Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.
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ABSTRACT: While pathological and clinical data suggest that small airways are involved in early cystic fibrosis (CF) lung disease development, little is known about how the lack of cystic fibrosis transmembrane conductance regulator (CFTR) function contributes to disease pathogenesis in these small airways. Large and small airway epithelia are exposed to different airflow velocities, temperatures, humidity, and CO2 concentrations. The cellular composition of these two regions is different, and small airways lack submucosal glands. To better understand the ion transport properties and impacts of lack of CFTR function on host defense function in small airways, we adapted a novel protocol to isolate small airway epithelial cells from CF and non-CF pigs and established an organotypic culture model. Comp
SUBMITTER: Li X
PROVIDER: S-EPMC4824164 | biostudies-literature | 2016 Apr
REPOSITORIES: biostudies-literature
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