Departments of Bioengineering and Chemical Engineering, University of Washington, Seattle, Washington 98195.
J Biomed Mater Res A. 2018 Oct;106(10):2777-2788. doi: 10.1002/jbm.a.36460. Epub 2018 Sep 8.
Fibrinogen (Fg) adsorption is an important mechanism underlying cell adhesion to biomaterials and was the major focus of the author's research career. This article summarizes our work on Fg adsorption, with citations of related work as appropriate. The molecular properties of Fg that promote adsorption and cell adhesion will be described. In addition, the adsorption behavior of Fg from buffer, binary solutions with other proteins, and blood plasma will be discussed, including the Vroman effect. Studies of platelet adhesion to surfaces preadsorbed with blood plasmas selectively deficient in Fg, vitronectin (Vn), fibronectin (Fn), or von Willebrand's factor (vWf) will be reviewed. These studies clearly showed a major role for Fg in platelet adhesion under static conditions and both Fg and vWf for adhesion from flowing suspensions, but no significant role for Vn or Fn. However, it was also shown that platelet adhesion was poorly correlated with the total amount of adsorbed Fg, but very well correlated with the binding of antibodies specific to the cell binding domains of Fg. A brief overview of nonfouling surfaces for prevention of Fg adsorption will be given. A more extensive discussion of structural changes in Fg after its adsorption is included, including changes detected with both physicochemical and biological methods. A short discussion of the state of the art of structural determination of adsorbed proteins with computational methods is also given. A final section identifies Fg adsorption as the single most important event determining the biocompatibility of implants in soft tissue and in blood. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 2777-2788, 2018.
纤维蛋白原(Fg)吸附是细胞黏附于生物材料的重要机制,也是作者研究工作的主要重点。本文总结了作者在纤维蛋白原吸附方面的工作,并适当引用了相关工作。将描述促进吸附和细胞黏附的纤维蛋白原的分子特性。此外,还将讨论从缓冲液、与其他蛋白质的二元溶液和血浆中吸附纤维蛋白原的行为,包括 Vroman 效应。综述了血小板黏附于预先吸附有纤维蛋白原、玻连蛋白(Vn)、纤维连接蛋白(Fn)或血管性血友病因子(vWf)缺陷的血浆的表面的研究。这些研究清楚地表明,纤维蛋白原在静态条件下对血小板黏附起主要作用,纤维蛋白原和 vWf 在流动悬浮液中对黏附起作用,但 Vn 或 Fn 没有明显作用。然而,研究还表明,血小板黏附与吸附的纤维蛋白原总量相关性较差,但与针对纤维蛋白原细胞结合结构域的抗体结合相关性非常好。本文简要概述了用于防止纤维蛋白原吸附的非缠结表面。还包括了纤维蛋白原吸附后结构变化的更广泛讨论,包括使用物理化学和生物学方法检测到的变化。还简要讨论了使用计算方法确定吸附蛋白质结构的最新技术。最后一部分将纤维蛋白原吸附确定为决定软组织和血液中植入物生物相容性的唯一最重要事件。© 2018 威利父子公司