Fluid movement between airspace and vascular compartments is important in normal lung function and pulmonary edema. This proposal is focused on biophysical (aim 1) and molecular (aim 2) water transporting mechanisms, and the role of molecular water channels in lung physiology (aim 3). The proposal consists of three specific aims:
In Specific Aim 1 they will apply novel optical methods to measure water permeability in intact lung epithelia, endothelia and individual cell membranes. Optical methods were developed in their laboratories to measure: a) airspace-to-capillary osmotic water permeability (Pf) in intact lung; b) transepithelial Pf in airways; and c) membrane Pf in epithelial layers. New optical approaches will be applied to quantify the role of epithelial vs. endothelial barriers in airspace-to-capillary water movement, of type I vs. type II cells in transalveolar water permeability, and of apical vs. basolateral Pf in airway and alveolar epithelia.
In Specific Aim 2 they will identify and characterize molecular water channels (aquaporins) that confer high water permeability in lung. Four aquaporins are expressed in lung: AQP3 (trachea) and AQP4 (airway basolateral membrane), cloned by the principal investigator, AQP1 (endothelium) and AQP5 (alveolar apical membrane) cloned by Dr. Agre. Water channels have not been identified at the alveolar basolateral membrane and airway apical membrane. The following cloning strategies will be used to identify these proteins: PCR-homology cloning using mRNA from alveolar and airway cells, and chromosome-specific exon amplification. Water channels will be studied by Xenopus oocyte expression and immunocytochemistry.
In Specific Aim 3 they will define the role of water channels in lung physiology using transgenic knock-out mice. The investigators recently generated the first animal knock-out models for water channels AQP4 and AQP1 deficient mice. Homozygous transgenic knock-out mice will be generated for AQP3 and AQP5, and characterized in terms of gross phenotype, lung water permeability, clearance of alveolar and interstitial edema, and airway resistance and reactivity.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL059198-05
Application #
6527131
Study Section
Special Emphasis Panel (ZRG2-RAP (01))
Program Officer
Gail, Dorothy
Project Start
1998-09-01
Project End
2004-08-31
Budget Start
2002-09-01
Budget End
2004-08-31
Support Year
5
Fiscal Year
2002
Total Cost
$286,986
Indirect Cost
Name
University of California San Francisco
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Tradtrantip, Lukmanee; Yangthara, Buranee; Padmawar, Prashant et al. (2009) Thiophenecarboxylate suppressor of cyclic nucleotides discovered in a small-molecule screen blocks toxin-induced intestinal fluid secretion. Mol Pharmacol 75:134-42
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Tradtrantip, Lukmanee; Tajima, Masato; Li, Lihua et al. (2009) Aquaporin water channels in transepithelial fluid transport. J Med Invest 56 Suppl:179-84
Ruiz-Ederra, Javier; Verkman, A S (2009) Aquaporin-1-facilitated keratocyte migration in cell culture and in vivo corneal wound healing models. Exp Eye Res 89:159-65
Magzoub, Mazin; Zhang, Hua; Dix, James A et al. (2009) Extracellular space volume measured by two-color pulsed dye infusion with microfiberoptic fluorescence photodetection. Biophys J 96:2382-90
Haggie, Peter M; Verkman, A S (2009) Defective organellar acidification as a cause of cystic fibrosis lung disease: reexamination of a recurring hypothesis. Am J Physiol Lung Cell Mol Physiol 296:L859-67

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