Epinephrine stimulation of anion secretion in the Calu-3 serous cell model

被引:14
作者
Banga, Amiraj [1 ]
Flaig, Stephanie [1 ]
Lewis, Shanta [1 ]
Winfree, Seth [2 ]
Blazer-Yost, Bonnie L. [1 ,3 ]
机构
[1] Indiana Univ Purdue Univ, Dept Biol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Div Nephrol, Indianapolis, IN USA
[3] Indiana Univ, Sch Med, Dept Cellular & Integrat Physiol, Indianapolis, IN USA
关键词
cystic fibrosis transmembrane conductance regulator; transmembrane protein 16A; transepithelial ion transport; airway epithelia; mucociliary clearance; AIRWAY EPITHELIAL-CELLS; CHLORIDE SECRETION; CYSTIC-FIBROSIS; FLUID ABSORPTION; CL-SECRETION; CFTR; TMEM16A; LUNG; EXPRESSION; CHANNELS;
D O I
10.1152/ajplung.00190.2013
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Calu-3 is a well-differentiated human bronchial cell line with the characteristics of the serous cells of airway submucosal glands. The submucosal glands play a major role in mucociliary clearance because they secrete electrolytes that facilitate airway hydration. Given the significance of both long-and short-term beta-adrenergic receptor agonists in the treatment of respiratory diseases, it is important to determine the role of these receptors and their ligands in normal physiological function. The present studies were designed to characterize the effect of epinephrine, the naturally occurring beta-adrenergic receptor agonist, on electrolyte transport of the airway serous cells. Interestingly, epinephrine stimulated two anion secretory channels, the cystic fibrosis transmembrane conductance regulator and a Ca2+ - activated Cl- channel, with the characteristics of transmembrane protein 16A, thereby potentially altering mucociliary clearance via multiple channels. Consistent with the dual channel activation, epinephrine treatment resulted in increases in both intracellular cAMP and Ca2+. Furthermore, the present results extend previous reports indicating that the two anion channels are functionally linked.
引用
收藏
页码:L937 / L946
页数:10
相关论文
共 41 条
[1]   Expression of functional β2-adrenergic receptors in the lung epithelial cell lines 16HBE14o-, Calu-3 and A549 [J].
Abraham, G ;
Kneuer, C ;
Ehrhardt, C ;
Honscha, W ;
Ungemach, FR .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1691 (2-3) :169-179
[2]   Functional Effects of Nanoparticle Exposure on Calu-3 Airway Epithelial Cells [J].
Banga, Amiraj ;
Witzmann, Frank A. ;
Petrache, Horia I. ;
Blazer-Yost, Bonnie L. .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2012, 29 (1-2) :197-212
[3]   BETA-ADRENERGIC AGONISTS INCREASE LUNG LIQUID CLEARANCE IN ANESTHETIZED SHEEP [J].
BERTHIAUME, Y ;
STAUB, NC ;
MATTHAY, MA .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (02) :335-343
[4]   The secret life of CFTR as a calcium-activated chloride channel [J].
Billet, Arnaud ;
Hanrahan, John W. .
JOURNAL OF PHYSIOLOGY-LONDON, 2013, 591 (21) :5273-5278
[5]   TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity [J].
Caputo, Antonella ;
Caci, Emanuela ;
Ferrera, Loretta ;
Pedemonte, Nicoletta ;
Barsanti, Cristina ;
Sondo, Elvira ;
Pfeffer, Ulrich ;
Ravazzolo, Roberto ;
Zegarra-Moran, Olga ;
Galietta, Luis J. V. .
SCIENCE, 2008, 322 (5901) :590-594
[6]   TANNIN INHIBITS CAMP PATHWAYS IN BOVINE AIRWAY EPITHELIUM [J].
CLOUTIER, MM ;
GUERNSEY, L ;
SHAAFI, RI .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (01) :106-112
[7]   Bicarbonate-dependent chloride secretion in Calu-3 epithelia in response to 7,8-benzoquinoline [J].
Cuthbert, AW ;
Supuran, CT ;
MacVinish, LJ .
JOURNAL OF PHYSIOLOGY-LONDON, 2003, 551 (01) :79-92
[8]   Bicarbonate and chloride secretion in Calu-3 human airway epithelial cells [J].
Devor, DC ;
Singh, AK ;
Lambert, LC ;
DeLuca, A ;
Frizzell, RA ;
Bridges, RJ .
JOURNAL OF GENERAL PHYSIOLOGY, 1999, 113 (05) :743-760
[9]  
Finkbeiner WE, 1992, TREATISE PULMONARY T, V1, P633
[10]   Alveolar epithelial fluid clearance is mediated by endogenous catecholamines at birth in guinea pigs [J].
Finley, N ;
Norlin, A ;
Baines, DL ;
Folkesson, HG .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (05) :972-981