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力谱法探究纤维蛋白原基质非粘性特性的起源。

Origin of the nonadhesive properties of fibrinogen matrices probed by force spectroscopy.

机构信息

Center for Metabolic Biology and School of Life Sciences, Arizona State University, Tempe, Arizona 85287, United States.

出版信息

Langmuir. 2010 Nov 16;26(22):17269-77. doi: 10.1021/la101791r. Epub 2010 Sep 30.

Abstract

The deposition of a multilayered fibrinogen matrix on various surfaces results in a dramatic reduction of integrin-mediated cell adhesion and outside-in signaling in platelets and leukocytes. The conversion of a highly adhesive, low-density fibrinogen substrate to the nonadhesive high-density fibrinogen matrix occurs within a very narrow range of fibrinogen coating concentrations. The molecular events responsible for this transition are not well understood. Herein, single-cell and molecular force spectroscopy were used to determine the early steps in the formation of nonadhesive fibrinogen substrates. We show that the adsorption of fibrinogen in the form of a molecular bilayer coincides with a several-fold reduction in the adhesion forces generated between the AFM tip and the substrate as well as between a cell and the substrate. The subsequent deposition of new layers at higher coating concentrations of fibrinogen results in a small additional decrease in adhesion forces. The poorly adhesive fibrinogen bilayer is more extensible under an applied tensile force than is the surface-bound fibrinogen monolayer. Following chemical cross-linking, the stabilized bilayer displays the mechanical and adhesive properties characteristic of a more adhesive fibrinogen monolayer. We propose that a greater compliance of the bi- and multilayer fibrinogen matrices has its origin in the interaction between the molecules forming the adjacent layers. Understanding the mechanical properties of nonadhesive fibrinogen matrices should be of importance in the therapeutic control of pathological thrombosis and in biomaterials science.

摘要

在各种表面上沉积多层纤维蛋白原基质会导致血小板和白细胞中整合素介导的细胞黏附和细胞外信号显著减少。高度黏附的低密度纤维蛋白原底物转化为非黏附的高密度纤维蛋白原基质的过程发生在纤维蛋白原涂层浓度的非常窄的范围内。导致这种转变的分子事件还不是很清楚。在此,单细胞和分子力谱被用于确定非黏附纤维蛋白原底物形成的早期步骤。我们表明,纤维蛋白原的分子双层吸附与 AFM 针尖与基底之间以及细胞与基底之间产生的黏附力的几倍降低同时发生。随后在更高纤维蛋白原涂层浓度下沉积新层会导致黏附力的微小额外降低。在施加的拉伸力下,较差的纤维蛋白原双层比表面结合的纤维蛋白原单层更具可伸展性。交联后,稳定的双层显示出与更具黏附性的纤维蛋白原单层特征一致的力学和黏附特性。我们提出,双和多层纤维蛋白原基质的更大顺应性源于形成相邻层的分子之间的相互作用。了解非黏附纤维蛋白原基质的力学性能对于病理性血栓形成的治疗控制和生物材料科学都很重要。

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