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arXiv 2005.12678q-bio.CBq-bio.QM
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用规则化轮廓流分析变形虫细胞运动中的突起动力学

Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows

Daniel Schindler, Ted Moldenhawer, Maike Stange, Valentino Lepro, Carsten Beta, Matthias Holschneider, Wilhelm Huisinga

摘要:

阿米巴样细胞的运动性是必不可少的广泛的生物过程,包括伤口愈合,胚胎形态发生,和癌症转移。它依赖于细胞形状变化的复杂动态模式,这对数学建模构成了长期的挑战,并提出了对自动化和可重复方法的需求,以从图像序列中提取定量形态学特征。在这里,我们介绍了一个理论框架和计算方法,从堆栈的分割显微镜图像的时空轮廓动态获得平滑表示。基于高斯过程回归,我们提出了一个单参数家庭的正则化轮廓流,使我们能够连续跟踪连续的细胞轮廓之间的参考点(虚拟标记)。我们使用这种方法来定义一个坐标系上的移动细胞的边界,并表示在这个参考系中的不同的局部几何量。特别是,我们引入了局部标记分散作为一种措施,以确定局部膜扩张,并提供了一个完全自动化的方式来提取这种扩张的属性,包括它们的面积和生长时间。这些方法可以作为一个名为AmoePy的开源软件包使用,这是一个基于Python的工具箱,用于分析变形虫细胞运动性(基于延时显微镜数据),包括图形用户界面和详细的文档。由于我们的框架的数学严谨性,我们设想它是用于开发新的细胞运动模型。我们主要使用实验数据的社会阿米巴Dictyosteelicdiscoideum来说明和验证我们的方法。

英文摘要:

Amoeboid cell motility is essential for a wide range of biological processes including wound healing, embryonic morphogenesis, and cancer metastasis. It relies on complex dynamical patterns of cell shape changes that pose long-standing challenges to mathematical modeling and raise a need for automated and reproducible approaches to extract quantitative morphological features from image sequences. Here, we introduce a theoretical framework and a computational method for obtaining smooth representations of the spatiotemporal contour dynamics from stacks of segmented microscopy images. Based on a Gaussian process regression we propose a one-parameter family of regularized contour flows that allows us to continuously track reference points (virtual markers) between successive cell contours. We use this approach to define a coordinate system on the moving cell boundary and to represent different local geometric quantities in this frame of reference. In particular, we introduce the local marker dispersion as a measure to identify localized membrane expansions and provide a fully automated way to extract the properties of such expansions, including their area and growth time. The methods are available as an open-source software package called AmoePy, a Python-based toolbox for analyzing amoeboid cell motility (based on time-lapse microscopy data), including a graphical user interface and detailed documentation. Due to the mathematical rigor of our framework, we envision it to be of use for the development of novel cell motility models. We mainly use experimental data of the social amoeba Dictyostelium discoideum to illustrate and validate our approach.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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