This is a Program Project entitled 'The Biological Basis for Perinatal Transition' which reflects our interest in the development of the mammalian fetus and its transition to postnatal life. We view the postconceptual development of the mammalian fetus as characterized by several critical themes: organogenesis, regulation of somatic growth, maturation of key endocrine axes, and preparation for postnatal life. Development emphasizes these themes by progression through a series of only partially understood, but carefully choreographed, maturational steps. Each process significantly impacts the outcome of subsequent milestones. For example, the ontogeny of the fetal hypothalamic- pituitary-adrenocortical axis has been extensively studied. In mammalian fetal development an increase in late gestation in the production of cortisol is a key hormonal trigger for maturation of many key organ systems and other hormonal axes. The role of insulin in regulating late gestation fetal liver growth and functional differentiation is another example. In contrast, placental differentiation and syncytiotrophoblast formation is largely under the influence of maternal hormonal factors. In all cases, perturbation of these mechanisms has pathophysiologic consequences for the fetus and newborn which are relevant to clinical conditions. This Program Project Grant will support research designed to define how several of these events impact fetal and newborn development. We will study as model systems: the factors which regulate proliferation and differentiation of developing the trophoblast factors which regulate the growth and proliferation of fetal and neonatal hepatocytes; unique mechanisms for hormonal regulation of gene transcription between fetal and adult life; the role of glucocorticoids in the regulation of critical aspects of brain maturation.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
5P01HD011343-20
Application #
2403065
Study Section
Maternal and Child Health Research Committee (HDMC)
Project Start
1977-12-01
Project End
2001-06-30
Budget Start
1997-07-01
Budget End
1998-06-30
Support Year
20
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Women and Infants Hospital-Rhode Island
Department
Type
DUNS #
069851913
City
Providence
State
RI
Country
United States
Zip Code
02905
Wadhawan, Rajan; Tseng, Yi-Tang; Stabila, Joan et al. (2003) Regulation of cardiac beta 1-adrenergic receptor transcription during the developmental transition. Am J Physiol Heart Circ Physiol 284:H2146-52
Tseng, Yi-Tang; Wadhawan, Rajan; Stabila, Joan P et al. (2002) Molecular interactions between glucocorticoid and catecholamine signaling pathways. J Allergy Clin Immunol 110:S247-54
Tseng, Y T; Kopel, R; Stabila, J P et al. (2001) Beta-adrenergic receptors (betaAR) regulate cardiomyocyte proliferation during early postnatal life. FASEB J 15:1921-6
McNab, T C; Tseng, Y T; Stabila, J P et al. (2001) Liganded and unliganded steroid receptor modulation of beta 1 adrenergic receptor gene transcription. Pediatr Res 50:575-80
Tseng, Y T; Stabila, J P; Nguyen, T T et al. (2001) A novel glucocorticoid regulatory unit mediates the hormone responsiveness of the beta1-adrenergic receptor gene. Mol Cell Endocrinol 181:165-78
Tseng, Y T; Stabila, J; McGonnigal, B et al. (1998) An inverted cAMP response element mediates the cAMP induction of the ovine beta 1-adrenergic receptor gene. Biochem Mol Biol Int 46:1127-34