平面弹性基底上细胞的机械感应和机械诱导集体运动的数学模型

IF 3 3区 医学 Q2 BIOPHYSICS
Riham K. Ahmed, Tamer Abdalrahman, Neil H. Davies, Fred Vermolen, Thomas Franz
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引用次数: 0

摘要

细胞机械地与环境相互作用,以感知地形、弹性和来自其他细胞的机械信号。机械传感对细胞行为有深远的影响,包括运动。目前的研究旨在建立平面弹性基质上细胞机械传感的数学模型,并证明该模型对群体中单个细胞运动的预测能力。在该模型中,假设细胞传递由动态焦点粘附整合素密度产生的粘附力,该粘附力局部变形基底,并感知来自邻近细胞的基底变形。多个单元的基底变形表示为具有空间变化梯度的总应变能密度。细胞位置梯度的大小和方向决定了细胞的运动。细胞-底物摩擦,部分运动随机性,细胞死亡和分裂都包括在内。在不同的衬底弹性和厚度下,给出了衬底的单胞变形和双胞运动。25个细胞在均匀底物上的集体运动性模拟了200µm圆形伤口的闭合,预测了确定性和随机运动。研究了4个细胞和15个细胞在不同弹性和厚度的基质上的细胞运动,后者再次模拟伤口愈合。伤口闭合用45个细胞来演示迁移过程中细胞死亡和分裂的模拟。该数学模型能较好地模拟平面弹性基底上机械诱导的集体细胞运动。该模型适用于扩展到其他细胞和底物形状,并包含趋化线索,为体外和体内研究提供了补充的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mathematical model of mechano-sensing and mechanically induced collective motility of cells on planar elastic substrates

Cells mechanically interact with their environment to sense, for example, topography, elasticity and mechanical cues from other cells. Mechano-sensing has profound effects on cellular behaviour, including motility. The current study aims to develop a mathematical model of cellular mechano-sensing on planar elastic substrates and demonstrate the model’s predictive capabilities for the motility of individual cells in a colony. In the model, a cell is assumed to transmit an adhesion force, derived from a dynamic focal adhesion integrin density, that locally deforms a substrate, and to sense substrate deformation originating from neighbouring cells. The substrate deformation from multiple cells is expressed as total strain energy density with a spatially varying gradient. The magnitude and direction of the gradient at the cell location define the cell motion. Cell–substrate friction, partial motion randomness, and cell death and division are included. The substrate deformation by a single cell and the motility of two cells are presented for several substrate elasticities and thicknesses. The collective motility of 25 cells on a uniform substrate mimicking the closure of a circular wound of 200 µm is predicted for deterministic and random motion. Cell motility on substrates with varying elasticity and thickness is explored for four cells and 15 cells, the latter again mimicking wound closure. Wound closure by 45 cells is used to demonstrate the simulation of cell death and division during migration. The mathematical model can adequately simulate the mechanically induced collective cell motility on planar elastic substrates. The model is suitable for extension to other cell and substrates shapes and the inclusion of chemotactic cues, offering the potential to complement in vitro and in vivo studies.

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来源期刊
Biomechanics and Modeling in Mechanobiology
Biomechanics and Modeling in Mechanobiology 工程技术-工程:生物医学
CiteScore
7.10
自引率
8.60%
发文量
119
审稿时长
6 months
期刊介绍: Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that (1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury, (2) identify and quantify mechanosensitive responses and their mechanisms, (3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and (4) report discoveries that advance therapeutic and diagnostic procedures. Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.
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