首页> 外文期刊>Regenerative Biomaterials >Adsorption of plasma proteins and fibronectin on poly(hydroxylethyl methacrylate) brushes of different thickness and their relationship with adhesion and migration of vascular smooth muscle cells
【24h】

Adsorption of plasma proteins and fibronectin on poly(hydroxylethyl methacrylate) brushes of different thickness and their relationship with adhesion and migration of vascular smooth muscle cells

机译:血浆蛋白和纤连蛋白在不同厚度的聚甲基丙烯酸羟乙酯刷上的吸附及其与血管平滑肌细胞黏附和迁移的关系

获取原文
       

摘要

The surface-grafted poly(hydroxylethyl methacrylate) (PHEMA) molecules were demonstrated to show a brush state regardless of their molecular length (molecular weight). Adsorption of proteins from 10% fetal bovine serum (FBS), fibronectin (Fn) and bovine serum albumin (BSA) was quantified by ellipsometry, revealing that the amounts of FBS and Fn decreased monotonously along with the increase of PHEMA thickness, whereas not detectable for BSA when the PHEMA thickness was larger than 6 nm. Radio immunoassay found that the adsorption of Fn from 10% FBS had no significant difference regardless of the PHEMA thickness. However, ELISA results showed that the Arg-Gly-Asp (RGD) activity of adsorbed Fn decreased with the increase of PHEMA thickness. By comparison of cellular behaviors of vascular smooth muscle cells (VSMCs) being cultured in vitro in the normal serum-containing medium and the Fn-depleted serum-containing medium, the significant role of Fn on modulating the adhesion and migration of VSMCs was verified. Taking account all the results, the Fn adsorption model and its role on linking the biomaterials surface to the VSMCs behaviors are proposed.
机译:已证明表面接枝的聚(甲基丙烯酸羟乙酯)(PHEMA)分子无论其分子长度(分子量)如何均显示刷状。椭圆光度法定量分析了10%胎牛血清(FBS),纤连蛋白(Fn)和牛血清白蛋白(BSA)对蛋白质的吸附,结果表明,随着PHEMA厚度的增加,FBS和Fn的含量单调减少,但无法检测到当PHEMA厚度大于6 nm时,对于BSA而言。放射免疫分析发现,无论PHEMA厚度如何,从10%FBS吸附Fn都没有显着差异。但是,ELISA结果表明,随着PHEMA厚度的增加,吸附的Fn的Arg-Gly-Asp(RGD)活性降低。通过比较在正常含血清培养基和贫Fn含血清培养基中体外培养的血管平滑肌细胞(VSMC)的细胞行为,证实了Fn在调节VSMC粘附和迁移中的重要作用。考虑到所有结果,提出了Fn吸附模型及其在将生物材料表面连接到VSMCs行为上的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号