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Potential of electrospun cationic BSA fibers to guide osteogenic MSC differentiation via surface charge and fibrous topography

机译:电纺器阳离子BSA纤维的潜力,以通过表面电荷和纤维形貌引导成骨MSC分化

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Large or complex bone fractures often need clinical treatments for sufficient bone repair. New treatment strategies have pursued the idea of using mesenchymal stromal cells (MSCs) in combination with osteoinductive materials to guide differentiation of MSCs into bone cells ensuring complete bone regeneration. To overcome the challenge of developing such materials, fundamental studies are needed to analyze and understand the MSC behavior on modified surfaces of applicable materials for bone healing. For this purpose, we developed a fibrous scaffold resembling the bone/bone marrow extracellular matrix (ECM) based on protein without addition of synthetic polymers. With this biomimetic in vitro model we identified the fibrous structure as well as the charge of the material to be responsible for its effects on?MSC differentiation. Positive charge was introduced via cationization that additionally supported the stability of the scaffold in cell culture, and acted as nucleation point for mineralization during osteogenesis. Furthermore, we revealed enhanced focal adhesion formation and osteogenic differentiation of MSCs cultured on positively charged protein fibers. This pure protein-based and chemically modifiable, fibrous ECM model allows the investigation of MSC behavior on biomimetic materials to unfold new vistas how to direct cells' differentiation for the development of new bone regenerating strategies.
机译:大或复杂的骨折通常需要临床治疗方法足够的骨修复。新的治疗策略追求使用间充质基质细胞(MSCs)与骨诱导材料组合使用,以将MSCs的分化导入骨细胞,确保完全骨再生。为了克服开发这种材料的挑战,需要基本研究来分析和理解适用材料的改进表面的MSC行为,用于骨愈合。为此目的,我们开发了一种类似于骨髓/骨髓细胞外基质(ECM)的纤维支架,而不加入合成聚合物。通过这种仿生体外模型,我们鉴定了纤维结构以及材料对其对其作用的影响的纤维化结构。通过阳离子化引入阳性电荷,该阳离子化另外支持细胞培养中支架的稳定性,并在骨质发生过程中用作矿化的成核点。此外,我们揭示了在带正电荷的蛋白纤维上培养的MSCs的增强的局部粘附形成和成骨分化。这种基于纯蛋白质和化学可改性的纤维ECM模型可以调查仿生材料的MSC行为,展开新的Vistas如何指导细胞的分化为新的骨再生策略的发展。

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