB or acidic pH. 7. It is concluded that pH-sensitive 'mini' Cl- channels, with a sub-picosiemens unitary conductance, exist in the basolateral membrane of guinea-pig parietal cells.
Full text
PDF







Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cahalan M. D., Lewis R. S. Role of potassium and chloride channels in volume regulation by T lymphocytes. Soc Gen Physiol Ser. 1988;43:281–301. [PubMed] [Google Scholar]
- Cuppoletti J., Baker A. M., Malinowska D. H. Cl- channels of the gastric parietal cell that are active at low pH. Am J Physiol. 1993 Jun;264(6 Pt 1):C1609–C1618. doi: 10.1152/ajpcell.1993.264.6.C1609. [DOI] [PubMed] [Google Scholar]
- Demarest J. R., Loo D. D. Electrophysiology of the parietal cell. Annu Rev Physiol. 1990;52:307–319. doi: 10.1146/annurev.ph.52.030190.001515. [DOI] [PubMed] [Google Scholar]
- Doroshenko P., Neher E. Volume-sensitive chloride conductance in bovine chromaffin cell membrane. J Physiol. 1992 Apr;449:197–218. doi: 10.1113/jphysiol.1992.sp019082. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Doroshenko P., Penner R., Neher E. Novel chloride conductance in the membrane of bovine chromaffin cells activated by intracellular GTP gamma S. J Physiol. 1991 May;436:711–724. doi: 10.1113/jphysiol.1991.sp018575. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Drouin H., Neumcke B. Specific and unspecific charges at the sodium channels of the nerve membrane. Pflugers Arch. 1974;351(3):207–229. doi: 10.1007/BF00586919. [DOI] [PubMed] [Google Scholar]
- Evans M. G., Marty A. Calcium-dependent chloride currents in isolated cells from rat lacrimal glands. J Physiol. 1986 Sep;378:437–460. doi: 10.1113/jphysiol.1986.sp016229. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Forte J. G., Hanzel D. K., Urushidani T., Wolosin J. M. Pumps and pathways for gastric HCl secretion. Ann N Y Acad Sci. 1989;574:145–158. doi: 10.1111/j.1749-6632.1989.tb25153.x. [DOI] [PubMed] [Google Scholar]
- Gray M. A., Greenwell J. R., Argent B. E. Secretin-regulated chloride channel on the apical plasma membrane of pancreatic duct cells. J Membr Biol. 1988 Oct;105(2):131–142. doi: 10.1007/BF02009166. [DOI] [PubMed] [Google Scholar]
- Gray M. A., Harris A., Coleman L., Greenwell J. R., Argent B. E. Two types of chloride channel on duct cells cultured from human fetal pancreas. Am J Physiol. 1989 Aug;257(2 Pt 1):C240–C251. doi: 10.1152/ajpcell.1989.257.2.C240. [DOI] [PubMed] [Google Scholar]
- HARRIS J. B., EDELMAN I. S. CHEMICAL CONCENTRATION GRADIENTS AND ELECTRICAL PROPERTIES OF GASTRIC MUCOSA. Am J Physiol. 1964 Apr;206:769–782. doi: 10.1152/ajplegacy.1964.206.4.769. [DOI] [PubMed] [Google Scholar]
- Hille B. Charges and potentials at the nerve surface. Divalent ions and pH. J Gen Physiol. 1968 Feb;51(2):221–236. doi: 10.1085/jgp.51.2.221. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ho M. W., Duszyk M., French A. S. Evidence that channels below 1 pS cause the volume-sensitive chloride conductance in T84 cells. Biochim Biophys Acta. 1994 Apr 20;1191(1):151–156. doi: 10.1016/0005-2736(94)90243-7. [DOI] [PubMed] [Google Scholar]
- Hoppe D., Lux H. D., Schachner M., Kettenmann H. Activation of K+ currents in cultured Schwann cells is controlled by extracellular pH. Pflugers Arch. 1989 Oct;415(1):22–28. doi: 10.1007/BF00373137. [DOI] [PubMed] [Google Scholar]
- Klöckner U. Intracellular calcium ions activate a low-conductance chloride channel in smooth-muscle cells isolated from human mesenteric artery. Pflugers Arch. 1993 Aug;424(3-4):231–237. doi: 10.1007/BF00384347. [DOI] [PubMed] [Google Scholar]
- Kotera T., Hashimoto A., Ueda S., Okada Y. Whole-cell K+ current activation in response to voltages and carbachol in gastric parietal cells isolated from guinea pig. J Membr Biol. 1991 Oct;124(1):43–52. doi: 10.1007/BF01871363. [DOI] [PubMed] [Google Scholar]
- Lewis R. S., Ross P. E., Cahalan M. D. Chloride channels activated by osmotic stress in T lymphocytes. J Gen Physiol. 1993 Jun;101(6):801–826. doi: 10.1085/jgp.101.6.801. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marty A., Tan Y. P., Trautmann A. Three types of calcium-dependent channel in rat lacrimal glands. J Physiol. 1984 Dec;357:293–325. doi: 10.1113/jphysiol.1984.sp015501. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marunaka Y., Eaton D. C. Chloride channels in the apical membrane of a distal nephron A6 cell line. Am J Physiol. 1990 Feb;258(2 Pt 1):C352–C368. doi: 10.1152/ajpcell.1990.258.2.C352. [DOI] [PubMed] [Google Scholar]
- Matthews G., Neher E., Penner R. Chloride conductance activated by external agonists and internal messengers in rat peritoneal mast cells. J Physiol. 1989 Nov;418:131–144. doi: 10.1113/jphysiol.1989.sp017831. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Muallem S., Burnham C., Blissard D., Berglindh T., Sachs G. Electrolyte transport across the basolateral membrane of the parietal cells. J Biol Chem. 1985 Jun 10;260(11):6641–6653. [PubMed] [Google Scholar]
- Nilius B., Oike M., Zahradnik I., Droogmans G. Activation of a Cl- current by hypotonic volume increase in human endothelial cells. J Gen Physiol. 1994 May;103(5):787–805. doi: 10.1085/jgp.103.5.787. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pollard C. E., Harris A., Coleman L., Argent B. E. Chloride channels on epithelial cells cultured from human fetal epididymis. J Membr Biol. 1991 Dec;124(3):275–284. doi: 10.1007/BF01994360. [DOI] [PubMed] [Google Scholar]
- Sakai H., Okada Y., Morii M., Takeguchi N. Arachidonic acid and prostaglandin E2 activate small-conductance Cl- channels in the basolateral membrane of rabbit parietal cells. J Physiol. 1992 Mar;448:293–306. doi: 10.1113/jphysiol.1992.sp019042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sakai H., Takeguchi N. Small-conductance Cl- channels in rabbit parietal cells activated by prostaglandin E2 and inhibited by GTP gamma S. J Physiol. 1993 Feb;461:201–212. doi: 10.1113/jphysiol.1993.sp019509. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schettino T., Trischitta F. Transport properties of the basolateral membrane of the oxyntic cells in frog fundic gastric mucosa. Pflugers Arch. 1989 Aug;414(4):469–476. doi: 10.1007/BF00585059. [DOI] [PubMed] [Google Scholar]
- Stoddard J. S., Steinbach J. H., Simchowitz L. Whole cell Cl- currents in human neutrophils induced by cell swelling. Am J Physiol. 1993 Jul;265(1 Pt 1):C156–C165. doi: 10.1152/ajpcell.1993.265.1.C156. [DOI] [PubMed] [Google Scholar]
- Taleb O., Feltz P., Bossu J. L., Feltz A. Small-conductance chloride channels activated by calcium on cultured endocrine cells from mammalian pars intermedia. Pflugers Arch. 1988 Oct;412(6):641–646. doi: 10.1007/BF00583766. [DOI] [PubMed] [Google Scholar]
- Waisbren S. J., Geibel J., Boron W. F., Modlin I. M. Luminal perfusion of isolated gastric glands. Am J Physiol. 1994 Apr;266(4 Pt 1):C1013–C1027. doi: 10.1152/ajpcell.1994.266.4.C1013. [DOI] [PubMed] [Google Scholar]
- Woodhull A. M. Ionic blockage of sodium channels in nerve. J Gen Physiol. 1973 Jun;61(6):687–708. doi: 10.1085/jgp.61.6.687. [DOI] [PMC free article] [PubMed] [Google Scholar]
