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Biomineralization of a self-assembled extracellular matrix for bone tissue engineering.

机译:骨组织工程自组装细胞外基质的生物丙原化。

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Understanding how biomineralization occurs in the extracellular matrix (ECM) of bone cells is crucial to the understanding of bone formation and the development of a successfully engineered bone tissue scaffold. It is still unclear how ECM mechanical properties affect protein-mineral interactions in early stages of bone mineralization. We investigated the longitudinal mineralization properties of MC3T3-E1 cells and the elastic modulus of their ECM using shear modulation force microscopy, synchrotron grazing incidence X-ray diffraction (GIXD), scanning electron microscopy, energy dispersive X-ray spectroscopy, and confocal laser scanning microscopy (CLSM). The elastic modulus of the ECM fibers underwent significant changes for the mineralizing cells, which were not observed in the nonmineralizing cells. On substrates conducive to ECM network production, the elastic modulus of mineralizing cells increased at time points corresponding to mineral production, whereas that of the nonmineralizing cells did not vary over time. The presence of hydroxyapatite in mineralizing cells and the absence thereof in the nonmineralizing ones were confirmed by GIXD, and CLSM showed that a restructuring of actin occurred only for mineral-producing cells. These results show that the correct and complete development of the ECM network is required for osteoblasts to mineralize. This in turn requires a suitably prepared synthetic substrate for bone development to succeed in vitro.
机译:了解生物矿化在骨细胞的细胞外基质(ECM)中是如何对骨骼形成的理解至关重要,以及成功设计的骨组织支架的发展。尚不清楚ECM机械性能如何影响骨矿化早期蛋白质 - 矿物质相互作用。我们研究了MC3T3-E1细胞的纵向矿化性能和其ECM的弹性模量使用剪切调制力显微镜,同步辐射入射X射线衍射(GIXD),扫描电子显微镜,能量分散X射线光谱和共聚焦激光扫描显微镜(CLSM)。 ECM纤维的弹性模量接受了在非丙烯化细胞中未观察到的矿化细胞的显着变化。在有利于ECM网络生产的基材上,矿化细胞的弹性模量在对应于矿产生产的时间点增加,而非丙烯化细胞的弹性模量随时间没有变化。通过GixD确认矿化细胞中羟基磷灰石的存在和非丙烯化合物中的不存在,CLSM表明,CLSM仅针对矿物生产细胞发生的肌动蛋白的重组。这些结果表明,ECM网络的正确和完全开发是对矿化的骨质细胞所必需的。这反过来需要适当制备的合成衬底,用于骨骼发育以体外成功。

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