The overall goal is to understand how the lung regulates surfactant pools in health and disease. The hypothesis is that alveolar surfactant is regulated by cytokines/growth factors/hormones and that studies of surfactant metabolism and function in transgenic mice with abnormalities in these systems will provide insights into surfactant homeostasis. Although there is considerable information about the overall kinetics of metabolism of the major surfactant components - saturated phosphatidylcholine (Sat PC) and the surfactant associated SP-A, SP-B and SP-C, the relative contributions of type II cells, Clara cells, and macrophages to alveolar metabolism is not known. The contributions of these cell types to the metabolism will be evaluated in normal mice. Transgenic mice with alveolar proteinosis (GM-CSF-I-,IL-4 overexpression) and pulmonary fibrosis (TGFalpha overexpression) will be used to identify the metabolic pathway(s) and/or cell types responsible for the abnormalities in surfactant homeostasis. Measurements will be made of precursor incorporation into Sat PC and the surfactant proteins, secretion and alveolar and lung clearances of these surfactant components. Surfactants of abnormal composition resulting from transgenic constructs that lack SP-A or SP-D, overexpress SP-A, and overexpress SP-A and SP-B will be evaluated for in vitro biophysical properties and function to learn the ranges of surfactant function consistent with relatively normal lung function. Because the abnormalities in surfactant in these transgenic mice are similar to those encountered in patients with alveolar proteinosis, pulmonary fibrosis, other lung injuries and bronchopulmonary dysplasia, the results will provide a framework to understand surfactant metabolic abnormalities in human lung diseases.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD011932-22
Application #
2888841
Study Section
Human Embryology and Development Subcommittee 1 (HED)
Program Officer
Wright, Linda
Project Start
1977-09-30
Project End
2003-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
22
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
Ikegami, Machiko; Dhami, Rajwinder; Schuchman, Edward H (2003) Alveolar lipoproteinosis in an acid sphingomyelinase-deficient mouse model of Niemann-Pick disease. Am J Physiol Lung Cell Mol Physiol 284:L518-25
Glasser, Stephan W; Detmer, Emily A; Ikegami, Machiko et al. (2003) Pneumonitis and emphysema in sp-C gene targeted mice. J Biol Chem 278:14291-8
Gurel, O; Ikegami, M; Chroneos, Z C et al. (2001) Macrophage and type II cell catabolism of SP-A and saturated phosphatidylcholine in mouse lungs. Am J Physiol Lung Cell Mol Physiol 280:L1266-72
Kramer, B W; Jobe, A H; Ikegami, M (2001) Exogenous surfactant changes the phenotype of alveolar macrophages in mice. Am J Physiol Lung Cell Mol Physiol 280:L689-94
Rider, E D; Ikegami, M; Pinkerton, K E et al. (2000) Lysosomes from rabbit type II cells catabolize surfactant lipids. Am J Physiol Lung Cell Mol Physiol 278:L68-74
Ikegami, M; Whitsett, J A; Chroneos, Z C et al. (2000) IL-4 increases surfactant and regulates metabolism in vivo. Am J Physiol Lung Cell Mol Physiol 278:L75-80
Elhalwagi, B M; Zhang, M; Ikegami, M et al. (1999) Normal surfactant pool sizes and inhibition-resistant surfactant from mice that overexpress surfactant protein A. Am J Respir Cell Mol Biol 21:380-7
Jobe, A H; Ikegami, M (1998) Surfactant homeostasis in corticotropin-releasing hormone deficiency in adult mice. Am J Respir Crit Care Med 158:995-7
Ikegami, M; Korfhagen, T R; Whitsett, J A et al. (1998) Characteristics of surfactant from SP-A-deficient mice. Am J Physiol 275:L247-54
Ikegami, M; Horowitz, A D; Whitsett, J A et al. (1998) Clearance of SP-C and recombinant SP-C in vivo and in vitro. Am J Physiol 274:L933-9

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