Burmeister J S, McKinney V Z, Reichert W M, Truskey G A
Department of Biomedical Engineering, Duke University, Box 90281, Durham, North Carolina 27708-0281, USA.
J Biomed Mater Res. 1999 Dec 15;47(4):577-84. doi: 10.1002/(sici)1097-4636(19991215)47:4<577::aid-jbm15>3.0.co;2-s.
The objective of this study was to examine the effect of substrate hydrophobicity on cell-substrate contact area and the affinity between adsorbed fibronectin (Fn) and its receptor. Homo- and copolymer films of hydrophobic ethyl methacrylate (EMA) and hydrophilic hydroxyethyl methacrylate (HEMA) were spun-cast onto glass slides. Bovine aortic endothelial cells (BAEC) were plated for 2 h in serum-free medium onto polymers preadsorbed with Fn. Cells were fixed, labeled, and examined by total internal reflection fluorescence microscopy (TIRFM) to determine the topography of the basal surface as a function of distance from the substrate. Phase contrast microscopy was used to examine the total projected area of adherent cells. The cumulative contact area was greatest on cells attached to surfaces prepared from 0% HEMA and lowest on surfaces with the highest HEMA content. An equilibrium adhesion model used these data together with the critical force for detachment and the Fn density (Burmeister et al., J Biomed Mater Res 1996;30:13-22) to determine the affinity between Fn and its receptor and the bond strength. The affinity and force per bond decreased with increasing HEMA content. These results indicate that differences in the strength of endothelial cell adhesion to polymers are influenced by the conformation of the adsorbed adhesion proteins.
本研究的目的是考察底物疏水性对细胞-底物接触面积以及吸附的纤连蛋白(Fn)与其受体之间亲和力的影响。将疏水性甲基丙烯酸乙酯(EMA)和亲水性甲基丙烯酸羟乙酯(HEMA)的均聚物和共聚物薄膜旋涂到载玻片上。将牛主动脉内皮细胞(BAEC)在无血清培养基中接种到预先吸附有Fn的聚合物上2小时。通过全内反射荧光显微镜(TIRFM)对细胞进行固定、标记和检查,以确定基底表面形貌与距底物距离的函数关系。利用相差显微镜检查贴壁细胞的总投影面积。累积接触面积在附着于由0% HEMA制备的表面的细胞上最大,而在HEMA含量最高的表面上最小。一个平衡粘附模型将这些数据与脱离临界力和Fn密度(Burmeister等人,《生物医学材料研究杂志》1996年;30:13 - 22)结合起来,以确定Fn与其受体之间的亲和力和键强度。随着HEMA含量的增加,亲和力和每个键的力降低。这些结果表明,内皮细胞与聚合物粘附强度的差异受吸附的粘附蛋白构象的影响。