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Main Authors: Zhang, Jiusi, Chan, Chung Wing, Li, Bo, Zhang, Rui
Format: Preprint
Published: 2025
Subjects:
Online Access:https://arxiv.org/abs/2506.04068
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author Zhang, Jiusi
Chan, Chung Wing
Li, Bo
Zhang, Rui
author_facet Zhang, Jiusi
Chan, Chung Wing
Li, Bo
Zhang, Rui
contents Collective cell migration governs a range of physiological and pathological processes, from tissue morphogenesis to cancer invasion, in which topological defects arise as an inevitable consequence of frequent cellular rearrangement and migration. Here, we employ an Active Vertex Model to investigate structural defects generated in the wake of transported cells. We find that while the drag coefficient of a cell in a perfect lattice is anisotropic, the threshold drag force required to mobilize the cell is isotropic. Remarkably, we find that dragging two neighboring cells along the direction of least-resistance minimizes lattice disruption. By comparing defect-healing behaviors across different physical models, we disentangle the contributions of cell adhesion and many-body interactions. Together, our findings provide new insights into the topological organization of confluent tissues during collective migration, advancing our physical understanding of cellular transport processes such as wound healing, tissue repair, and cancer metastasis.
format Preprint
id arxiv_https___arxiv_org_abs_2506_04068
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Topological Defects Mediate Collective Transport of Confluent Cells
Zhang, Jiusi
Chan, Chung Wing
Li, Bo
Zhang, Rui
Soft Condensed Matter
Collective cell migration governs a range of physiological and pathological processes, from tissue morphogenesis to cancer invasion, in which topological defects arise as an inevitable consequence of frequent cellular rearrangement and migration. Here, we employ an Active Vertex Model to investigate structural defects generated in the wake of transported cells. We find that while the drag coefficient of a cell in a perfect lattice is anisotropic, the threshold drag force required to mobilize the cell is isotropic. Remarkably, we find that dragging two neighboring cells along the direction of least-resistance minimizes lattice disruption. By comparing defect-healing behaviors across different physical models, we disentangle the contributions of cell adhesion and many-body interactions. Together, our findings provide new insights into the topological organization of confluent tissues during collective migration, advancing our physical understanding of cellular transport processes such as wound healing, tissue repair, and cancer metastasis.
title Topological Defects Mediate Collective Transport of Confluent Cells
topic Soft Condensed Matter
url https://arxiv.org/abs/2506.04068