Leukocytes, when exposed to activating stimuli, are capable of a wide variety of responses that are important in coagulation events. The interactions of these cells with other blood components such as proteins, blood factors, and platelets affect the amount of thrombus formation that occurs after damage to the vascular system. The biomaterial-blood interaction also initiates a series of coagulation events that result in artificial surface-induced thrombosis. Although extensive research has been done to determine the role of platelets and proteins in thrombus formation and embolization, there has been only limited study of how leukocytes modulate these responses. We propose to investigate the role of peripheral blood leukocytes in blood-material interactions in vitro by exposing the cells te biomaterials which have markedly different surface properties. The leukocyte responses of adherence, phagocytosis, degranulation, and expression of procoagulant and fibrinolytic activity will be assessed. In addition, the activation of complement by biomaterials, and subsequent leukocyte aggregation will be investigated. In parallel experiments, plasma proteins which have been shown to be relevant to biomaterial thrombogenicity will be preadsorbed onto the polymer surfaces before exposure to leukocytes to examine their effect on the leukocyte response. Leukocyte interactions with platelets as a result of arachidonic acid metabolism will be investigated to determine the role of this metabolite in the cellular enhancement of thrombogenesis. Canine ex vivo experiments will provide information about the acute and chronic reaction of leukocytes to implantation of a polymer material through measurement of leukocyte deposition and morphology. These studies of leukocyte responses and thrombus formation will lead to a better understanding of the mechanisms involved in artificial surface-induced thrombogenesis and will aid in the design of improved biocompatible polymeric materials.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL047179-05
Application #
2223474
Study Section
Special Emphasis Panel (SRC (MM))
Project Start
1991-08-01
Project End
1996-04-30
Budget Start
1994-09-01
Budget End
1996-04-30
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Delaware
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
059007500
City
Newark
State
DE
Country
United States
Zip Code
19716
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Yung, L Y; Colman, R W; Cooper, S L (1999) Neutrophil adhesion on polyurethanes preadsorbed with high molecular weight kininogen. Blood 94:2716-24
Khan, M M; Kunapuli, S P; Lin, Y et al. (1998) Three noncontiguous peptides comprise binding sites on high-molecular-weight kininogen to neutrophils. Am J Physiol 275:H145-50
Yung, L Y; Cooper, S L (1998) Neutrophil adhesion on phosphorylcholine-containing polyurethanes. Biomaterials 19:31-40
Yung, L Y; Lim, F; Khan, M M et al. (1996) Neutrophil adhesion on surfaces preadsorbed with high molecular weight kininogen under well-defined flow conditions. Immunopharmacology 32:19-23
Lim, F; Cooper, S L (1995) Effect of sulphonate incorporation on in vitro leucocyte adhesion to polyurethanes. Biomaterials 16:457-66
Silver, J H; Hergenrother, R W; Lin, J C et al. (1995) Surface and blood-contacting properties of alkylsiloxane monolayers supported on silicone rubber. J Biomed Mater Res 29:535-48
Silver, J H; Myers, C W; Lim, F et al. (1994) Effect of polyol molecular weight on the physical properties and haemocompatibility of polyurethanes containing polyethylene oxide macroglycols. Biomaterials 15:695-704
Lin, H B; Sun, W; Mosher, D F et al. (1994) Synthesis, surface, and cell-adhesion properties of polyurethanes containing covalently grafted RGD-peptides. J Biomed Mater Res 28:329-42
Lin, H B; Lewis, K B; Leach-Scampavia, D et al. (1993) Surface properties of RGD-peptide grafted polyurethane block copolymers: variable take-off angle and cold-stage ESCA studies. J Biomater Sci Polym Ed 4:183-98

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