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用于骨骼再生的二维细胞铺展的实验表征与计算建模

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

作者信息

Sengers Bram G, Please Colin P, Oreffo Richard O C

机构信息

Bone and Joint Research Group, Developmental Origins of Health and Disease, University of Southampton, Southampton General Hospital, Southampton, UK.

出版信息

J R Soc Interface. 2007 Dec 22;4(17):1107-17. doi: 10.1098/rsif.2007.0233.

Abstract

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.

摘要

有限的细胞向内生长是组织工程以及多孔生物材料作为骨替代物临床应用中的一个主要问题。第一步,可以在二维培养中研究相互作用的细胞群体的迁移和增殖。数学建模对于归纳这些实验结果并推导可用于预测的内在参数至关重要。然而,理论模型更全面的评估受到有限实验观察结果的阻碍。在本研究中,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景。这些方法用于量化包括MG63和人骨髓基质细胞(HBMSC)在内的骨骼细胞类型的迁移和增殖。绘制细胞分布的高度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Fisher方程适用于描述HBMSC群体的迁移行为,而对于MG63细胞,尖锐前沿模型更合适。结合实验,这种类型的数学模型将被证明在预测细胞向内生长以及改进骨骼组织再生的策略和控制方面是有用的。

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