Active wetting of epithelial tissues: modeling considerations

IF 2.2 4区 生物学 Q3 BIOPHYSICS
Ivana Pajic-Lijakovic, Milan Milivojevic
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引用次数: 4

Abstract

Morphogenesis, tissue regeneration, and cancer invasion involve transitions in tissue morphology. These transitions, caused by collective cell migration (CCM), have been interpreted as active wetting/de-wetting transitions. This phenomenon is considered based on a model system as wetting of a cell aggregate on a rigid substrate, which includes cell aggregate movement and isotropic/anisotropic spreading of a cell monolayer around the aggregate depending on the substrate rigidity and aggregate size. This model system accounts for the transition between 3D epithelial aggregate and 2D cell monolayer as a product of: (1) tissue surface tension, (2) surface tension of substrate matrix, (3) cell–matrix interfacial tension, (4) interfacial tension gradient, (5) viscoelasticity caused by CCM, and (6) viscoelasticity of substrate matrix. These physical parameters depend on the cell contractility and state of cell–cell and cell–matrix adhesion contacts, as well as the stretching/compression of cellular systems caused by CCM. Despite extensive research devoted to study cell wetting, we still do not understand the interplay among these physical parameters which induces an oscillatory trend of cell rearrangement. This review focuses on these physical parameters in governing the cell rearrangement in the context of epithelial aggregate wetting/de-wetting, and on modeling approaches aimed at reproducing and understanding these biological systems. In this context, we not only review previously published biophysical models for cell rearrangement caused by CCM, but also propose new extensions of those models to point out the interrelation between cell–matrix interfacial tension and epithelial viscoelasticity and the role of the interfacial tension gradient in cell spreading.

主动润湿上皮组织:建模考虑
形态发生、组织再生和肿瘤侵袭涉及组织形态的转变。这些转变是由集体细胞迁移(CCM)引起的,被解释为主动润湿/去润湿转变。这种现象被认为是基于一个模型系统,即细胞聚集体在刚性衬底上的润湿,其中包括细胞聚集体的运动和细胞单层在聚集体周围的各向同性/各向异性扩散,这取决于衬底刚度和聚集体尺寸。该模型系统解释了从3D上皮聚集体到2D细胞单层的转变是以下因素的产物:(1)组织表面张力,(2)基质表面张力,(3)细胞-基质界面张力,(4)界面张力梯度,(5)CCM引起的粘弹性,(6)基质粘弹性。这些物理参数取决于细胞的收缩性和细胞-细胞和细胞-基质粘附接触的状态,以及由CCM引起的细胞系统的拉伸/压缩。尽管对细胞润湿进行了广泛的研究,但我们仍然不了解这些物理参数之间的相互作用,这些参数导致细胞重排的振荡趋势。这篇综述的重点是在上皮聚集体润湿/去润湿的背景下控制细胞重排的这些物理参数,以及旨在再现和理解这些生物系统的建模方法。在此背景下,我们不仅回顾了先前发表的CCM引起的细胞重排的生物物理模型,而且还提出了这些模型的新扩展,以指出细胞-基质界面张力和上皮粘弹性之间的相互关系以及界面张力梯度在细胞扩散中的作用。
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来源期刊
European Biophysics Journal
European Biophysics Journal 生物-生物物理
CiteScore
4.30
自引率
0.00%
发文量
43
审稿时长
6-12 weeks
期刊介绍: The journal publishes papers in the field of biophysics, which is defined as the study of biological phenomena by using physical methods and concepts. Original papers, reviews and Biophysics letters are published. The primary goal of this journal is to advance the understanding of biological structure and function by application of the principles of physical science, and by presenting the work in a biophysical context. Papers employing a distinctively biophysical approach at all levels of biological organisation will be considered, as will both experimental and theoretical studies. The criteria for acceptance are scientific content, originality and relevance to biological systems of current interest and importance. Principal areas of interest include: - Structure and dynamics of biological macromolecules - Membrane biophysics and ion channels - Cell biophysics and organisation - Macromolecular assemblies - Biophysical methods and instrumentation - Advanced microscopics - System dynamics.
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