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The Influence of Plastic Deformation Mechanisms on the Adhesion Behavior and Collagen Formation in Osteoblast Cells

机译:塑性变形机制对成骨细胞黏附行为和胶原形成的影响

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In many of biomedical applications, the implant might get in direct contact with the bone tissue where the osteogenesis needs to be stimulated. If osteoblasts can not successfully attach on the implant surface, the bone might resorb and implant can fail. In the current study MC3T3 cells were cultured on the 316L stainless steel samples which were deformed up to four different strain levels (5, 15, 25 and 35%) to activate plastic deformation mechanisms (slip and twinning) in different volume fractions. Scanning electron microscopy (SEM) images showed that cells adhered and spread significantly on the 25 and 35% deformed samples owing to the greater surface roughness and energy provided by the increased density of micro-deformation mechanisms which promoted the formation of focal contacts. In addition, significant amount of collagen formation was observed on the sample deformed up to 25% of strain which can be due to the ideal match of the surface roughness and collagen molecules. Overall these results show that material's microstructure can be manipulated through plastic deformation mechanisms in order to enhance the cell response and collagen deposition. As a result long lasting implants could be obtained which would eliminate additional surgical interventions and provide a successful treatment.
机译:在许多生物医学应用中,植入物可能与需要刺激成骨作用的骨组织直接接触。如果成骨细胞不能成功地附着在植入物表面,则骨头可能会吸收并导致植入物失败。在当前的研究中,将MC3T3细胞培养在316L不锈钢样品上,将其变形至四个不同的应变水平(5、15、25和35%),以激活不同体积分数的塑性变形机制(滑动和孪生)。扫描电子显微镜(SEM)图像显示,由于表面粗糙度增加和微形变机制密度增加而提供了更大的能量,从而促进了焦点接触的形成,因此细胞在25%和35%变形的样品上显着粘附并扩散。此外,在样品变形高达25%的样品上观察到大量胶原蛋白形成,这可能是由于表面粗糙度和胶原蛋白分子的理想匹配所致。总体而言,这些结果表明,可以通过塑性变形机制来控制材料的微观结构,从而增强细胞反应和胶原蛋白的沉积。结果,可以获得持久的植入物,这将消除额外的外科手术干预并提供成功的治疗。

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