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亚细胞尺度下弯曲细胞-细胞界面的二维顶点模型。

A two-dimensional vertex model for curvy cell-cell interfaces at the subcellular scale.

机构信息

Department of Physics, Syracuse University , Syracuse, NY 13244, USA.

Indian Creek Farm , Ithaca, NY 14850, USA.

出版信息

J R Soc Interface. 2024 Aug;21(217):20240193. doi: 10.1098/rsif.2024.0193. Epub 2024 Aug 28.

DOI:10.1098/rsif.2024.0193
PMID:39192725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11407580/
Abstract

Cross-sections of cell shapes in a tissue monolayer typically resemble a tiling of convex polygons. Yet, examples exist where the polygons are not convex with curved cell-cell interfaces, as seen in the adaxial epidermis. To date, two-dimensional vertex models predicting the structure and mechanics of cell monolayers have been mostly limited to convex polygons. To overcome this limitation, we introduce a framework to study curvy cell-cell interfaces at the subcellular scale within vertex models by using a parametrized curve between vertices that is expanded in a Fourier series and whose coefficients represent additional degrees of freedom. This extension to non-convex polygons allows for cells with the same shape index, or dimensionless perimeter, to be, for example, either elongated or globular with lobes. In the presence of applied, anisotropic stresses, we find that local, subcellular curvature or buckling can be energetically more favourable than larger scale deformations involving groups of cells. Inspired by recent experiments, we also find that local, subcellular curvature at cell-cell interfaces emerges in a group of cells in response to the swelling of additional cells surrounding the group. Our framework, therefore, can account for a wider array of multicellular responses to constraints in the tissue environment.

摘要

组织单层中细胞形状的横截面通常类似于凸多边形的平铺。然而,存在一些多边形不是凸的,细胞-细胞界面是弯曲的,如在近轴表皮中所见。迄今为止,预测细胞单层结构和力学的二维顶点模型主要局限于凸多边形。为了克服这一限制,我们引入了一个框架,通过在顶点之间使用参数化曲线来研究子细胞尺度上的弯曲细胞-细胞界面,该曲线在傅里叶级数中展开,其系数表示额外的自由度。这种对非凸多边形的扩展允许具有相同形状指数(或无维周长)的细胞,例如,要么是拉长的,要么是带有叶的球状。在施加各向异性应力的情况下,我们发现局部、子细胞曲率或屈曲可能比涉及多个细胞的更大尺度变形更具能量优势。受最近实验的启发,我们还发现,在一组细胞中,细胞-细胞界面的局部、子细胞曲率在一组细胞周围的额外细胞肿胀时出现。因此,我们的框架可以解释更广泛的细胞对组织环境约束的反应。