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Experimental characterization and computational modelling of two-dimensional cell spreading for skeletal regeneration

机译:二维细胞扩展用于骨骼再生的实验表征和计算模型

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摘要

Limited cell ingrowth is a major problem for tissue engineering and the clinical application of porous biomaterials as bone substitutes. As a first step, migration and proliferation of an interacting cell population can be studied in two-dimensional culture. Mathematical modelling is essential to generalize the results of these experiments and to derive the intrinsic parameters that can be used for predictions. However, a more thorough evaluation of theoretical models is hampered by limited experimental observations. In this study, experiments and image analysis methods were developed to provide a detailed spatial and temporal picture of how cell distributions evolve. These methods were used to quantify the migration and proliferation of skeletal cell types including MG63 and human bone marrow stromal cells (HBMSCs). The high level of detail with which the cell distributions were mapped enabled a precise assessment of the correspondence between experimental results and theoretical model predictions. This analysis revealed that the standard Fisher equation is appropriate for describing the migration behaviour of the HBMSC population, while for the MG63 cells a sharp front model is more appropriate. In combination with experiments, this type of mathematical model will prove useful in predicting cell ingrowth and improving strategies and control of skeletal tissue regeneration.
机译:对于组织工程和多孔生物材料作为骨替代物的临床应用而言,有限的细胞向内生长是一个主要问题。第一步,可以在二维培养中研究相互作用细胞群的迁移和增殖。数学建模对于概括这些实验的结果以及导出可用于预测的内在参数至关重要。但是,有限的实验观察结果阻碍了对理论模型的更全面评估。在这项研究中,开发了实验和图像分析方法,以提供细胞分布如何演变的详细时空图。这些方法用于量化骨骼细胞类型(包括MG63和人类骨髓基质细胞(HBMSC))的迁移和增殖。细胞分布图的高细节水平使得能够精确评估实验结果与理论模型预测之间的对应关系。该分析表明,标准的Fisher方程适合描述HBMSC群体的迁移行为,而对于MG63细胞而言,锋利的前沿模型更为合适。结合实验,这种类型的数学模型将对预测细胞向内生长以及改善骨骼组织再生的策略和控制很有用。

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