Effects of substrate stiffness on cell morphology, cytoskeletal structure, and adhesion

被引:1805
作者
Yeung, T
Georges, PC
Flanagan, LA
Marg, B
Ortiz, M
Funaki, M
Zahir, N
Ming, WY
Weaver, V
Janmey, PA
机构
[1] Univ Penn, IME, Vagelos Labs 1010, Philadelphia, PA 19104 USA
[2] Brigham & Womens Hosp, Div Hematol, Boston, MA 02115 USA
来源
CELL MOTILITY AND THE CYTOSKELETON | 2005年 / 60卷 / 01期
关键词
substrate stiffness; cell morphology; fibroblasts; mechanosensing; cell-matrix interaction; actin cytoskeleton; integrin expression;
D O I
10.1002/cm.20041
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 alpha5 integrin also occurs in the same stiffness range, but exogenous expression of a5 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. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:24 / 34
页数:11
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