Formation of motile cell clusters in heterogeneous model tumors: The role of cell-cell alignment.

IF 2.4 3区 物理与天体物理 Q2 PHYSICS, FLUIDS & PLASMAS Physical Review E Pub Date : 2024-12-01 DOI:10.1103/PhysRevE.110.064401
Quirine J S Braat, Cornelis Storm, Liesbeth M C Janssen
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Abstract

Circulating tumor cell clusters play an important role in the metastatic cascade. These clusters can acquire a migratory and more invasive phenotype, and coordinate their motion to migrate as a collective. Before such clusters can form by collectively detaching from a primary tumor, however, the cluster must first aggregate in the tumor interior. The mechanism of this cluster formation process is still poorly understood. One of the possible ways for cells to cluster is by aligning their direction of motion with their neighboring cells. This work aims to investigate the role of this cell-cell alignment interaction on the formation of motile cell clusters inside the bulk of a tumor using computer simulations. We employ a cellular Potts model in which we model a two-dimensional heterogeneous confluent layer containing both motile and nonmotile cells. Our results indicate that the degree of clustering is governed by two distinct processes: the formation of clusters due to the presence of cell-cell alignment interactions among motile cells, and the suppression of clustering due to the presence of the dynamic cellular environment (comprising the nonmotile cells). We find that the largest motile clusters are formed for intermediate alignment strengths, contrary to what is observed for motile cells in free space (that is, unimpeded by a dense cellular environment), in which case stronger cell-cell alignment always leads to larger clustering. Our findings suggest that the presence of a densely packed cellular environment and strong cell-cell alignment inhibits the formation of large migratory clusters within the primary tumor, providing physical insight into potential factors at play during the early stages of metastasis.

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异质性肿瘤模型中运动细胞簇的形成:细胞-细胞排列的作用。
循环肿瘤细胞簇在转移级联中起重要作用。这些集群可以获得迁移和更具侵袭性的表型,并协调它们作为一个集体迁移的运动。然而,在通过集体脱离原发肿瘤形成这种簇之前,簇必须首先聚集在肿瘤内部。这种星团形成过程的机制仍然知之甚少。细胞聚集的一种可能方法是使它们的运动方向与邻近细胞对齐。这项工作的目的是利用计算机模拟研究这种细胞-细胞排列相互作用对肿瘤内部运动细胞簇形成的作用。我们采用了一个细胞波茨模型,在这个模型中,我们模拟了一个包含运动细胞和非运动细胞的二维异质融合层。我们的研究结果表明,聚类的程度由两个不同的过程控制:由于运动细胞之间存在细胞-细胞排列相互作用而形成的聚类,以及由于动态细胞环境(包括非运动细胞)的存在而抑制聚类。我们发现,最大的运动细胞簇是在中间排列强度下形成的,这与在自由空间(即不受密集细胞环境阻碍)中观察到的运动细胞相反,在这种情况下,更强的细胞-细胞排列总是导致更大的集群。我们的研究结果表明,密集的细胞环境和强大的细胞-细胞排列抑制了原发肿瘤内大迁移簇的形成,为转移早期阶段的潜在因素提供了物理见解。
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来源期刊
Physical Review E
Physical Review E PHYSICS, FLUIDS & PLASMASPHYSICS, MATHEMAT-PHYSICS, MATHEMATICAL
CiteScore
4.50
自引率
16.70%
发文量
2110
期刊介绍: Physical Review E (PRE), broad and interdisciplinary in scope, focuses on collective phenomena of many-body systems, with statistical physics and nonlinear dynamics as the central themes of the journal. Physical Review E publishes recent developments in biological and soft matter physics including granular materials, colloids, complex fluids, liquid crystals, and polymers. The journal covers fluid dynamics and plasma physics and includes sections on computational and interdisciplinary physics, for example, complex networks.
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