A density-independent rigidity transition in biological tissues

被引:3
|
作者
Bi, Dapeng [1 ]
Lopez, J. H. [1 ]
Schwarz, J. M. [1 ,2 ]
Manning, M. Lisa [1 ,2 ]
机构
[1] Syracuse Univ, Dept Phys, Syracuse, NY 13244 USA
[2] Syracuse Biomat Inst, Syracuse, NY 13244 USA
基金
美国国家科学基金会;
关键词
CORTICAL TENSION; CELL; MECHANICS; ADHESION; MIGRATION; DYNAMICS; DRIVEN;
D O I
10.1038/NPHYS3471
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Cell migration is important in many biological processes, including embryonic development, cancer metastasis and wound healing. In these tissues, a cell's motion is often strongly constrained by its neighbours, leading to glassy dynamics. Although self-propelled particle models exhibit a density-driven glass transition, this does not explain liquid-to-solid transitions in confluent tissues, where there are no gaps between cells and therefore the density is constant. Here we demonstrate the existence of a new type of rigidity transition that occurs in the well-studied vertex model for confluent tissue monolayers at constant density. We find that the onset of rigidity is governed by a model parameter that encodes single-cell properties such as cell-cell adhesion and cortical tension, providing an explanation for liquid-to-solid transitions in confluent tissues and making testable predictions about how these transitions differ from those in particulate matter.
引用
收藏
页码:1074 / +
页数:7
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