The theme of this SCOR proposal is Normal and Disordered Growth and Development of Respiratory Systems. It represents a continuation of a Pediatric Pulmonary SCOR (now in year 14) which in the past has focused on lung infections and their consequences on airways growth and development. The proposal includes two projects which continue previous SCOR studies and 5 new projects which address in greater depth the molecular mechanisms of airways development, injury and repair, and regulation of airway tone. Four core services (Administrative, Molecular Biology, Morphology/Ultrastructure and Microbiology/Immunology) will support these projects. The first four projects constitute a subgroup which explores molecular aspects of ciliated (Project II) and secretory (Project III) cell differentiation in large airways, response of these cells to injury, and mechanisms which may play a role in development and repair of this epithelium, i.e., growth factors (Project I) and cell-cell communication through gap junctions (Project IV). These studies will rely heavily on the postnatal ferret trachea as a developmental and injury model, but will examine human tissue and use a range of experimental models from primary cultures of epithelial cells to transgenic animals that overexpress and underexpress IGF-I in order to probe the molecular events attending normal development and repair. Previous SCOR studies have identified the attachment protein (PI) of Mycoplasma pneumoniae and F glycoprotein of respiratory syncytial virus (RSV) as important immunogens. Project IV proposes to clone these genes into an adenovirus to produce a live oral vaccine for the prevention of mycoplasma infection. We anticipate that these coordinated and interactive studies will provide essential basic and applied information that will be used to 1) better understand the origins and course of childhood obstructive airways disease and apnea and 2) develop improved therapeutic and preventive approaches to these problems.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
5P50HL019171-19
Application #
2215237
Study Section
Special Emphasis Panel (SRC (MA))
Project Start
1991-12-30
Project End
1996-11-30
Budget Start
1994-12-01
Budget End
1995-11-30
Support Year
19
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Pediatrics
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Price, Wayne A; Moats-Staats, Billie M; Stiles, Alan D (2002) Pro- and anti-inflammatory cytokines regulate insulin-like growth factor binding protein production by fetal rat lung fibroblasts. Am J Respir Cell Mol Biol 26:283-9
Gordon, Phillip V; Moats-Staats, Billie M; Stiles, Alan D et al. (2002) Dexamethasone changes the composition of insulin-like growth factor binding proteins in the newborn mouse ileum. J Pediatr Gastroenterol Nutr 35:532-8
Gordon, P V; Marshall, D D; Stiles, A D et al. (2001) The clinical, morphologic, and molecular changes in the ileum associated with early postnatal dexamethasone administration: from the baby's bowel to the researcher's bench. Mol Genet Metab 72:91-103
Gordon, P V; Price, W A; Stiles, A D et al. (2001) Early postnatal dexamethasone diminishes transforming growth factor alpha localization within the ileal muscularis propria of newborn mice and extremely low-birth-weight infants. Pediatr Dev Pathol 4:532-7
Stiles, A D; Chrysis, D; Jarvis, H W et al. (2001) Programmed cell death in normal fetal rat lung development. Exp Lung Res 27:569-87
Gordon, P V; Price, W A; Stiles, A D (2001) Dexamethasone administration to newborn mice alters mucosal and muscular morphology in the ileum and modulates IGF-I localization. Pediatr Res 49:93-100
Moats-Staats, B M; Jarvis, H W; Brighton, B et al. (2000) Regulation of the rat BB1 RNA during normal rat lung development. Exp Lung Res 26:401-20
Gordon, P; Rutledge, J; Sawin, R et al. (1999) Early postnatal dexamethasone increases the risk of focal small bowel perforation in extremely low birth weight infants. J Perinatol 19:573-7
Price, W A; Moats-Staats, B M; Sekhon, H S et al. (1998) Expression of the insulin-like growth factor system in postpneumonectomy lung growth. Exp Lung Res 24:203-17
Veness-Meehan, K A; Moats-Staats, B M; Maniscalco, W M et al. (1997) Changes in decorin expression with hyperoxic injury to developing rat lung. Pediatr Res 41:464-72

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