Zhao Jieling, Naveed Hammad, Kachalo Sema, Cao Youfang, Tian Wei, Liang Jie
Annu Int Conf IEEE Eng Med Biol Soc. 2013;2013:4517-20. doi: 10.1109/EMBC.2013.6610551.
Understanding the geometric, topologic, and mechanical properties of cells and their interactions is critical for studying tissue pattern formation and organ development. Computational model and tools for simulating cell pattern formation have broad implications in studying embryogenesis, blood-vessel development, tissue regeneration, and tumor growth. Although a number of cell modeling methods exist, they do not simultaneously account for detailed cellular shapes as well as dynamic changes in cell geometry and topology. Here we describe a dynamic finite element cell model (dFEMC) for studying populations of cells and tissue development. By incorporating details of cell shape, cell growth and shrinkage, cell birth and death, cell division and fusion, our method can model realistically a variety problems of cell pattern formation. We give two examples of applying our method to the study of cell fusion and cell apoptosis. The dFEMC model developed here provides a general computational framework for studying dynamics pattern formation of tissue.
了解细胞的几何、拓扑和力学特性及其相互作用对于研究组织模式形成和器官发育至关重要。用于模拟细胞模式形成的计算模型和工具在研究胚胎发生、血管发育、组织再生和肿瘤生长方面具有广泛的意义。尽管存在许多细胞建模方法,但它们不能同时考虑细胞的详细形状以及细胞几何和拓扑的动态变化。在这里,我们描述了一种用于研究细胞群体和组织发育的动态有限元细胞模型(dFEMC)。通过纳入细胞形状、细胞生长和收缩、细胞出生和死亡、细胞分裂和融合的细节,我们的方法可以逼真地模拟各种细胞模式形成问题。我们给出了两个将我们的方法应用于细胞融合和细胞凋亡研究的例子。这里开发的dFEMC模型为研究组织的动态模式形成提供了一个通用的计算框架。