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
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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