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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Cell shape and spreading of stromal (mesenchymal) stem cells cultured on fibronectin coated gold and hydroxyapatite surfaces
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Cell shape and spreading of stromal (mesenchymal) stem cells cultured on fibronectin coated gold and hydroxyapatite surfaces

机译:在纤连蛋白包被的金和羟基磷灰石表面上培养的基质(间质)干细胞的细胞形状和扩散

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In order to identify the cellular mechanisms leading to the biocompatibility of hydroxyapatite implants, we studied the interaction of human bone marrow derived stromal (mesenchymal) stem cells (hMSCs) with fibronectin-coated gold (Au) and hydroxyapatite (HA) surfaces. The adsorption of fibronectin was monitored by Quartz Crystal Microbalance with Dissipation (QCM-D) at two different concentrations, 20μg/ml and 200μg/ml, and the fibronectin adsorption experiments were complemented with antibody measurements. The QCM-D results show that the surface mass uptake is largest on the Au surfaces, while the number of polyclonal and monoclonal antibodies directed against the cell-binding domain (CB-domain) on the fibronectin (Fn) is significantly larger on the (HA) surfaces. Moreover, a higher number of antibodies bound to the fibronectin coatings formed from the highest bulk fibronection concentration. In subsequent cell studies with hMSC's we studied the cell spreading, cytoskeletal organization and cell morphology on the respective surfaces. When the cells were adsorbed on the uncoated substrates, a diffuse cell actin cytoskeleton was revealed, and the cells had a highly elongated shape. On the fibronectin coated surfaces the cells adapted to a more polygonal shape with a well-defined actin cytoskeleton, while a larger cell area and roundness values were observed for cells cultured on the coated surfaces. Among the coated surfaces a slightly larger cell area and roundness values was observed on HA as compared to Au. Moreover, the results revealed that the morphology of cells cultured on fibronectin coated HA surfaces were less irregular. In summary we find that fibronectin adsorbs in a more activated state on the HA surfaces, resulting in a slightly different cellular response as compared to the fibronectin coated Au surfaces.
机译:为了确定导致羟基磷灰石植入物生物相容性的细胞机制,我们研究了人骨髓来源的基质(间质)干细胞(hMSCs)与纤连蛋白包被的金(Au)和羟基磷灰石(HA)表面的相互作用。通过耗散的石英晶体微天平(QCM-D)监测纤连蛋白的吸附,两种浓度分别为20μg/ ml和200μg/ ml,并结合抗体测量来补充纤连蛋白的吸附实验。 QCM-D结果表明,在Au表面上表面吸收最大,而在纤连蛋白(Fn)上针对细胞结合结构域(CB-domain)的多克隆抗体和单克隆抗体的数量则明显多于( HA)表面。而且,更多的抗体与纤连蛋白涂层结合是由最高的总纤化浓度形成的。在随后的使用hMSC进行的细胞研究中,我们研究了各自表面上的细胞扩散,细胞骨架组织和细胞形态。当细胞吸附在未涂覆的基质上时,显示出弥漫性细胞肌动蛋白细胞骨架,并且细胞具有高度伸长的形状。在纤连蛋白包被的表面上,细胞适应了更明确的肌动蛋白细胞骨架的多边形形状,而在包被的表面上培养的细胞则观察到更大的细胞面积和圆度值。在涂层表面中,与金相比,在HA上观察到了稍大的泡孔面积和圆度值。此外,结果表明在纤连蛋白包被的HA表面上培养的细胞的形态不规则。总而言之,我们发现纤连蛋白以更活化的状态吸附在HA表面上,与纤连蛋白包被的Au表面相比,导致细胞反应略有不同。

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