Aquaporin-5 dependent fluid secretion in airway submucosal glands.

被引:173
作者
Song, YL
Verkman, AS
机构
[1] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Cardiovasc Res Inst, Dept Physiol, San Francisco, CA 94143 USA
关键词
D O I
10.1074/jbc.M107257200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fluid and macromolecule secretion by submucosal glands in mammalian airways is believed to play an important role in airway defense and surface liquid homeostasis and in the pathogenesis of cystic fibrosis. Immunocytochemistry revealed strong expression of aquaporin water channel AQP5 at the luminal membrane of serous epithelial cells in submucosal glands throughout the mouse nasopharynx and upper airways and AQP4 at the contralateral basolateral membrane in some glands. Novel methods were applied to measure secretion rates and composition of gland fluid in wild type mice and knockout mice lacking AQP4 or AQP5. In mice breathing through a tracheotomy, total gland fluid output was measured from the dilution of a volume marker present in the fluid-filled nasopharynx and upper trachea. Pilocarpine-stimulated fluid secretion was 4.3 +/- 0.4 mul/min in wild type mice, 4.9 +/- 0.9 mul/min in AQP4 null mice, and 1.9.+/- 0.3 mul/min in AQP5 null mice (p < 0.001). Similar results were obtained when secreted fluid was collected in the oil-filled nasopharyngeal cavity. Real-time video imaging of fluid droplets secreted from individual submucosal glands near the larynx in living mice showed a 57 +/- 4% reduced fluid secretion rate in AQP5 null mice. Analysis of secreted fluid showed a 2.3 +/- 0.2-fold increase in total protein in AQP5 null mice and a smaller increase in [Cl-], suggesting intact protein and salt secretion across a relatively water impermeable epithelial barrier. Submucosal gland morphology and density did not differ significantly in wild type versus AQP5 null mice. These results indicate that AQP5 facilitates fluid secretion in submucosal glands and that the luminal membrane of gland epithelial cells is the rate-limiting barrier to water movement. Modulation of gland AQP5 expression or function might provide a novel approach to treat hyperviscous gland secretions in cystic fibrosis and excessive fluid secretions in infectious or allergic bronchitis/rhinitis.
引用
收藏
页码:41288 / 41292
页数:5
相关论文
共 33 条
[1]   Lung fluid transport in aquaporin-1 and aquaporin-4 knockout mice [J].
Bai, CX ;
Fukuda, N ;
Song, YL ;
Ma, TH ;
Matthay, MA ;
Verkman, AS .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (04) :555-561
[2]  
BASBAUM CB, 1990, ANNU REV PHYSIOL, V52, P97
[3]   Effect of uridine 5'-triphosphate plus amiloride on mucociliary clearance in adult cystic fibrosis [J].
Bennett, WD ;
Olivier, KN ;
Zeman, KL ;
Hohneker, KW ;
Boucher, RC ;
Knowles, MR .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (06) :1796-1801
[4]   Molecular insights into the physiology of the 'thin film' of airway surface liquid [J].
Boucher, RC .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 516 (03) :631-638
[5]   DEFECTIVE INTRACELLULAR-TRANSPORT AND PROCESSING OF CFTR IS THE MOLECULAR-BASIS OF MOST CYSTIC-FIBROSIS [J].
CHENG, SH ;
GREGORY, RJ ;
MARSHALL, J ;
PAUL, S ;
SOUZA, DW ;
WHITE, GA ;
ORIORDAN, CR ;
SMITH, AE .
CELL, 1990, 63 (04) :827-834
[6]   A comparative study of mammalian tracheal mucous glands [J].
Choi, HK ;
Finkbeiner, WE ;
Widdicombe, JH .
JOURNAL OF ANATOMY, 2000, 197 :361-372
[7]  
FUNAKI H, 1997, AM J PHYSIOL, V272, pL203
[8]  
GIROD S, 1992, EUR RESPIR J, V5, P477
[9]   Hypertonic induction of aquaporin-5 expression through an ERK-dependent pathway [J].
Hoffert, JD ;
Leitch, V ;
Agre, P ;
King, LS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) :9070-9077
[10]   In situ visualization of bronchial submucosal glands and their secretory response to acetylcholine [J].
Inglis, SK ;
Corboz, MR ;
Taylor, AE ;
Ballard, ST .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1997, 272 (02) :L203-L210