The dramatic cellular changes that take place during heart development are the result of the expression and interaction of several morphogenetic factors. At critical times in heart development, such as looping, septation, trabeculation, and valve formation, these factors play a significant role in determining the form and function of the developing heart. Fundamental events necessary for heart development include the expression of extracellular matrix (ECM) components, arrangement and remodeling of ECM, attachment of the ECM to cellular components, and the formation of cell:cell contacts. The proposed investigations will focus on the interaction between ECM components and specific cell surface receptors of the differentiating cellular components of the heart. Specifically we will examine: 1) the expression of integrins and cadherins at different stages of heart development; 2) the expression of basement membrane components during development by cardiac myocytes and their possible role in differentiation of the heart; and 3) the role of growth factors/cytokines on the regulation of integrins, cadherins and collagenases during cardiac development. Several experimental approaches will be used to analyze these specific aims including: A) 3-dimensional collagen gel cultures to examine the effects of growth factors/cytokines on expression of ECM components, their specific receptors and metalloproteases; B) cell migration, cell-cell interaction with aggregate formation in rotation culture, and cell:ECM adhesion assays to determine the role of potential regulatory components; C) microinjection of whole embryo cultures and individual cells to determine the effects of regulatory components at specific stages of development; D) morphological and morphometric analysis of immunolocalization of specific regulatory components and their receptors during critical stages of development; and E) analysis of the biochemical and molecular expression of regulatory components in collagen gels, embryo culture compared to in vivo development. These experimental approaches will allow for the analysis of the regulation of the morphogenetic events associated with normal heart development and provide essential data on the mechanisms involved in congenital heart defects.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL037669-09
Application #
2218532
Study Section
Human Embryology and Development Subcommittee 1 (HED)
Project Start
1986-09-30
Project End
1998-05-31
Budget Start
1995-09-15
Budget End
1998-05-31
Support Year
9
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of South Carolina at Columbia
Department
Pathology
Type
Schools of Medicine
DUNS #
111310249
City
Columbia
State
SC
Country
United States
Zip Code
29208
Morales, Mary O; Price, Robert L; Goldsmith, Edie C (2005) Expression of Discoidin Domain Receptor 2 (DDR2) in the developing heart. Microsc Microanal 11:260-7
Borg, Thomas K (2004) It's the matrix! ECM, proteases, and cancer. Am J Pathol 164:1141-2
Goldsmith, Edie C; Carver, Wayne; McFadden, Alex et al. (2003) Integrin shedding as a mechanism of cellular adaptation during cardiac growth. Am J Physiol Heart Circ Physiol 284:H2227-34
Sussman, Mark A; McCulloch, Andrew; Borg, Thomas K (2002) Dance band on the Titanic: biomechanical signaling in cardiac hypertrophy. Circ Res 91:888-98
Goldsmith, Edie C; Borg, Thomas K (2002) The dynamic interaction of the extracellular matrix in cardiac remodeling. J Card Fail 8:S314-8
Knezevic, V; Sim, A J; Borg, T K et al. (2002) Isotonic biaxial loading of fibroblast-populated collagen gels: a versatile, low-cost system for the study of mechanobiology. Biomech Model Mechanobiol 1:59-67
Ross, R S; Borg, T K (2001) Integrins and the myocardium. Circ Res 88:1112-9
Ding, B; Price, R L; Goldsmith, E C et al. (2000) Left ventricular hypertrophy in ascending aortic stenosis mice: anoikis and the progression to early failure. Circulation 101:2854-62
Yost, M J; Simpson, D; Wrona, K et al. (2000) Design and construction of a uniaxial cell stretcher. Am J Physiol Heart Circ Physiol 279:H3124-30
Kanekar, S; Borg, T K; Terracio, L et al. (2000) Modulation of heart fibroblast migration and collagen gel contraction by IGF-I. Cell Adhes Commun 7:513-23

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