Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3029832 | Thrombosis Research | 2007 | 8 Pages |
Abstract
We have previously reported that a recombinant protein (Mr 47Â kDa), which contains both active peptide of platelet receptors for types I and III collagen inhibits both types I and III collagen-induced platelet aggregation. In order to eliminate non-reactive portion of the protein, we have constructed a recombinant of rHyB (Mr 6Â kDa). In addition, we chemically synthesized a hybrid peptide with 30 amino acid residues (cHyB, Mr 3Â kDa) that contains each of the active peptide derived from platelet receptors for types I and III collagen and a linker of 12 amino acid residues. In the present investigation, we report that both rHyB and cHyB inhibit type I and type III collagen-induced platelet aggregation, and the adhesion of radiolabeled platelets onto rabbit aortic segments in a dose-dependent manner. We have used an animal model, which employs FeCl3 to induce thrombi formation to study the effectiveness of both rHyb and cHyB on preventing thrombi formation. We obtained results that show that both rHyB and cHyB can inhibit thrombi formation in a dose-dependent manner. These results suggest that either rHyB or cHyB may be a possible therapeutic agent in preventing thrombi formation.
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Authors
Haiming Du, Janice A. Zawaski, M. Waleed Gaber, Thomas M. Chiang,