Active Vertex Model for cell-resolution description of epithelial tissue mechanics

被引:188
作者
Barton, Daniel L. [1 ,2 ]
Henkes, Silke [3 ]
Weijer, Cornelis J. [4 ]
Sknepnek, Rastko [1 ,2 ]
机构
[1] Univ Dundee, Sch Sci & Engn, Div Phys, Dundee, Scotland
[2] Univ Dundee, Sch Life Sci, Div Computat Biol, Dundee, Scotland
[3] Univ Aberdeen, Dept Phys, Inst Complex Syst & Math Biol, Aberdeen, Scotland
[4] Univ Dundee, Sch Life Sci, Div Cell & Dev Biol, Dundee, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
COLLECTIVE MIGRATION; CONTACT INHIBITION; INTESTINAL CRYPT; SHAPE CHANGES; FORCES; DYNAMICS; ADHESION; MORPHOGENESIS; REARRANGEMENT; PROLIFERATION;
D O I
10.1371/journal.pcbi.1005569
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We introduce an Active Vertex Model (AVM) for cell-resolution studies of the mechanics of confluent epithelial tissues consisting of tens of thousands of cells, with a level of detail inaccessible to similar methods. The AVM combines the Vertex Model for confluent epithelial tissues with active matter dynamics. This introduces a natural description of the cell motion and accounts for motion patterns observed on multiple scales. Furthermore, cell contacts are generated dynamically from positions of cell centres. This not only enables efficient numerical implementation, but provides a natural description of the T1 transition events responsible for local tissue rearrangements. The AVM also includes cell alignment, cell-specific mechanical properties, cell growth, division and apoptosis. In addition, the AVM introduces a flexible, dynamically changing boundary of the epithelial sheet allowing for studies of phenomena such as the fingering instability or wound healing. We illustrate these capabilities with a number of case studies.
引用
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页数:34
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