Lukas RiedelHeidelberg University, Valentin WössnerHeidelberg University, Dominic KempfHeidelberg University, Falko ZiebertHeidelberg University, Peter BastianHeidelberg University, Ulrich S. SchwarzHeidelberg University
{"title":"收缩细胞中应力纤维的定位可最大限度地减少内部机械应力","authors":"Lukas RiedelHeidelberg University, Valentin WössnerHeidelberg University, Dominic KempfHeidelberg University, Falko ZiebertHeidelberg University, Peter BastianHeidelberg University, Ulrich S. SchwarzHeidelberg University","doi":"arxiv-2407.07797","DOIUrl":null,"url":null,"abstract":"The mechanics of animal cells is strongly determined by stress fibers, which\nare contractile filament bundles that form dynamically in response to\nextracellular cues. Stress fibers allow the cell to adapt its mechanics to\nenvironmental conditions and to protect it from structural damage. While the\nphysical description of single stress fibers is well-developed, much less is\nknown about their spatial distribution on the level of whole cells. Here, we\ncombine a finite element method for one-dimensional fibers embedded in an\nelastic bulk medium with dynamical rules for stress fiber formation based on\ngenetic algorithms. We postulate that their main goal is to achieve minimal\nmechanical stress in the bulk material with as few fibers as possible. The\nfiber positions and configurations resulting from this optimization task alone\nare in good agreement with those found in experiments where cells in\n3D-scaffolds were mechanically strained at one attachment point. For optimized\nconfigurations, we find that stress fibers typically run through the cell in a\ndiagonal fashion, similar to reinforcement strategies used for composite\nmaterial.","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"25 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The positioning of stress fibers in contractile cells minimizes internal mechanical stress\",\"authors\":\"Lukas RiedelHeidelberg University, Valentin WössnerHeidelberg University, Dominic KempfHeidelberg University, Falko ZiebertHeidelberg University, Peter BastianHeidelberg University, Ulrich S. SchwarzHeidelberg University\",\"doi\":\"arxiv-2407.07797\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The mechanics of animal cells is strongly determined by stress fibers, which\\nare contractile filament bundles that form dynamically in response to\\nextracellular cues. Stress fibers allow the cell to adapt its mechanics to\\nenvironmental conditions and to protect it from structural damage. While the\\nphysical description of single stress fibers is well-developed, much less is\\nknown about their spatial distribution on the level of whole cells. Here, we\\ncombine a finite element method for one-dimensional fibers embedded in an\\nelastic bulk medium with dynamical rules for stress fiber formation based on\\ngenetic algorithms. We postulate that their main goal is to achieve minimal\\nmechanical stress in the bulk material with as few fibers as possible. The\\nfiber positions and configurations resulting from this optimization task alone\\nare in good agreement with those found in experiments where cells in\\n3D-scaffolds were mechanically strained at one attachment point. For optimized\\nconfigurations, we find that stress fibers typically run through the cell in a\\ndiagonal fashion, similar to reinforcement strategies used for composite\\nmaterial.\",\"PeriodicalId\":501170,\"journal\":{\"name\":\"arXiv - QuanBio - Subcellular Processes\",\"volume\":\"25 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - QuanBio - Subcellular Processes\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2407.07797\",\"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 - Subcellular Processes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2407.07797","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The positioning of stress fibers in contractile cells minimizes internal mechanical stress
The mechanics of animal cells is strongly determined by stress fibers, which
are contractile filament bundles that form dynamically in response to
extracellular cues. Stress fibers allow the cell to adapt its mechanics to
environmental conditions and to protect it from structural damage. While the
physical description of single stress fibers is well-developed, much less is
known about their spatial distribution on the level of whole cells. Here, we
combine a finite element method for one-dimensional fibers embedded in an
elastic bulk medium with dynamical rules for stress fiber formation based on
genetic algorithms. We postulate that their main goal is to achieve minimal
mechanical stress in the bulk material with as few fibers as possible. The
fiber positions and configurations resulting from this optimization task alone
are in good agreement with those found in experiments where cells in
3D-scaffolds were mechanically strained at one attachment point. For optimized
configurations, we find that stress fibers typically run through the cell in a
diagonal fashion, similar to reinforcement strategies used for composite
material.