Distinct Ca2+- and cAMP-dependent anion conductances in the apical membrane of polarized T84 cells

被引:50
作者
Merlin, D
Jiang, LW
Strohmeier, GR
Nusrat, A
Alper, SL
Lencer, WI
Madara, JL
机构
[1] Brigham & Womens Hosp, Dept Pathol, Div Gastrointestinal Pathol, Boston, MA 02115 USA
[2] Beth Israel Deaconess Med Ctr, Mol Med Unit, Boston, MA 02115 USA
[3] Beth Israel Deaconess Med Ctr, Renal Unit, Boston, MA 02115 USA
[4] Childrens Hosp, Med Ctr, Combined Program Pediat Gastroenterol & Nutr, Dept Med, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Boston, MA 02115 USA
[6] Harvard Digest Dis Ctr, Boston, MA 02115 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1998年 / 275卷 / 02期
关键词
intestinal epithelium; thapsigargin; forskolin; chloride channels; amphotericin B; human intestinal cell line T84;
D O I
10.1152/ajpcell.1998.275.2.C484
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Monolayers of the human colonic epithelial cell Line T84 exhibit electrogenic Cl- secretion in response to the Ca2+ agonist thapsigargin and to the cAMP agonist forskolin. To evaluate directly the regulation of apical Cl- conductance by these two agonists, we have utilized amphotericin B to permeabilize selectively the basolateral membranes of T84 cell monolayers. We find that apical anion conductance is stimulated by both forskolin and thapsigargin but that these conductances are differentially sensitive to the anion channel blocker DIDS. DIDS inhibits thapsigargin-stimulated responses completely but forskolin responses only partially Furthermore, the apical membrane anion conductances elicited by these two agonists differ in anion selectivity (for thapsigargin, I- > Cl-; for forskolin, Cl- > I-). However, the DIDS-sensitive component of the forskolin-induced conductance response exhibits anion selectivity similar to that induced by thapsigargin (I- > Cl-). Thus forskolin-induced apical anion conductance comprises at least two components, one of which has features in common with that elicited by thapsigargin.
引用
收藏
页码:C484 / C495
页数:12
相关论文
共 43 条
[1]  
ANDERSON P, 1991, P NATL ACAD SCI USA, V88, P603
[2]   BIPHASIC INCREASE OF APICAL CL- CONDUCTANCE BY MUSCARINIC STIMULATION OF HT-29CL.19A HUMAN COLON-CARCINOMA CELL-LINE - EVIDENCE FOR ACTIVATION OF DIFFERENT CL- CONDUCTANCES BY CARBACHOL AND FORSKOLIN [J].
BAJNATH, RB ;
DEKKER, K ;
VAANDRAGER, AB ;
DEJONGE, HR ;
GROOT, JA .
JOURNAL OF MEMBRANE BIOLOGY, 1992, 127 (02) :81-94
[3]   Inhibition of Ca2+-dependent Cl- secretion in T84 cells:: membrane target(s) of inhibition is agonist specific [J].
Barrett, KE ;
Smitham, J ;
Traynor-Kaplan, A ;
Uribe, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 274 (04) :C958-C965
[4]  
BARRETT KE, 1993, AM J PHYSIOL, V265, pC859
[5]   Integrated regulation of intestinal epithelial transport: Intercellular and intracellular pathways [J].
Barrett, KE .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 272 (04) :C1069-C1076
[6]   T84 CELLS - ANION SELECTIVITY DEMONSTRATES EXPRESSION OF CL- CONDUCTANCE AFFECTED IN CYSTIC-FIBROSIS [J].
BELL, CL ;
QUINTON, PM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (03) :C555-C562
[7]   CA IONOPHORE-STIMULATED ION SECRETION IN RABBIT ILEAL MUCOSA - RELATION TO ACTIONS OF CYCLIC 3',5'-AMP AND CARBAMYLCHOLINE [J].
BOLTON, JE ;
FIELD, M .
JOURNAL OF MEMBRANE BIOLOGY, 1977, 35 (02) :159-173
[8]  
BRAYDEN DJ, 1993, AM J PHYSIOL, V264, pC325
[9]   SEPARATE CL- CONDUCTANCES ACTIVATED BY CAMP AND CA-2+ IN CL--SECRETING EPITHELIAL-CELLS [J].
CLIFF, WH ;
FRIZZELL, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :4956-4960
[10]   LOCALIZATION OF CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR IN CHLORIDE SECRETORY EPITHELIA [J].
DENNING, GM ;
OSTEDGAARD, LS ;
CHENG, SH ;
SMITH, AE ;
WELSH, MJ .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (01) :339-349