Measurement of Fluid Secretion from Intact Airway Submucosal Glands
myoepithelial cell
Cystic Fibrosis Transmembrane Conductance Regulator/metabolism
572
Cystic Fibrosis
Molecular Imaging/methods*
Mucus*/metabolism
Swine
Cystic Fibrosis Transmembrane Conductance Regulator
Mucous Membrane/metabolism
Respiratory Mucosa
Sputum/metabolism
Exocrine Glands/metabolism*
mucosal innate defense
mucous cell
calcium-activated chloride channel (CaCC)
Mice
Exocrine Glands
Species Specificity
Trachea/cytology
Trachea/metabolism
cAMP
Mucus*/chemistry
Submucosal gland
Animals
Humans
Cystic Fibrosis/metabolism
exocrine secretion
CFTR
Microscopy
Mucous Membrane
Sheep
serous cell
Ferrets
Sputum
ion transporter
Biological Transport
Cystic Fibrosis/physiopathology
Respiratory Mucosa/cytology
Respiratory Mucosa/metabolism*
Body Fluids
Molecular Imaging
Ca2+
Mucus
Mucociliary Clearance
ion channel
Cats
Body Fluids/metabolism
Mucus*/secretion
Mucociliary Clearance*
DOI:
10.1007/978-1-61779-120-8_6
Publication Date:
2011-05-05T22:17:05Z
AUTHORS (12)
ABSTRACT
Human airways are kept sterile by a mucosal innate defense system that includes mucus secretion. Mucus is secreted in healthy upper airways primarily by submucosal glands and consists of defense molecules mixed with mucins, electrolytes, and water and is also a major component of sputum. Mucus traps pathogens and mechanically removes them via mucociliary clearance while inhibiting their growth via molecular (e.g., lysozyme) and cellular (e.g., neutrophils, macrophages) defenses. Fluid secretion rates of single glands in response to various mediators can be measured by trapping the primary gland mucus secretions in an oil layer, where they form spherical bubbles that can be optically measured at any desired interval to provide detailed temporal analysis of secretion rates. The composition and properties of the mucus (e.g., solids, viscosity, pH) can also be determined. These methods have now been applied to mice, ferrets, cats, pigs, sheep, and humans, with a main goal of comparing gland secretion in control and CFTR-deficient humans and animals.
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CITATIONS (12)
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