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Vertex dynamics simulations of viscosity-dependent deformation during tissue morphogenesis

机译:组织形态发生过程中粘度依赖性变形的顶点动力学模拟

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In biological development, multiple cells cooperate to form tissue morphologies based on their mechanical interactions; namely active force generation and passive viscoelastic response. In particular, the dynamic processes of tissue deformations are governed by the viscous properties of the tissues. These properties are spatially inhomogeneous because they depend on the tissue constituents, such as cytoplasm, cytoskeleton, basement membrane and extracellular matrix. The multicellular mechanics of tissue morphogenesis have been investigated in vertex dynamics models. However, conventional models are applicable only to quasi-static deformation processes, which do not account for tissue viscosities. We propose a vertex dynamics model that simulates the viscosity-dependent dynamic deformation processes during tissue morphogenesis. By incorporating local velocity fields into the governing equation of vertex movements, the model turns Galilean invariant. In addition, the viscous properties of tissue components are newly expressed by formulating friction forces on vertices as functions of the relative velocities among the vertices. The advantages of the proposed model are examined by epithelial growth simulations under the employed condition for quasi-static processes. As a result, the epithelial vesicle simulated by the proposed model is linearly elongated with nearly free stress, while that simulated by the conventional model is undulated with compressive residual stress. Therefore, the proposed model is able to reflect the timescale of deformations by satisfying Galilean invariance. Next, the applicability of the proposed model is assessed in epithelial growth simulations of viscous extracellular materials. In this test, the epithelial vesicles are deformed into tubular shapes by oriented cell divisions, and their morphologies are extremely sensitive to extracellular viscosity. Therefore, the dynamic deformations in the proposed model depend on the viscous properties of tissue components. The proposed model will be useful for simulating dynamic deformation processes of tissue morphogenesis depending on viscous properties of various tissue components.
机译:在生物发育中,多个细胞根据其机械相互作用共同形成组织形态。即主动力产生和被动粘弹性响应。特别地,组织变形的动态过程受组织的粘性特性支配。这些特性在空间上是不均匀的,因为它们取决于组织成分,例如细胞质,细胞骨架,基底膜和细胞外基质。在顶点动力学模型中已经研究了组织形态发生的多细胞力学。但是,常规模型仅适用于准静态变形过程,该过程不考虑组织粘度。我们提出了一个顶点动力学模型,可以模拟组织形态发生过程中与粘度有关的动态变形过程。通过将局部速度场合并到顶点运动的控制方程中,该模型使Galilean不变。另外,通过将顶点上的摩擦力表示为顶点之间的相对速度的函数,来新表达组织成分的粘性。在准静态过程的采用条件下,通过上皮生长模拟检验了所提出模型的优势。结果,所提出的模型模拟的上皮囊泡在几乎没有自由应力的情况下线性伸长,而常规模型所模拟的上皮囊泡在压缩残余应力下起伏。因此,提出的模型能够通过满足伽利略不变性来反映变形的时间尺度。接下来,在粘性细胞外材料的上皮生长模拟中评估了所提出模型的适用性。在该测试中,上皮囊泡通过定向的细胞分裂而变形为管状,并且它们的形态对细胞外粘度极为敏感。因此,提出的模型中的动态变形取决于组织成分的粘性。所提出的模型将可用于模拟组织形态发生的动态变形过程,具体取决于各种组织成分的粘性。

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