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A quantitative high-resolution computational mechanics cell model for growing and regenerating tissues

机译:一种用于生长和再生组织的定量高分辨率计算力学细胞模型

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Mathematical models are increasingly designed to guide experiments in biology, biotechnology, as well as to assist in medical decision making. They are in particular important to understand emergent collective cell behavior. For this purpose, the models, despite still abstractions of reality, need to be quantitative in all aspects relevant for the question of interest. This paper considers as showcase example the regeneration of liver after drug-induced depletion of hepatocytes, in which the surviving and dividing hepatocytes must squeeze in between the blood vessels of a network to refill the emerged lesions. Here, the cells' response to mechanical stress might significantly impact the regeneration process. We present a 3D high-resolution cell-based model integrating information from measurements in order to obtain a refined and quantitative understanding of the impact of cell-biomechanical effects on the closure of drug-induced lesions in liver. Our model represents each cell individually and is constructed by a discrete, physically scalable network of viscoelastic elements, capable of mimicking realistic cell deformation and supplying information at subcellular scales. The cells have the capability to migrate, grow, and divide, and the nature and parameters of their mechanical elements can be inferred from comparisons with optical stretcher experiments. Due to triangulation of the cell surface, interactions of cells with arbitrarily shaped (triangulated) structures such as blood vessels can be captured naturally. Comparing our simulations with those of so-called center-based models, in which cells have a largely rigid shape and forces are exerted between cell centers, we find that the migration forces a cell needs to exert on its environment to close a tissue lesion, is much smaller than predicted by center-based models. To stress generality of the approach, the liver simulations were complemented by monolayer and multicellular spheroid growth simulations. In summary, our model can give quantitative insight in many tissue organization processes, permits hypothesis testing in silico, and guide experiments in situations in which cell mechanics is considered important.
机译:数学模型越来越旨在指导生物学,生物技术的实验,以及协助医学决策。他们特别重要,以了解紧急集体细胞行为。为此目的,模型尽管仍然存在现实,但需要在对兴趣问题相关的所有方面进行定量。本文认为展示肝脏诱导肝细胞耗尽后肝脏再生,其中存活和分裂肝细胞必须在网络的血管之间挤压以重新填充出现的病变。这里,细胞对机械应力的反应可能会显着影响再生过程。我们介绍了一种基于3D高分辨率小区的模型,其集成了来自测量的信息,以获得对细胞 - 生物力学效应对肝脏诱导药物诱导病变的影响的精细和定量理解。我们的模型单独代表每个单元,并且由粘弹性元件的离散,物理可伸缩的网络构成,能够模仿现实的细胞变形和在亚细胞尺度处提供信息。细胞具有迁移,生长和分割的能力,并且可以从光学担架实验的比较中推断出其机械元件的性质和参数。由于细胞表面的三角测量,可以自然地捕获具有任意形状(三角形)结构的细胞与诸如血管的相互作用。将模拟与所谓的基于中心的模型进行比较,其中细胞在细胞中心施加电池具有很大的刚性形状和力,我们发现迁移力需要施加细胞以缩短组织病变,以缩短组织病变,远小于基于中心的模型预测。为了强调这种方法,肝脏模拟被单层和多细胞球体生长模拟互补。总之,我们的模型可以在许多组织组织过程中提供定量洞察力,允许在硅中的假设检测,并指导实验在细胞力学被认为是重要的情况下。

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