MECHANISMS IN THE REMODELING OF LUNG STRUCTURE

Information

  • Research Project
  • 6526665
  • ApplicationId
    6526665
  • Core Project Number
    P01HL029594
  • Full Project Number
    5P01HL029594-20
  • Serial Number
    29594
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/1/1983 - 41 years ago
  • Project End Date
    8/31/2003 - 21 years ago
  • Program Officer Name
    CROXTON, THOMAS
  • Budget Start Date
    9/1/2002 - 22 years ago
  • Budget End Date
    8/31/2003 - 21 years ago
  • Fiscal Year
    2002
  • Support Year
    20
  • Suffix
  • Award Notice Date
    8/14/2002 - 22 years ago

MECHANISMS IN THE REMODELING OF LUNG STRUCTURE

This multidisciplinary program will utilize concepts and techniques of cell and molecular biology to investigate lung development, lung structure, alterations in lung structure due to inflammation, mechanisms of alveolar repair, and alveolar surface proteins. Our overall hypothesis is that extracellular matrix has a fundamental role in lung development and the preservation of normal lung architecture and function, and that disturbances in extracellular matrix are pivotal in emphysema, the acute respiratory disease syndrome, pulmonary fibrosis, chronic pulmonary hypertension, and other disorders in which lung structure is altered. In this program we will study: (1) alveolar basement membranes in lung development and disease; (2) alveolar surface proteins as factors in host defense; (3) matrix metalloproteinase expression by alveolar epithelium; (4) macrophage elastase in emphysema; and (5) pulmonary vascular development and remodeling. A number of molecules will receive emphasis, including laminin alpha chains, surfactant proteins A and D (SP-A and SP- D), cytokines (TNF-alpha, IL-1, IL-6), LPS binding protein, matrilysin, macrophage elastase, tropoelastin, fibrillin-2, microfibril-associated glycoprotein (MAGP), and latent TGF-beta/1-binding protein-2 (LTBP-2). The proposed studies will encompass lung cells in culture, embryonic lungs in culture, transgenic mice, rodent models of alveolar injury induced by hyperoxia, bleomycin, N-nitroso-N-methylurethane, and tobacco smoke, and interactions between SP-D, microorganisms, and macrophages. Human lung tissue and lung cells will be analyzed in some studies. A Morphology Core organized into Histology, Immunology, and Molecular Biology components will assist with tissue processing and diverse morphologic procedures, including 'in situ' hybridization and immunostaining, and will assist in the development of immunologic reagents. The Morphology Core will provide a center for correlative interactions among the investigators in their independent, yet complementary, studies of lung biology.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    P01
  • Administering IC
    HL
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    1423256
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    838
  • Ed Inst. Type
  • Funding ICs
    NHLBI:1423256\
  • Funding Mechanism
  • Study Section
    HLBP
  • Study Section Name
    Heart, Lung, and Blood Program Project Review Committee
  • Organization Name
    BARNES-JEWISH HOSPITAL
  • Organization Department
  • Organization DUNS
  • Organization City
    SAINT LOUIS
  • Organization State
    MO
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    63110
  • Organization District
    UNITED STATES