{"title":"Origin of yield stress and mechanical plasticity in biological tissues","authors":"Anh Q. Nguyen, Junxiang Huang, Dapeng Bi","doi":"arxiv-2409.04383","DOIUrl":null,"url":null,"abstract":"During development and under normal physiological conditions, biological\ntissues are continuously subjected to substantial mechanical stresses. In\nresponse to large deformations cells in a tissue must undergo multicellular\nrearrangements in order to maintain integrity and robustness. However, how\nthese events are connected in time and space remains unknown. Here, using\ncomputational and theoretical modeling, we studied the mechanical plasticity of\nepithelial monolayers under large deformations. Our results demonstrate that\nthe jamming-unjamming (solid-fluid) transition in tissues can vary\nsignificantly depending on the degree of deformation, implying that tissues are\nhighly unconventional materials. Using analytical modeling, we elucidate the\norigins of this behavior. We also demonstrate how a tissue accommodates large\ndeformations through a collective series of rearrangements, which behave\nsimilarly to avalanches in non-living materials. We find that these tissue\navalanches are governed by stress redistribution and the spatial distribution\nof vulnerable spots. Finally, we propose a simple and experimentally accessible\nframework to predict avalanches and infer tissue mechanical stress based on\nstatic images.","PeriodicalId":501040,"journal":{"name":"arXiv - PHYS - Biological Physics","volume":"20 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - PHYS - Biological Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.04383","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
During development and under normal physiological conditions, biological
tissues are continuously subjected to substantial mechanical stresses. In
response to large deformations cells in a tissue must undergo multicellular
rearrangements in order to maintain integrity and robustness. However, how
these events are connected in time and space remains unknown. Here, using
computational and theoretical modeling, we studied the mechanical plasticity of
epithelial monolayers under large deformations. Our results demonstrate that
the jamming-unjamming (solid-fluid) transition in tissues can vary
significantly depending on the degree of deformation, implying that tissues are
highly unconventional materials. Using analytical modeling, we elucidate the
origins of this behavior. We also demonstrate how a tissue accommodates large
deformations through a collective series of rearrangements, which behave
similarly to avalanches in non-living materials. We find that these tissue
avalanches are governed by stress redistribution and the spatial distribution
of vulnerable spots. Finally, we propose a simple and experimentally accessible
framework to predict avalanches and infer tissue mechanical stress based on
static images.