An Open-source Python Tool for Traction Force Microscopy on Micropatterned Substrates.

IF 1 Q3 BIOLOGY
Artur Ruppel, Vladimir Misiak, Martial Balland
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引用次数: 0

Abstract

Cell-generated forces play a critical role in driving and regulating complex biological processes, such as cell migration and division and cell and tissue morphogenesis in development and disease. Traction force microscopy (TFM) is an established technique developed in the field of mechanobiology used to quantify cellular forces exerted on soft substrates and internal mechanical tissue stresses. TFM measures cell-generated traction forces in 2D or 3D environments with varying mechanical and biochemical properties. This technique involves embedding fiducial markers in the substrate, imaging substrate deformations caused by the cells, and using mathematical models to infer forces. This protocol compiles procedures from various previously published studies and software packages and describes how to perform TFM on 2D micropatterned substrates. Although not the focus of this protocol, the methods and software packages shown here also allow to perform monolayer stress microscopy (MSM), a method to calculate internal mechanical stress within the cells by modeling them as a thin plate with linear and homogeneous material properties. TFM and MSM are non-invasive methods capable of yielding spatially and temporally resolved force and stress maps with high throughput. As such, they enable the generation of rich datasets, which can provide valuable insights into the roles of cell-generated forces in various physiological and pathological processes. Key features • TFM and MSM protocol for 2D micropatterned polyacrylamide substrates, from sample preparation over imaging to data analysis with provided code. • Sample preparation method is based on Tseng et al. [1]. • TFM analysis is done with Python custom code and is optimized for batch analysis of movies. • MSM analysis is done with pyTFM from Bauer et al. [2].

用于微图案化基板上牵引力显微镜的开源Python工具。
细胞产生的力量在驱动和调节复杂的生物过程中起着关键作用,例如细胞迁移和分裂以及发育和疾病中的细胞和组织形态发生。牵引力显微镜(TFM)是机械生物学领域发展起来的一项成熟技术,用于量化施加在软基质上的细胞力和内部机械组织应力。TFM测量细胞在2D或3D环境中产生的牵引力,具有不同的机械和生化特性。该技术包括在衬底中嵌入基准标记,成像由细胞引起的衬底变形,并使用数学模型来推断力。本协议汇编了各种先前发表的研究和软件包的程序,并描述了如何在2D微图案基板上执行TFM。虽然不是本协议的重点,但这里展示的方法和软件包也允许执行单层应力显微镜(MSM),一种通过将细胞建模为具有线性和均匀材料特性的薄板来计算细胞内部机械应力的方法。TFM和MSM是一种非侵入性方法,能够产生高通量的空间和时间分辨力和应力图。因此,它们能够生成丰富的数据集,这可以为细胞产生的力在各种生理和病理过程中的作用提供有价值的见解。主要特点•二维微图案聚丙烯酰胺衬底的TFM和MSM协议,从样品制备到成像到提供代码的数据分析。•样品制备方法基于Tseng et al.[1]。•TFM分析使用Python自定义代码完成,并针对电影的批量分析进行了优化。•MSM分析是用Bauer等人的pyTFM完成的。
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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来源期刊
CiteScore
1.50
自引率
0.00%
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