Olenka Jain, Brato Chakrabarti, Reza Farhadifar, Elizabeth R. Gavis, Michael J. Shelley, Stanislav Y. Shvartsman
{"title":"大规模细胞内流动的几何效应","authors":"Olenka Jain, Brato Chakrabarti, Reza Farhadifar, Elizabeth R. Gavis, Michael J. Shelley, Stanislav Y. Shvartsman","doi":"arxiv-2409.06763","DOIUrl":null,"url":null,"abstract":"This work probes the role of cell geometry in orienting self-organized fluid\nflows in the late stage Drosophila oocyte. Recent theoretical work has shown\nthat a model, which relies only on hydrodynamic interactions of flexible,\ncortically anchored microtubules (MTs) and the mechanical loads from molecular\nmotors moving upon them, is sufficient to generate observed flows. While the\nemergence of flows has been studied in spheres, oocytes change shape during\nstreaming and it was unclear how robust these flows are to the geometry of the\ncell. Here we use biophysical theory and computational analysis to investigate\nthe role of geometry and find that the axis of rotation is set by the shape of\nthe domain and that the flow is robust to biologically relevant perturbations\nof the domain shape. Using live imaging and 3D flow reconstruction, we test the\npredictions of the theory/simulation, finding consistency between the model and\nlive experiments, further demonstrating a geometric dependence on flow\ndirection in late-stage Drosophila oocytes.","PeriodicalId":501321,"journal":{"name":"arXiv - QuanBio - Cell Behavior","volume":"148 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Geometric Effects in Large Scale Intracellular Flows\",\"authors\":\"Olenka Jain, Brato Chakrabarti, Reza Farhadifar, Elizabeth R. Gavis, Michael J. Shelley, Stanislav Y. Shvartsman\",\"doi\":\"arxiv-2409.06763\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This work probes the role of cell geometry in orienting self-organized fluid\\nflows in the late stage Drosophila oocyte. Recent theoretical work has shown\\nthat a model, which relies only on hydrodynamic interactions of flexible,\\ncortically anchored microtubules (MTs) and the mechanical loads from molecular\\nmotors moving upon them, is sufficient to generate observed flows. While the\\nemergence of flows has been studied in spheres, oocytes change shape during\\nstreaming and it was unclear how robust these flows are to the geometry of the\\ncell. Here we use biophysical theory and computational analysis to investigate\\nthe role of geometry and find that the axis of rotation is set by the shape of\\nthe domain and that the flow is robust to biologically relevant perturbations\\nof the domain shape. Using live imaging and 3D flow reconstruction, we test the\\npredictions of the theory/simulation, finding consistency between the model and\\nlive experiments, further demonstrating a geometric dependence on flow\\ndirection in late-stage Drosophila oocytes.\",\"PeriodicalId\":501321,\"journal\":{\"name\":\"arXiv - QuanBio - Cell Behavior\",\"volume\":\"148 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-10\",\"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-2409.06763\",\"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-2409.06763","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Geometric Effects in Large Scale Intracellular Flows
This work probes the role of cell geometry in orienting self-organized fluid
flows in the late stage Drosophila oocyte. Recent theoretical work has shown
that a model, which relies only on hydrodynamic interactions of flexible,
cortically anchored microtubules (MTs) and the mechanical loads from molecular
motors moving upon them, is sufficient to generate observed flows. While the
emergence of flows has been studied in spheres, oocytes change shape during
streaming and it was unclear how robust these flows are to the geometry of the
cell. Here we use biophysical theory and computational analysis to investigate
the role of geometry and find that the axis of rotation is set by the shape of
the domain and that the flow is robust to biologically relevant perturbations
of the domain shape. Using live imaging and 3D flow reconstruction, we test the
predictions of the theory/simulation, finding consistency between the model and
live experiments, further demonstrating a geometric dependence on flow
direction in late-stage Drosophila oocytes.