The control of endothelial motility on molecularly engineered surfaces may be an important step in the development of a biologically functional small diameter arterial prosthesis. We believe that mimicking features of cell contact mediated migration in self-assembling bioorganic films provides a rational design strategy for such an approach. Specifically, we intend to: (1) Synthesize and characterize composite lipid films as substrates for controlled endothelial migration. Integrin and glycosaminoglycan (GAG) binding oligopeptide ligands will be synthesized and used as pendant groups on phospholipid macromolecules. A GAG-lipid conjugate, based upon heparan sulphate, will also be synthesized as a molecular sink for basic Fibroblast Growth Factor (bFGF). Atomic level properties and film biostability characteristics will be investigated by vibrational spectroscopy and scanning probe microscopy. (2) Define the structural and chemical features of membrane-mimetic surfaces which modulate endothelial cell motility. Human endothelial cell adhesion and migration will be studied as a function of ligand type, density, and distribution. Likewise, the ability of bFGF, incorporated into supramolecular lipid assemblies, to enhance motility will be analyzed and related to its surface concentration and dissociation kinetics. (3) Characterize the biomimetic material properties which influence thromboresistance and spontaneous endothelialization in vivo. A self-expanding polymeric endovascular prosthesis, as a tool for initial in vivo investigations, will be fabricated, functionalized with a biomimetic film, and surface properties characterized. Acute platelet and fibrinogen deposition will be studied in a baboon ex vivo shunt model followed by characterizing endothelial responses in a limited series of primate implant studies.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29HL056819-02
Application #
2445355
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1996-07-01
Project End
2000-06-30
Budget Start
1997-07-01
Budget End
1998-06-30
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Emory University
Department
Surgery
Type
Schools of Medicine
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Dydek, E Victoria; Chaikof, Elliot L (2016) Simulated Thrombin Generation in the Presence of Surface-Bound Heparin and Circulating Tissue Factor. Ann Biomed Eng 44:1072-84
Jordan, S W; Chaikof, E L (2011) Simulated surface-induced thrombin generation in a flow field. Biophys J 101:276-86