Pajic-Lijakovic Ivana, Milivojevic Milan
Faculty of Technology and Metallurgy, Department of Chemical Engineering, University of Belgrade, Karnegijeva 4, 11000, Belgrade, Serbia.
Eur Biophys J. 2023 Feb;52(1-2):1-15. doi: 10.1007/s00249-022-01625-w. Epub 2023 Jan 2.
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.
形态发生、组织再生和癌症侵袭都涉及组织形态的转变。这些由集体细胞迁移(CCM)引起的转变被解释为主动浸润/去浸润转变。这种现象是基于一个模型系统来考虑的,即细胞聚集体在刚性基质上的浸润,其中包括细胞聚集体的移动以及细胞单层围绕聚集体的各向同性/各向异性扩散,这取决于基质的刚性和聚集体的大小。这个模型系统将三维上皮聚集体和二维细胞单层之间的转变解释为以下因素的产物:(1)组织表面张力,(2)基质的表面张力,(3)细胞 - 基质界面张力,(4)界面张力梯度,(5)CCM引起的粘弹性,以及(6)基质的粘弹性。这些物理参数取决于细胞的收缩性、细胞 - 细胞和细胞 - 基质粘附接触的状态,以及CCM引起的细胞系统的拉伸/压缩。尽管对细胞浸润的研究广泛,但我们仍然不了解这些物理参数之间的相互作用,正是这种相互作用引发了细胞重排的振荡趋势。本综述聚焦于上皮聚集体浸润/去浸润背景下控制细胞重排的这些物理参数,以及旨在重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关于CCM引起的细胞重排的生物物理模型,还提出了这些模型的新扩展,以指出细胞 - 基质界面张力与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。