Critical centrifugal forces induce adhesion rupture or structural reorganization in cultured cells.

O Thoumine, A Ott, D Louvard
{"title":"Critical centrifugal forces induce adhesion rupture or structural reorganization in cultured cells.","authors":"O Thoumine,&nbsp;A Ott,&nbsp;D Louvard","doi":"10.1002/(SICI)1097-0169(1996)33:4<276::AID-CM4>3.0.CO;2-7","DOIUrl":null,"url":null,"abstract":"<p><p>Cultured epithelial cells were exposed to accelerations ranging from 9,000 to 70,000g for time periods of 5, 15, or 60 min, by centrifugation in a direction tangential to their plastic substrate. Three regimes describe the cellular response: (1) Cell morphology and density remain unaltered at forces below a threshold of about 10(-7) N; (2) Between this critical force and a second threshold of about 1.5 10(-7)N, the number of adherent cells decreases exponentially with time and acceleration, with no alteration of cell morphology. This behavior can be modeled by a constant probability of detaching and by an exponential distribution of cell-to-substrate adhesive forces; (3) Past the second threshold, cells that are still adherent exhibit elongated morphologies, the degree of elongation increasing linearly with the force. The fact that cells lose their vinculin-rich focal contacts past the first threshold and that cells cultured on gelatin-coated plastic show an increased resistance to detachment suggests a rupture of cell-to-substrate adhesions upon centrifugation. Immunofluorescent labeling of cells for actin and tubulin shows a reorganization of the cytoskeleton upon centrifugation, and treatment of cells with the drugs cytochalasin D and nocodazole demonstrates that cytoskeletal elements are actively involved in the structural deformation of cells past the second acceleration threshold, microtubules and microfilaments paying antagonistic roles.</p>","PeriodicalId":9675,"journal":{"name":"Cell motility and the cytoskeleton","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/(SICI)1097-0169(1996)33:4<276::AID-CM4>3.0.CO;2-7","citationCount":"61","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell motility and the cytoskeleton","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/(SICI)1097-0169(1996)33:4<276::AID-CM4>3.0.CO;2-7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 61

Abstract

Cultured epithelial cells were exposed to accelerations ranging from 9,000 to 70,000g for time periods of 5, 15, or 60 min, by centrifugation in a direction tangential to their plastic substrate. Three regimes describe the cellular response: (1) Cell morphology and density remain unaltered at forces below a threshold of about 10(-7) N; (2) Between this critical force and a second threshold of about 1.5 10(-7)N, the number of adherent cells decreases exponentially with time and acceleration, with no alteration of cell morphology. This behavior can be modeled by a constant probability of detaching and by an exponential distribution of cell-to-substrate adhesive forces; (3) Past the second threshold, cells that are still adherent exhibit elongated morphologies, the degree of elongation increasing linearly with the force. The fact that cells lose their vinculin-rich focal contacts past the first threshold and that cells cultured on gelatin-coated plastic show an increased resistance to detachment suggests a rupture of cell-to-substrate adhesions upon centrifugation. Immunofluorescent labeling of cells for actin and tubulin shows a reorganization of the cytoskeleton upon centrifugation, and treatment of cells with the drugs cytochalasin D and nocodazole demonstrates that cytoskeletal elements are actively involved in the structural deformation of cells past the second acceleration threshold, microtubules and microfilaments paying antagonistic roles.

临界离心力诱导培养细胞粘附破裂或结构重组。
将培养的上皮细胞暴露在9000至70000 g的加速度下,离心5、15或60分钟,方向与塑料底物相切。三种机制描述了细胞的反应:(1)当力低于10(-7)N的阈值时,细胞形态和密度保持不变;(2)在该临界力和第二阈值(约1.5 10(-7)N)之间,贴壁细胞数量随时间和加速度呈指数减少,细胞形态没有改变。这种行为可以通过恒定的分离概率和细胞-基质粘附力的指数分布来建模;(3)超过第二个阈值后,仍然贴壁的细胞表现出伸长的形态,伸长的程度随着力的增加而线性增加。事实上,细胞在第一个阈值之后就失去了富含白细胞素的局部接触,并且在明胶包覆塑料上培养的细胞对脱离的抵抗力增强,这表明在离心时细胞与底物的粘附破裂。对细胞进行肌动蛋白和微管蛋白的免疫荧光标记显示,细胞骨架在离心后发生了重组,用细胞松弛素D和诺可达唑处理细胞表明,细胞骨架元件积极参与细胞超过第二加速阈值的结构变形,微管和微丝发挥拮抗作用。
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