The broad, long-term objectives of the applicant are to define the roles of fibrinogen in hemostasis and thrombosis. This proposal addresses the issue of fibrin clot strength, a critical factor in the outcome of fibrinolytic therapy. Recent findings indicate that the minor gamma chain variant of fibrinogen binds directly to the zymogen form of factor XIII, a transglutaminase that stabilizes fibrin clots, and that the gamma variant serves as a carrier protein for factor XIII. This carrier function is likely to modulate the strength of the fibrin clot and its resistance to lysis by increasing the local concentration of factor XIII at the clot.
The specific aims of this proposal are to: I) Determine the role of y fibrinogen in modulating the strength of fibrin clots. This will be accomplished by measuring the rate and extent of gamma and gamma~ multimer formation, and by measuring the incorporation of alpha2-plasmin inhibitor into the clot. In addition, the effect of a synthetic peptide corresponding to the gamma~ extension, VRPEHPAETEYDSLYPEDDL, on lot lysis rates will be measured, as well as the IC50 of the peptide on gamma~ fibrinogen/factor XIII complex formation. The binding of gamma~ fibrinogen to both activated and unactivated factor XIII will also be measured to see if thrombin activation affects factor XIII binding to gamma~ fibrinogen. II) Identify the critical amino acids in the gamma~ chain that mediate factor XIII binding. This will be accomplished by measuring the equilibrium association constant of recombinant gamma~ fibrinogen mutants with factor XIII, particularly mutants in the sulfated Tyr residues at positions gamma~418 and gamma~422. In addition, alanine-scanning substitutions will be introduced throughout the twenty amino acid gamma~ chain extension to map the critical binding residues. III) Identify the peptide sequences in factor XIII that bind to the gamma~ chain. This will be accomplished by binding proteolyzed factor XIII subunits to a resin of immobilized gamma~ peptide to identify the binding peptide fragment(s). The results from the experiments in this proposal should provide new knowledge about the process of blood coagulation that may lead to way of modulating fibrin clot stability and clot lysis in vivo.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29HL053997-05
Application #
6184404
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1997-04-01
Project End
2002-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
5
Fiscal Year
2000
Total Cost
$105,790
Indirect Cost
Name
Oregon Health and Science University
Department
Pathology
Type
Schools of Medicine
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239
Lovely, Rehana S; Falls, Lisa A; Al-Mondhiry, Hamid A et al. (2002) Association of gammaA/gamma' fibrinogen levels and coronary artery disease. Thromb Haemost 88:26-31
Moaddel, M; Farrell, D H; Daugherty, M A et al. (2000) Interactions of human fibrinogens with factor XIII: roles of calcium and the gamma' peptide. Biochemistry 39:6698-705
Dallabrida, S M; Falls, L A; Farrell, D H (2000) Factor XIIIa supports microvascular endothelial cell adhesion and inhibits capillary tube formation in fibrin. Blood 95:2586-92
Moaddel, M; Falls, L A; Farrell, D H (2000) The role of gamma A/gamma ' fibrinogen in plasma factor XIII activation. J Biol Chem 275:32135-40
Dallabrida, S M; De Sousa, M A; Farrell, D H (2000) Expression of antisense to integrin subunit beta 3 inhibits microvascular endothelial cell capillary tube formation in fibrin. J Biol Chem 275:32281-8