Shubhadeep Sadhukhan, Cristina Martinez-Torres, Samo Penič, Carsten Beta, Aleš Iglič, Nir S Gov
{"title":"Modelling how lamellipodia-driven cells maintain persistent migration and interact with external barriers","authors":"Shubhadeep Sadhukhan, Cristina Martinez-Torres, Samo Penič, Carsten Beta, Aleš Iglič, Nir S Gov","doi":"arxiv-2409.04772","DOIUrl":null,"url":null,"abstract":"Cell motility is fundamental to many biological processes, and cells exhibit\na variety of migration patterns. Many motile cell types follow a universal law\nthat connects their speed and persistency, a property that can originate from\nthe intracellular transport of polarity cues due to the global actin retrograde\nflow. This mechanism was termed the ``Universal Coupling between cell Speed and\nPersistency\"(UCSP). Here we implemented a simplified version of the UCSP\nmechanism in a coarse-grained ``minimal-cell\" model, which is composed of a\nthree-dimensional vesicle that contains curved active proteins. This model\nspontaneously forms a lamellipodia-like motile cell shape, which is however\nsensitive and can depolarize into a non-motile form due to random fluctuations\nor when interacting with external obstacles. The UCSP implementation introduces\nlong-range inhibition, which stabilizes the motile phenotype. This allows our\nmodel to describe the robust polarity observed in cells and explain a large\nvariety of cellular dynamics, such as the relation between cell speed and\naspect ratio, cell-barrier scattering, and cellular oscillations in different\ntypes of geometric confinements.","PeriodicalId":501321,"journal":{"name":"arXiv - QuanBio - Cell Behavior","volume":"116 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Cell Behavior","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.04772","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
Cell motility is fundamental to many biological processes, and cells exhibit
a variety of migration patterns. Many motile cell types follow a universal law
that connects their speed and persistency, a property that can originate from
the intracellular transport of polarity cues due to the global actin retrograde
flow. This mechanism was termed the ``Universal Coupling between cell Speed and
Persistency"(UCSP). Here we implemented a simplified version of the UCSP
mechanism in a coarse-grained ``minimal-cell" model, which is composed of a
three-dimensional vesicle that contains curved active proteins. This model
spontaneously forms a lamellipodia-like motile cell shape, which is however
sensitive and can depolarize into a non-motile form due to random fluctuations
or when interacting with external obstacles. The UCSP implementation introduces
long-range inhibition, which stabilizes the motile phenotype. This allows our
model to describe the robust polarity observed in cells and explain a large
variety of cellular dynamics, such as the relation between cell speed and
aspect ratio, cell-barrier scattering, and cellular oscillations in different
types of geometric confinements.