Protease-activated receptor-2-mediated inhibition of ion transport in human bronchial epithelial cells

被引:43
作者
Danahay, H
Withey, L
Poll, CT
Van De Graaf, SFJ
Bridges, RJ
机构
[1] Novartis Horsham Res Ctr, Horsham RH12 5AB, W Sussex, England
[2] Univ Pittsburgh, Dept Cell Biol & Physiol, Pittsburgh, PA 15261 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2001年 / 280卷 / 06期
关键词
trypsin; epithelial sodium channel; human airway;
D O I
10.1152/ajpcell.2001.280.6.C1455
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A cytoprotective role for protease-activated receptor-2 (PAR2) has been suggested in a number of systems including the airway, and to this end, we have studied the role that PARs play in the regulation of airway ion transport, using cultures of normal human bronchial epithelial cells. PAR2 activators, added to the basolateral membrane, caused a transient, Ca2+-dependent increase in short-circuit current (I-sc), followed by a sustained inhibition of amiloride- sensitive I-sc. These phases corresponded with a transient increase in intracellular Ca2+ concentration and then a transient increase, followed by decrease, in basolateral K+ permeability. After PAR2 activation and the addition of amiloride, the forskolin-stimulated increase in Isc was also attenuated. By contrast, PAR2 activators added to the apical surface of the epithelia or PAR1 activators added to both the apical and basolateral surfaces were without effect. PAR2 may, therefore, play a role in the airway, regulating Na+ absorption and anion secretion, processes that are central to the control of airway surface liquid volume and composition.
引用
收藏
页码:C1455 / C1464
页数:10
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