Actin dynamics sustains spatial gradients of membrane tension in adherent cells

bioRxiv Pub Date : 2024-07-16 DOI:10.1101/2024.07.15.603517
J. M. García-Arcos, Amine Mehidi, Julissa Sánchez Velázquez, Pau Guillamat, C. Tomba, Laura Houzet, L. Capolupo, Giovanni D’Angelo, Adai Colom, Elizabeth Hinde, Charlotte Aumeier, Aurélien Roux
{"title":"Actin dynamics sustains spatial gradients of membrane tension in adherent cells","authors":"J. M. García-Arcos, Amine Mehidi, Julissa Sánchez Velázquez, Pau Guillamat, C. Tomba, Laura Houzet, L. Capolupo, Giovanni D’Angelo, Adai Colom, Elizabeth Hinde, Charlotte Aumeier, Aurélien Roux","doi":"10.1101/2024.07.15.603517","DOIUrl":null,"url":null,"abstract":"Tension propagates extremely fast in lipid bilayers, precluding the formation of tension gradients. Nevertheless, plasma membrane tension gradients have been evidenced in migrating cells and along axons. Here, using a fluorescent membrane tension probe, we show that membrane tension gradients exist in all adherent cells, whether they migrate or not. Non-adhering cells do not display tension gradients. We further show that branched actin increases tension, while membrane-to-cortex attachments facilitate its propagation. Tension is the lowest at the edge of adhesion sites and highest at protrusions, setting the boundaries of the tension gradients. By providing a quantitative and mechanistic basis behind the organization of membrane tension gradients, our work explains how they are actively sustained in adherent cells.","PeriodicalId":9124,"journal":{"name":"bioRxiv","volume":"60 18","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.07.15.603517","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

Tension propagates extremely fast in lipid bilayers, precluding the formation of tension gradients. Nevertheless, plasma membrane tension gradients have been evidenced in migrating cells and along axons. Here, using a fluorescent membrane tension probe, we show that membrane tension gradients exist in all adherent cells, whether they migrate or not. Non-adhering cells do not display tension gradients. We further show that branched actin increases tension, while membrane-to-cortex attachments facilitate its propagation. Tension is the lowest at the edge of adhesion sites and highest at protrusions, setting the boundaries of the tension gradients. By providing a quantitative and mechanistic basis behind the organization of membrane tension gradients, our work explains how they are actively sustained in adherent cells.
肌动蛋白动力学维持粘附细胞膜张力的空间梯度
张力在脂质双层膜中的传播速度极快,因此无法形成张力梯度。然而,在迁移细胞和轴突上已经证明了质膜张力梯度。在这里,我们使用荧光膜张力探针证明,无论细胞是否迁移,所有粘附细胞中都存在膜张力梯度。非粘附细胞不显示张力梯度。我们进一步发现,分枝肌动蛋白会增加张力,而膜与皮层的附着会促进张力的传播。粘附点边缘的张力最低,突起处的张力最高,从而确定了张力梯度的边界。通过提供膜张力梯度组织背后的定量和机理基础,我们的工作解释了如何在粘附细胞中积极维持膜张力梯度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信