|
|
||||||||
AJP - Gastrointestinal and Liver Physiology, Vol 264, Issue 2 325-G333, Copyright © 1993 by American Physiological Society
ARTICLES |
D. J. Brayden, M. E. Krouse, T. Law and J. J. Wine
Cystic Fibrosis Research Laboratory, Stanford University, California 94305-2130.
Basolateral but not apical application of 10-200 microM 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid (DIDS) or 4-acetamido-4'-isothiocyanostilbene-2,2'-disulfonic acid (SITS) to T84 monolayers produced a transient increase in short-circuit current (Isc), followed by a sustained inhibition. 4,4'-Dinitrostilbene-2,2'-disulfonic acid (DNDS) had no effect. The increase in Isc produced by DIDS represents Cl- secretion and appears to result from Ca2+ elevation, because in all respects except time course the response to DIDS mimicked the response to the Ca(2+)-elevating agent thapsigargin. Fura-2 measurements established that thapsigargin elevates Ca2+ in T84 cells, but Ca2+ responses to DIDS could not be established directly because DIDS absorbs strongly at the critical wavelengths. Responses to DIDS and thapsigargin were 1) blocked by bumetanide; 2) not blocked by basolateral Ba2+; 3) completely nonadditive; 4) strongly synergistic with basal levels of Isc or with Isc increases produced by elevating adenosine 3',5'-cyclic monophosphate (cAMP; with forskolin) or guanosine 3',5'-cyclic monophosphate (with heat-stable enterotoxin); and 5) reversibly abolished by removal of basolateral Ca2+. Interactions between Ca2+ and cAMP-elevating agents strongly support a model of Cl- secretion in which apical Cl- conductance is activated by cyclic nucleotides but not by Ca2+ while basolateral K+ channels are activated by Ca2+. In contrast with this mechanism, whole cell patch-clamp recordings of nonconfluent T84 cells indicated that DIDS and other Ca(2+)-elevating agents stimulated an increase in Cl- conductance. Thus increases in cytosolic free Ca2+ in nonconfluent T84 cells activate conductances that differ from those in confluent monolayers.
This article has been cited by other articles:
![]() |
S. K. Fellner and W. J. Arendshorst Angiotensin II-stimulated Ca2+ entry mechanisms in afferent arterioles: role of transient receptor potential canonical channels and reverse Na+/Ca2+ exchange Am J Physiol Renal Physiol, January 1, 2008; 294(1): F212 - F219. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. N. Chernova, D. H. Vandorpe, J. S. Clark, J. I. Williams, M. A. Zasloff, L. Jiang, and S. L. Alper Apparent receptor-mediated activation of Ca2+-dependent conductive Cl- transport by shark-derived polyaminosterols Am J Physiol Regulatory Integrative Comp Physiol, December 1, 2005; 289(6): R1644 - R1658. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E. Krouse, J. F. Talbott, M. M. Lee, N. S. Joo, and J. J. Wine Acid and base secretion in the Calu-3 model of human serous cells Am J Physiol Lung Cell Mol Physiol, December 1, 2004; 287(6): L1274 - L1283. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. J. Szkotak, S. F. P. Man, and M. Duszyk The Role of the Basolateral Outwardly Rectifying Chloride Channel in Human Airway Epithelial Anion Secretion Am. J. Respir. Cell Mol. Biol., December 1, 2003; 29(6): 710 - 720. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. L. Carrithers Diarrhea or colorectal cancer: Can bacterial toxins serve as a treatment for colon cancer? PNAS, March 18, 2003; 100(6): 3018 - 3020. [Full Text] [PDF] |
||||
![]() |
B. D. SCHULTZ, A. K. SINGH, D. C. DEVOR, and R. J. BRIDGES Pharmacology of CFTR Chloride Channel Activity Physiol Rev, January 1, 1999; 79(1): 109 - 144. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Merlin, L. Jiang, G. R. Strohmeier, A. Nusrat, S. L. Alper, W. I. Lencer, and J. L. Madara Distinct Ca2+- and cAMP-dependent anion conductances in the apical membrane of polarized T84 cells Am J Physiol Cell Physiol, August 1, 1998; 275(2): C484 - C495. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Moon, M. Singh, M. E. Krouse, and J. J. Wine Calcium-stimulated Cl- secretion in Calu-3 human airway cells requires CFTR Am J Physiol Lung Cell Mol Physiol, December 1, 1997; 273(6): L1208 - L1219. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |