Membrane capacitance and conductance changes parallel mucin secretion in the human airway epithelium

被引:26
作者
Danahay, H
Atherton, HC
Jackson, AD
Kreindler, JL [1 ]
Poll, CT
Bridges, RJ
机构
[1] Univ Pittsburgh, Dept Pediat, Pittsburgh, PA 15213 USA
[2] Novartis Inst Biomed Res, Horsham, W Sussex, England
[3] Rosalind Franklin Univ Med & Sci, Dept Physiol & Biophys, N Chicago, IL USA
关键词
degranulation; exocytosis; goblet cell; impedance analysis; mucus;
D O I
10.1152/ajplung.00351.2005
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Measurement of the magnitude and kinetics of exocytosis from intact epithelia has historically been difficult. Using well-differentiated cultures of human bronchial epithelial cells, we describe the use of transepithelial impedance analysis to enable the real-time quantification of mucin secretagogue-induced changes in membrane capacitance (surface area) and conductance. ATP gamma S, UTP, ionomycin, and PMA induced robust increases in total cellular capacitance that were demonstrated to be dominated by a specific increase in apical membrane surface area. The UTP-induced increase in capacitance occurred in parallel with goblet cell emptying and the secretion of mucin and was associated with decreases in apical and basolateral membrane resistances. The magnitude and kinetics of the capacitance increases were dependent on the agonist and the sidedness of the stimulation. The peak increase in capacitance induced by UTP was similar to 30 mucin granule fusions per goblet cell. Secretagogue-induced decreases in apical membrane resistance were independent of exocytosis, although each of the secretagogues induced profound reductions in basolateral membrane resistance. Transepithelial impedance analysis offers the potential to study morphological and conductance changes in cultured human bronchial epithelial cells.
引用
收藏
页码:L558 / L569
页数:12
相关论文
共 36 条
[1]   Protein kinase C and Ca2+ activation of mucin secretion in airway goblet cells [J].
Abdullah, LH ;
Conway, JD ;
Cohn, JA ;
Davis, CW .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1997, 273 (01) :L201-L210
[2]   Purinergic and cholinergic agonists induce exocytosis from the same granule pool in HT29-Cl.16E monolayers [J].
Bertrand, CA ;
Laboisse, CL ;
Hopfer, U .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (04) :C907-C914
[3]   System for dynamic measurements of membrane capacitance in intact epithelial monolayers [J].
Bertrand, CA ;
Durand, DM ;
Saidel, GM ;
Laboisse, C ;
Hopfer, U .
BIOPHYSICAL JOURNAL, 1998, 75 (06) :2743-2756
[4]   Niflumic acid inhibits ATP-stimulated exocytosis in a mucin-secreting epithelial cell line [J].
Bertrand, CA ;
Danahay, H ;
Poll, CT ;
Laboisse, C ;
Hopfer, U ;
Bridges, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 286 (02) :C247-C255
[5]   The role of regulated CFTR trafficking in epithelial secretion [J].
Bertrand, CA ;
Frizzell, RA .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 285 (01) :C1-C18
[6]   FORSKOLIN INDUCED CHLORIDE SECRETION ACROSS THE ISOLATED MUCOSA OF RAT COLON DESCENDENS [J].
BRIDGES, RJ ;
RUMMEL, W ;
SIMON, B .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1983, 323 (04) :355-360
[7]   The relationship between cAMP, Ca2+, and transport of CFTR to the plasma membrane [J].
Chen, P ;
Hwang, TC ;
Gillis, KD .
JOURNAL OF GENERAL PHYSIOLOGY, 2001, 118 (02) :135-144
[8]   Interleukin-13 induces a hypersecretory ion transport phenotype in human bronchial epithelial cells [J].
Danahay, H ;
Atherton, H ;
Jones, G ;
Bridges, RJ ;
Poll, CT .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2002, 282 (02) :L226-L236
[9]   GOBLET CELL DEGRANULATION IN ISOLATED CANINE TRACHEAL EPITHELIUM - RESPONSE TO EXOGENOUS ATP, ADP, AND ADENOSINE [J].
DAVIS, CW ;
DOWELL, ML ;
LETHEM, M ;
VANSCOTT, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (05) :C1313-C1323
[10]   Pharmacological modulation of ion transport across wild-type and ΔF508 CFTR-expressing human bronchial epithelia [J].
Devor, DC ;
Bridges, RJ ;
Pilewski, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2000, 279 (02) :C461-C479