Am. J. Respir. Cell Mol. Biol.,
Volume 24, Number 2, February, 2001 195-202
New Models of the Tracheal Airway Define the Glandular Contribution to
Airway Surface Fluid and Electrolyte Composition
Xiaorong
Wang,
Yulong
Zhang,
Anson
Amberson,
and
John F.
Engelhardt
Departments of Anatomy and Cell Biology, and Internal Medicine, College of Medicine, University of Iowa, Iowa City, Iowa
Antibacterial defenses in the airway are dependent on multifactorial influences that determine the composition of both
fluid and/or electrolytes at the surface of the airway and the
secretory products that aid in bacterial killing and clearance.
In cystic fibrosis (CF), these mechanisms of airway protection
may be defective, leading to increased colonization with
Pseudomonas aeruginosa. Submucosal glands, a predominant
site of cystic fibrosis transmembrane conductance regulator
(CFTR) protein expression in the airway, have been hypothesized to play an important role in protection of the airway.
Furthermore, recent studies have suggested that the salt concentration at the airway surface may be a key factor in regulating the activity of antibacterial substances in the airway. To
explore these issues, we have used a new model of the ferret
tracheal airway to evaluate the contribution of submucosal glands in regulating airway surface fluid and electrolyte composition. Using tracheal xenograft models with and without
submucosal glands, we have characterized several aspects of
airway physiology that may be important in defining antibacterial properties. These endpoints included the contribution
of submucosal glands in defining bioelectric properties of the
surface airway epithelium, airway surface fluid (ASF) chloride
composition, ASF volumes, and secretion of the antibacterial
factor lysozyme. Findings from these studies demonstrate a
significantly elevated secreted fluid volume (Vs) and chloride concentration ([Cl]s) in ASF from airways with submucosal
glands (Vs = 47 ± 4 µl; [Cl]s = 128 ± 5 mM), as compared
with xenograft airways without glands (Vs = 36 ± 2 µl; [Cl]s = 103 ± 6 mM). Furthermore, a temperature labile factor secreted by submucosal glands appears to alter the baseline
activation of 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid
and/or diphenylamine-2-carboxylic acid-sensitive chloride channels in the surface airway epithelium. Lastly, the lysozyme content of tracheal airways with submucosal glands was 8.5-fold higher than were airways without glands. These studies demonstrate that submucosal glands affect both the ionic composition and bioelectric properties of the airway and suggest
that models evaluating antibacterial properties of the airway
in CF should take into account the contribution of glands in
airway physiology.
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Copyright © 2001 American Thoracic Society.
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