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首页> 外文期刊>Journal of the mechanical behavior of biomedical materials >Affine and non-affine deformations quantified in cytoskeletal networks through three-dimensional form-finding model
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Affine and non-affine deformations quantified in cytoskeletal networks through three-dimensional form-finding model

机译:通过三维形式发现模型在细胞骨骼网络中定量仿射和非仿射变形

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摘要

Actin filaments and cross-linkers are main components of cytoskeletal networks in eukaryotic cells, and they support bending moments and axial forces respectively. A three-dimensional form-finding model is proposed in this work to investigate affine and non-affine deformations in cytoskeletal networks. In recent studies, modeling of cytoskeletal networks turns out to be a key piece in the cell mechanics puzzle. We used form-finding analysis to compute and analyze cytoskeletal models. A three-dimensional model is much more flexible and contains more elements than a two-dimensional model, and non-linear finite element analysis is difficult to converge. Thus, vector form intrinsic finite element analysis is employed here for valid results. The three-dimensional model reveals new behaviors beyond earlier two-dimensional models and better aligns with available data. Relative density of actin filaments and height of the form-finding model both play important roles in determining cytoskeletal stiffness, positively and negatively, respectively. Real cytoskeletal networks are quite mixed in terms of affine and non-affine deformations, which are quantified by internal strain energy in actin filaments and cross linkers. Results are also influenced by actin filament relative density and height of the model. The three-dimensional form-fording model does provide much more room for intensive studies on cytoskeletal networks. In our future study, micro tubules, fluidics, viscoelastic-plastic cross-linkers and even the whole cell model may be taken into account gradually to improve the cytoskeletal form-finding model.
机译:肌动蛋白细丝和交联剂是真核细胞中细胞骨骼网络的主要成分,并且它们分别支持弯曲的时刻和轴力。在这项工作中提出了一种三维形式发现模型,以研究细胞骨架网络中的仿射和非仿射变形。在最近的研究中,细胞骨骼网络的建模在细胞力学拼图中成为一个关键件。我们使用表单发现分析来计算和分析细胞骨骼模型。三维模型更灵活,并且包含比二维模型更多的元素,并且难以收敛非线性有限元分析。因此,载体形成内在有限元分析用于有效结果。三维模型揭示了早期二维模型之外的新行为,并更好地与可用数据对齐。肌动蛋白细丝的相对密度和形式发现模型的高度分别在测定细胞骨架刚度,积极和负面的情况下起重要作用。真正的细胞骨骼网络在仿射和非仿射变形方面非常混合,其通过肌动蛋白长丝和交叉连接器中的内部应变能量量化。结果也受到模型的肌动蛋白丝相对密度和高度的影响。三维形式的模型为细胞骨骼网络提供了更多的重症研究空间。在我们未来的研究中,可以逐渐考虑微管,流体,粘弹性塑料交联剂及甚至整个细胞模型,以改善细胞骨骼形成模型。

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