Role of Integrins During Heart Valve Development

Project: Research project

Description

DESCRIPTION (provided by applicant): Cardiac endocardial cushion morphogenesis in the atrioventricular (AV) canal requires an epithelial-tomesenchymal cell transition (EMT) to form a population of cells that contribute to valve leaflet formation and cardiac septation. Abnormal AV canal development can result in a common, severe form of congenital heart disease, and computer modeling predicts these defects can result from altered cell adhesiveness. While considerable progress has been made in understanding how multiple families of growth factors regulate EMT, far less is known about how the interaction of cells with the surrounding ECM influences EMT. One important class of transmembrane receptors that link the ECM with intracellular signaling pathways is the integrin family of cell surface receptors. Although early studies demonstrated that an interaction of beta1 integrins with the ECM is required for AV canal EMT, almost nothing is known about which integrin heterodimers are involved or how they contribute to this important developmental event. We have found that cells from infants with heart valve defects display altered adhesion on collagen type VI, a component of the developing heart valve ECM. Importantly, we identified alpha 3 beta 1 integrin as the receptor mediating this process, and preliminary studies from our laboratory implicate an important role for this specific integrin receptor during AV canal EMT. These data lead to the central hypothesis that alpha 3 beta 1 integrin is required for AV canal development by forming a structural link to specific ECM ligands that necessary for cell migration, and by directing gene expression during EMT through beta 1 integrin-mediated intracellular signaling. This hypothesis will be tested by experiments that will determine alpha 3 integrin's role during AV canal EMT and define the beta 1 integrin-mediated signaling pathways that are required during heart valve development. These studies will contribute to our fundamental knowledge of the role of integrins in heart valve development and EMT. From a clinical perspective, this research is significant because 10% of all infants with heart defects are directly attributed to improper AV valve development.
StatusFinished
Effective start/end date4/1/042/28/09

Funding

  • National Institutes of Health: $329,288.00
  • National Institutes of Health: $348,949.00
  • National Institutes of Health: $318,930.00
  • National Institutes of Health: $339,079.00

Fingerprint

Heart Valves
Integrins
Integrin alpha3beta1
Integrin beta Chains
CD29 Antigens
Integrin alpha3
Endocardial Cushions
Collagen Type VI
Adhesiveness
Cell Surface Receptors
Morphogenesis
Cell Communication
Cell Movement
Heart Diseases
Intercellular Signaling Peptides and Proteins
Epithelial Cells
Ligands
Gene Expression
Research
Population

ASJC

  • Medicine(all)