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Effects of substrate stiffness on cell morphology, cytoskeletal structure, and adhesion
The morphology and cytoskeletal structure of fibroblasts, endothelial cells, and neutrophils are documented for cells cultured on surfaces with stiffness ranging from 2 to 55,000 Pa that have been laminated with fibronectin or collagen as adhesive ligand. When grown in sparse culture with no cell‐ce...
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Published in: | Cell motility and the cytoskeleton 2005-01, Vol.60 (1), p.24-34 |
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container_title | Cell motility and the cytoskeleton |
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creator | Yeung, Tony Georges, Penelope C. Flanagan, Lisa A. Marg, Beatrice Ortiz, Miguelina Funaki, Makoto Zahir, Nastaran Ming, Wenyu Weaver, Valerie Janmey, Paul A. |
description | The morphology and cytoskeletal structure of fibroblasts, endothelial cells, and neutrophils are documented for cells cultured on surfaces with stiffness ranging from 2 to 55,000 Pa that have been laminated with fibronectin or collagen as adhesive ligand. When grown in sparse culture with no cell‐cell contacts, fibroblasts and endothelial cells show an abrupt change in spread area that occurs at a stiffness range around 3,000 Pa. No actin stress fibers are seen in fibroblasts on soft surfaces, and the appearance of stress fibers is abrupt and complete at a stiffness range coincident with that at which they spread. Upregulation of α5 integrin also occurs in the same stiffness range, but exogenous expression of α5 integrin is not sufficient to cause cell spreading on soft surfaces. Neutrophils, in contrast, show no dependence of either resting shape or ability to spread after activation when cultured on surfaces as soft as 2 Pa compared to glass. The shape and cytoskeletal differences evident in single cells on soft compared to hard substrates are eliminated when fibroblasts or endothelial cells make cell‐cell contact. These results support the hypothesis that mechanical factors impact different cell types in fundamentally different ways, and can trigger specific changes similar to those stimulated by soluble ligands. Cell Motil. Cytoskeleton 60:24–34, 2005. © 2004 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/cm.20041 |
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When grown in sparse culture with no cell‐cell contacts, fibroblasts and endothelial cells show an abrupt change in spread area that occurs at a stiffness range around 3,000 Pa. No actin stress fibers are seen in fibroblasts on soft surfaces, and the appearance of stress fibers is abrupt and complete at a stiffness range coincident with that at which they spread. Upregulation of α5 integrin also occurs in the same stiffness range, but exogenous expression of α5 integrin is not sufficient to cause cell spreading on soft surfaces. Neutrophils, in contrast, show no dependence of either resting shape or ability to spread after activation when cultured on surfaces as soft as 2 Pa compared to glass. The shape and cytoskeletal differences evident in single cells on soft compared to hard substrates are eliminated when fibroblasts or endothelial cells make cell‐cell contact. These results support the hypothesis that mechanical factors impact different cell types in fundamentally different ways, and can trigger specific changes similar to those stimulated by soluble ligands. Cell Motil. Cytoskeleton 60:24–34, 2005. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 0886-1544</identifier><identifier>EISSN: 1097-0169</identifier><identifier>DOI: 10.1002/cm.20041</identifier><identifier>PMID: 15573414</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>actin cytoskeleton ; Actins - metabolism ; Animals ; Aorta - cytology ; Cattle ; Cell Adhesion ; Cell Line ; cell morphology ; cell-matrix interaction ; Cells, Cultured ; Collagen - metabolism ; Cytoskeleton - metabolism ; Endothelium, Vascular - cytology ; Endothelium, Vascular - physiology ; Extracellular Matrix - metabolism ; fibroblasts ; Fibroblasts - cytology ; Fibroblasts - physiology ; Fibronectins - metabolism ; Glass ; Green Fluorescent Proteins - metabolism ; Humans ; Integrin alpha5 - metabolism ; integrin expression ; mechanosensing ; Mice ; Microscopy, Confocal ; Neutrophils - cytology ; Neutrophils - physiology ; NIH 3T3 Cells ; Stress Fibers ; substrate stiffness ; Surface Properties</subject><ispartof>Cell motility and the cytoskeleton, 2005-01, Vol.60 (1), p.24-34</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>Copyright 2004 Wiley-Liss, Inc.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4961-651f674d5cc9e9e1fca66d987bb7e9365748907d863dc13ea75a534508b5735b3</citedby><cites>FETCH-LOGICAL-c4961-651f674d5cc9e9e1fca66d987bb7e9365748907d863dc13ea75a534508b5735b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15573414$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yeung, Tony</creatorcontrib><creatorcontrib>Georges, Penelope C.</creatorcontrib><creatorcontrib>Flanagan, Lisa A.</creatorcontrib><creatorcontrib>Marg, Beatrice</creatorcontrib><creatorcontrib>Ortiz, Miguelina</creatorcontrib><creatorcontrib>Funaki, Makoto</creatorcontrib><creatorcontrib>Zahir, Nastaran</creatorcontrib><creatorcontrib>Ming, Wenyu</creatorcontrib><creatorcontrib>Weaver, Valerie</creatorcontrib><creatorcontrib>Janmey, Paul A.</creatorcontrib><title>Effects of substrate stiffness on cell morphology, cytoskeletal structure, and adhesion</title><title>Cell motility and the cytoskeleton</title><addtitle>Cell Motil. Cytoskeleton</addtitle><description>The morphology and cytoskeletal structure of fibroblasts, endothelial cells, and neutrophils are documented for cells cultured on surfaces with stiffness ranging from 2 to 55,000 Pa that have been laminated with fibronectin or collagen as adhesive ligand. When grown in sparse culture with no cell‐cell contacts, fibroblasts and endothelial cells show an abrupt change in spread area that occurs at a stiffness range around 3,000 Pa. No actin stress fibers are seen in fibroblasts on soft surfaces, and the appearance of stress fibers is abrupt and complete at a stiffness range coincident with that at which they spread. Upregulation of α5 integrin also occurs in the same stiffness range, but exogenous expression of α5 integrin is not sufficient to cause cell spreading on soft surfaces. Neutrophils, in contrast, show no dependence of either resting shape or ability to spread after activation when cultured on surfaces as soft as 2 Pa compared to glass. The shape and cytoskeletal differences evident in single cells on soft compared to hard substrates are eliminated when fibroblasts or endothelial cells make cell‐cell contact. These results support the hypothesis that mechanical factors impact different cell types in fundamentally different ways, and can trigger specific changes similar to those stimulated by soluble ligands. Cell Motil. Cytoskeleton 60:24–34, 2005. © 2004 Wiley‐Liss, Inc.</description><subject>actin cytoskeleton</subject><subject>Actins - metabolism</subject><subject>Animals</subject><subject>Aorta - cytology</subject><subject>Cattle</subject><subject>Cell Adhesion</subject><subject>Cell Line</subject><subject>cell morphology</subject><subject>cell-matrix interaction</subject><subject>Cells, Cultured</subject><subject>Collagen - metabolism</subject><subject>Cytoskeleton - metabolism</subject><subject>Endothelium, Vascular - cytology</subject><subject>Endothelium, Vascular - physiology</subject><subject>Extracellular Matrix - metabolism</subject><subject>fibroblasts</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - physiology</subject><subject>Fibronectins - metabolism</subject><subject>Glass</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Humans</subject><subject>Integrin alpha5 - metabolism</subject><subject>integrin expression</subject><subject>mechanosensing</subject><subject>Mice</subject><subject>Microscopy, Confocal</subject><subject>Neutrophils - cytology</subject><subject>Neutrophils - physiology</subject><subject>NIH 3T3 Cells</subject><subject>Stress Fibers</subject><subject>substrate stiffness</subject><subject>Surface Properties</subject><issn>0886-1544</issn><issn>1097-0169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp10E1P3DAQBmALteoutFJ_AcoJcSBgr7_iY7XiS9CiIhCoF8txxmwgiRfbUcm_J8su5dTTSKNHr2ZehL4TfEgwnh3Z9nCGMSNbaEqwkjkmQn1CU1wUIiecsQnajvERY0KY5F_QhHAuKSNsiu6OnQObYuZdFvsypmASZDHVznUQx3WXWWiarPVhufCNfxgOMjskH5-ggWSakYbepj7AQWa6KjPVAmLtu6_oszNNhG-buYNuT45v5mf55dXp-fzHZW6ZEiQXnDghWcWtVaCAOGuEqFQhy1KCooJLVigsq0LQyhIKRnLDKeO4KMcPeEl30N46dxn8cw8x6baOq4tNB76PWkhKZ4qLEe6voQ0-xgBOL0PdmjBogvWqRG1b_VbiSHc3mX3ZQvUBN62NIF-Dv3UDw3-D9Pzne-DG1zHByz9vwtPqPsn13a9TLW7ur_-cXRD9m74CGkeJxQ</recordid><startdate>200501</startdate><enddate>200501</enddate><creator>Yeung, Tony</creator><creator>Georges, Penelope C.</creator><creator>Flanagan, Lisa A.</creator><creator>Marg, Beatrice</creator><creator>Ortiz, Miguelina</creator><creator>Funaki, Makoto</creator><creator>Zahir, Nastaran</creator><creator>Ming, Wenyu</creator><creator>Weaver, Valerie</creator><creator>Janmey, Paul A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200501</creationdate><title>Effects of substrate stiffness on cell morphology, cytoskeletal structure, and adhesion</title><author>Yeung, Tony ; 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Cytoskeleton</addtitle><date>2005-01</date><risdate>2005</risdate><volume>60</volume><issue>1</issue><spage>24</spage><epage>34</epage><pages>24-34</pages><issn>0886-1544</issn><eissn>1097-0169</eissn><abstract>The morphology and cytoskeletal structure of fibroblasts, endothelial cells, and neutrophils are documented for cells cultured on surfaces with stiffness ranging from 2 to 55,000 Pa that have been laminated with fibronectin or collagen as adhesive ligand. When grown in sparse culture with no cell‐cell contacts, fibroblasts and endothelial cells show an abrupt change in spread area that occurs at a stiffness range around 3,000 Pa. No actin stress fibers are seen in fibroblasts on soft surfaces, and the appearance of stress fibers is abrupt and complete at a stiffness range coincident with that at which they spread. Upregulation of α5 integrin also occurs in the same stiffness range, but exogenous expression of α5 integrin is not sufficient to cause cell spreading on soft surfaces. Neutrophils, in contrast, show no dependence of either resting shape or ability to spread after activation when cultured on surfaces as soft as 2 Pa compared to glass. The shape and cytoskeletal differences evident in single cells on soft compared to hard substrates are eliminated when fibroblasts or endothelial cells make cell‐cell contact. These results support the hypothesis that mechanical factors impact different cell types in fundamentally different ways, and can trigger specific changes similar to those stimulated by soluble ligands. Cell Motil. Cytoskeleton 60:24–34, 2005. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15573414</pmid><doi>10.1002/cm.20041</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | actin cytoskeleton Actins - metabolism Animals Aorta - cytology Cattle Cell Adhesion Cell Line cell morphology cell-matrix interaction Cells, Cultured Collagen - metabolism Cytoskeleton - metabolism Endothelium, Vascular - cytology Endothelium, Vascular - physiology Extracellular Matrix - metabolism fibroblasts Fibroblasts - cytology Fibroblasts - physiology Fibronectins - metabolism Glass Green Fluorescent Proteins - metabolism Humans Integrin alpha5 - metabolism integrin expression mechanosensing Mice Microscopy, Confocal Neutrophils - cytology Neutrophils - physiology NIH 3T3 Cells Stress Fibers substrate stiffness Surface Properties |
title | Effects of substrate stiffness on cell morphology, cytoskeletal structure, and adhesion |
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