Shubhadeep Sadhukhan, Cristina Martinez-Torres, Samo Penič, Carsten Beta, Aleš Iglič, Nir S Gov
{"title":"模拟叶状薄片驱动的细胞如何保持持续迁移并与外部障碍相互作用","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":"{\"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}","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}
Modelling how lamellipodia-driven cells maintain persistent migration and interact with external barriers
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.