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Competitive protein adsorption on micro patterned polymeric biomaterials, and viscoelastic properties of tailor made extracellular matrices.

机译:竞争性蛋白质在微图案化聚合物生物材料上的吸附以及量身定制的细胞外基质的粘弹性质。

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Cell adhesion on biomaterial surfaces and the vitality of anchorage dependent cells is affected by several parameters of an adsorbate layer which is intentionally or spontaneously formed. Surface pre-treatments and several conditioning steps prior and during to the cell/biomaterial contact affect the composition, orientation, quantity and viscoelasticity of the interfacing layer between cells and biomaterial. This work was performed to elucidate the response of cells on two modified biomaterial surfaces based on protein or carbohydrate adsorbates: (a) Masked UV irradiations opened a simple route to obtain chemically patterned substrates controlling serum protein adsorption and cell adhesion. It is possible to achieve structures of subcellular size and to produce immobilized gradients. In order to examine the protein matrix deposited on these substrates we applied a quartz microbalance technique (QCM-D) capable to extract viscoelastic data in addition to the mass uptake during plasma protein deposition.It was found that the quantity and viscosity of surface bound albumin is lowered when the surface is modified (patterned) by UV exposure. Hence, the UV modification promotes the competitive adsorption of cell adhesion proteins from the media or upon secretion by the cells and yields to the observed cell patterns. (b) Another tissue engineering technique, using immobilized, modified and/or cross linked hyaluronic acid (HA), an important extra cellular matrix component in vivo, is also examined by QCM-D. Our data demonstrate that HA can be modified by an activation with a carbodiimide, followed by the application of an alpha,omega-bisamino polyethyleneglycol. The QCM-D data can be interpreted as a stiffening of the HA layer combined with the release of hydration water. Further, the hydration state and the viscoelastic behaviour of surface bound ultrathin HA hydrogels was examined. Quantification of viscoelastic parameters of thin films of ECM by QCM-D is valuable for the interpretation of durotaxis, describing effects of mechanical substrate parameters on the adhesion and motility of cells.
机译:生物材料表面上的细胞粘附和锚定依赖性细胞的活力受有意或自发形成的吸附层的几个参数影响。细胞/生物材料接触之前和期间的表面预处理和几个调节步骤会影响细胞与生物材料之间的界面层的组成,取向,数量和粘弹性。进行这项工作是为了阐明细胞在两个基于蛋白质或碳水化合物吸附物的改性生物材料表面上的反应:(a)遮罩的紫外线辐射开辟了一条简单的途径,即可获得化学图案化的底物,以控制血清蛋白的吸附和细胞粘附。可以实现亚细胞大小的结构并产生固定的梯度。为了检查沉积在这些基质上的蛋白质基质,我们使用了石英微天平技术(QCM-D),该技术除了可以提取血浆蛋白质沉积过程中的质量摄取外,还可以提取粘弹性数据。发现表面结合白蛋白的数量和粘度当通过紫外线暴露对表面进行修饰(构图)时,表面粗糙度降低。因此,紫外线修饰促进了细胞粘附蛋白从培养基中或细胞分泌后的竞争性吸附,并产生了观察到的细胞模式。 (b)QCM-D还研究了另一种组织工程技术,该技术使用固定的,修饰的和/或交联的透明质酸(HA),这是体内重要的细胞外基质成分。我们的数据表明,可以通过用碳二亚胺活化,然后再应用α,ω-双氨基氨基聚乙二醇来修饰HA。 QCM-D数据可以解释为HA层变硬并释放出水合水。此外,检查了表面结合的超薄HA水凝胶的水合状态和粘弹性行为。通过QCM-D量化ECM薄膜的粘弹性参数对于解释durotaxis具有重要意义,它描述了机械基质参数对细胞粘附和运动的影响。

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