Project II, 'Regulation of ENaC by Proteases and SGK1', has as its long-term objective the betterunderstanding of the molecular mechanisms that link the rate of Na+ absorption by airway epithelia tophysical conditions on the airway surface. Relevance to the mission of the agency is that the airway surfaceis the largest interface between the body and the outside environment, and the airway must continuously ridits surface of inhaled particulates. To do so, it has strongly conserved processes for regulating the height ofthe thin film of liquid on its surface. Excessive Na+ absorption mediated by airway epithelial Na+ channels(ENaC) contributes to lung disease in cystic fibrosis patients, but the mechanisms that normally restrainENaC are poorly defined. To better understand how respiratory pathogens and/or inhaled chemicals couldupset normal regulation in the airways, we propose to examine the regulation of ENaC by two pathways thatmay link the rate of Na+ absorption to stimuli present on the airway surface. The Project has thee aims.
Aim1 : Extracellular proteolytic activity, as either soluble proteases, such as neutrophil elastase, or endogenoussurface proteases, probably CAP1 (prostasin), stimulate near silent Po approx. 0.01) ENaC to become active(Po approx 0.5). Protease inhibitors, though essential for the model, are not addressed in this Project, whichfocuses on the molecular mechanism of proteolytic regulation.
Aim 2 : The role of ENaC surface density andturnover in airway health and disease is unknown.
Aim 2 tests the effects of SGK1, ATP, and proteases onENaC surface density and turnover.
Aim 3 explores protease regulation of airway surface liquid volume inhighly differentiated human airway cells in vitro and in a mouse model, in vivo. Our studies are focused onthe effects of local signals on the open probability and surface density of ENaC, and how these modes ofregulating Na+ transport satisfy the airway's requirement for tonic volume absorption, while preserving itsability to accelerate or slow the process as conditions on the airway surface require. Relevance to PublicHealth: This research is designed to study the physiologic processes responsible for clearing inhaledparticles from the surface of the airways, so that the airways are able to deliver fresh air to the lungs' gasexchange surface.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL034322-21A1
Application #
7215375
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2006-12-01
Project End
2012-01-31
Budget Start
2006-12-01
Budget End
2008-01-31
Support Year
21
Fiscal Year
2007
Total Cost
$402,480
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
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