Project V is based on the overall hypothesis that normal lung defense mechanisms depend on the integrated actions of airway epithelia to regulate the volume and composition of airway secretions and mucociliary clearance. The project proposes to study the concept that the epithelial purinergic receptor for triphosphate nucleotides (P2U-R), coupled to the autocrine actions of ATP on the airway surface, plays a key role in the coordination of the cellular activities required to promote efficient mucociliary clearance, including ion transport, mucin secretion, and ciliary beat frequency. This proposal will also study functional and molecular aspects of key ion transport components, i.e., epithelial Na+ channels (ENaC) and Cl- transport pathways, including cAMP-mediated (CFTR) Cl- channels and Ca2+-activated """"""""alternative"""""""" Cl- channels (Cl-/a), of the airway epithelia.
The Specific Aims i nclude: 1) defining quantitative relationships between CFTR expression and function and epithelial phenotype (health and disease); 2) characterizing the expression and regulation of airway ENaC in normal subjects, and testing the hypothesis that abnormal expression and/or regulation of ENaC produces airways disease; and 3) testing the hypothesis that there is an ATP/P2U-R autocrine/paracrine system in airways, and that it is a target for novel therapies. The research strategy will emphasize studies of human tissue and in vivo studies of humans, including normal subjects and patients with cystic fibrosis, chronic bronchitis, primary ciliary dyskinesia, Liddle's syndrome (genetic defects in beta-ENaC), and pseudohypoaldosteronism (defect of mineralocorticoid-mediated Na+ transport). The protocols involve in vivo physiologic studies of Na+ and Cl- transport, and the ATP/P2U-R system. Molecular techniques that were developed to estimate the level of steady-state CFTR mRNA (quantitative RT-PCR and RPA) in nasal epithelia obtained by scrape biopsy will be extended to study the expression of ENaC subunits (alpha, beta, gamma) and P2U-R. The presence of ATP and its metabolism in airways of normal subjects and patients with airways diseases will be determined by luminometry and HPLC. Aerosolized UTP may be useful for the treatment of CF, and perhaps other airways disease, and we will test for homologous and heterologous desensitization of P2U-R in vivo approaches. Insights from these studies will clearly contribute to better understanding of normal airway epithelial physiology and the pathogenesis of inherited and acquired airways diseases, and facilitate the development of novel therapies.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL034322-11A1
Application #
5213545
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
11
Fiscal Year
1996
Total Cost
Indirect Cost
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