Coating conditions matter to collagen matrix formation regarding von Willebrand factor and platelet binding |
| |
Authors: | Mendelboum Raviv Shlomit Szekeres-Csiki Katalin Jenei Attila Nagy Janos Shenkman Boris Savion Naphtali Harsfalvi Jolan |
| |
Affiliation: | a Clinical Research Center, Medical and Health Science Center, University Debrecen, Hungaryb Department of Biophysics and Cell Biology, Medical and Health Science Center, University Debrecen, Hungaryc Amalia Biron Research Institute of Thrombosis and Hemostasis, Sheba Medical Center, Tel-Hashomer, Tel Aviv University, Tel Aviv, Israeld Eye Research Institute, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel |
| |
Abstract: | IntroductionVon Willebrand factor (VWF) and platelet binding needs a uniform collagen matrix therefore we aimed to find an optimal condition for the preparation of human type-I and type-III collagen matrices.MethodThe effects of pH, salt and ligand concentration and binding time were tested when collagen matrices were prepared by adsorption. Surface-bound collagen and collagen-bound VWF measured by specific antibodies. Platelet adhesion was tested under flow conditions at a shear rate of 1800 s− 1 for 2 min. Matrices and platelets were visualized by atomic force and scanning electron microscope.ResultsThe extent of human collagens type-I and III binding to the surface was 10 and 4 times greater and binding was maximal under 8-16 hours, when coated from physiological buffer solution versus acid solution. Collagen fibrils were more developed and platelet adhesion was higher, with more organized and denser aggregates. VWF binding was parallel to the surface bound collagen in both collagen types.ConclusionCollagen coating of surfaces for VWF binding and platelet adhesion studies is very variable from acid solution. Our experiments provide evidences that neutralizing the acid and adding NaCl in physiological concentration, thereby facilitating formation of collagen fibril molecules in solution, results in efficient coating of human type-I and type III collagens, which then bind normal VWF equally well. |
| |
Keywords: | AFM, atomic force microscopy SEM, scanning electron microscopy OD, optical density rOD, relative optical density PBS, phosphate buffered saline VWD, von Willebrand disorder/disease VWF, von Willebrand factor VWF:Ag, von Willebrand factor antigen VWF:CB, von Willebrand factor collagen binding GP, glycoprotein HRP, horseradish peroxidase SC, surface coverage AS, average size Kd, dissociation constant |
本文献已被 ScienceDirect PubMed 等数据库收录! |
|