Simulating Organogenesis in COMSOL: Comparison Of Methods For Simulating Branching Morphogenesis

L. D. Wittwer, M. Peters, S. Aland, D. Iber
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引用次数: 2

Abstract

During organogenesis tissue grows and deforms. The growth processes are controlled by diffusible proteins, so-called morphogens. Many different patterning mechanisms have been proposed. The stereotypic branching program during lung development can be recapitulated by a receptor-ligand based Turing model. Our group has previously used the Arbitrary Lagrangian-Eulerian (ALE) framework for solving the receptor-ligand Turing model on growing lung domains. However, complex mesh deformations which occur during lung growth severely limit the number of branch generations that can be simulated. A new Phase-Field implementation avoids mesh deformations by considering the surface of the modelling domains as interfaces between phases, and by coupling the reaction-diffusion framework to these surfaces. In this paper, we present a rigorous comparison between the Phase-Field approach and the ALE-based simulation.
在COMSOL中模拟器官发生:模拟分支形态发生方法的比较
在器官发生过程中,组织生长和变形。生长过程是由可扩散的蛋白质控制的,即所谓的形态形成因子。已经提出了许多不同的模式机制。肺发育过程中的刻板分支程序可以通过基于受体配体的图灵模型来概括。我们的团队以前使用任意拉格朗日-欧拉(ALE)框架来解决生长肺域的受体-配体图灵模型。然而,在肺生长过程中发生的复杂网格变形严重限制了可以模拟的分支世代的数量。一种新的相场实现通过将建模域的表面视为相之间的界面,并通过将反应扩散框架耦合到这些表面来避免网格变形。在本文中,我们对相场方法和基于ale的仿真进行了严格的比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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