Velzenberger Elodie, Pezron Isabelle, Legeay Gilbert, Nagel Marie-Danielle, El Kirat Karim
Université de Technologie de Compiègne (UTC), BP 20529, 60205 Compiègne Cedex, France.
Langmuir. 2008 Oct 21;24(20):11734-42. doi: 10.1021/la801727p. Epub 2008 Sep 25.
The development of adhesive as well as antiadhesive surfaces is essential in various biomaterial applications. In this study, we have used a multidisciplinary approach that combines biological and physicochemical methods to progress in our understanding of cell-surface interactions. Four model surfaces have been used to investigate fibronectin (Fn) adsorption and the subsequent morphology and adhesion of preosteoblasts. Such experimental conditions lead us to distinguish between anti- and proadhesive substrata. Our results indicate that Fn is not able to induce cell adhesion on antiadhesive materials. On adhesive substrata, Fn did not increase the number of adherent cells but favored their spreading. This work also examined Fn-surface interactions using ELISA immunoassays, fluorescent labeling of Fn, and force spectroscopy with Fn-modified tips. The results provided clear evidence of the advantages and limitations of each technique. All of the techniques confirmed the important adsorption of Fn on proadhesive surfaces for cells. By contrast, antiadhesive substrata for cells avoided Fn adsorption. Furthermore, ELISA experiments enabled us to verify the accessibility of cell binding sites to adsorbed Fn molecules.
在各种生物材料应用中,开发具有粘附性和抗粘附性的表面至关重要。在本研究中,我们采用了多学科方法,将生物学和物理化学方法相结合,以增进我们对细胞-表面相互作用的理解。我们使用了四种模型表面来研究纤连蛋白(Fn)的吸附以及成骨前体细胞随后的形态和粘附情况。这样的实验条件使我们能够区分抗粘附和促粘附基质。我们的结果表明,Fn无法在抗粘附材料上诱导细胞粘附。在粘附基质上,Fn并没有增加粘附细胞的数量,但有利于细胞铺展。这项工作还使用酶联免疫吸附测定(ELISA)、Fn的荧光标记以及用Fn修饰的探针进行力谱分析来研究Fn与表面的相互作用。结果清楚地证明了每种技术的优缺点。所有技术都证实了Fn在细胞促粘附表面上的重要吸附。相比之下,细胞抗粘附基质可避免Fn吸附。此外,ELISA实验使我们能够验证细胞结合位点对吸附的Fn分子的可及性。