Mapping of Mechanical Strains and Stresses around Quiescent Engineered Three-Dimensional Epithelial Tissues

被引:108
作者
Gjorevski, Nikolce [1 ]
Nelson, Celeste M. [1 ,2 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
基金
美国国家卫生研究院;
关键词
COLLECTIVE CELL-MIGRATION; MAMMARY-GLAND; BRANCHING MORPHOGENESIS; MATRIX REORGANIZATION; GEOMETRIC CONTROL; TRACTION FORCE; DIMENSIONS; ORGANIZATION; CONTRACTIONS; ELASTICITY;
D O I
10.1016/j.bpj.2012.05.048
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
Understanding how physical signals guide biological processes requires qualitative and quantitative knowledge of the mechanical forces generated and sensed by cells in a physiologically realistic three-dimensional (3D) context. Here, we used computational modeling and engineered epithelial tissues of precise geometry to define the experimental parameters that are required to measure directly the mechanical stress profile of 3D tissues embedded within native type I collagen. We found that to calculate the stresses accurately in these settings, we had to account for mechanical heterogeneities within the matrix, which we visualized and quantified using confocal reflectance and atomic force microscopy. Using this technique, we were able to obtain traction forces at the epithelium-matrix interface, and to resolve and quantify patterns of mechanical stress throughout the surrounding matrix. We discovered that whereas single cells generate tension by contracting and pulling on the matrix, the contraction of multicellular tissues can also push against the matrix, causing emergent compression. Furthermore, tissue geometry defines the spatial distribution of mechanical stress across the epithelium, which communicates mechanically over distances spanning hundreds of micrometers. Spatially resolved mechanical maps can provide insight into the types and magnitudes of physical parameters that are sensed and interpreted by multicellular tissues during normal and pathological processes.
引用
收藏
页码:152 / 162
页数:11
相关论文
共 60 条
[1]
Cell Migration Driven by Cooperative Substrate Deformation Patterns [J].
Angelini, Thomas E. ;
Hannezo, Edouard ;
Trepat, Xavier ;
Fredberg, Jeffrey J. ;
Weitz, David A. .
PHYSICAL REVIEW LETTERS, 2010, 104 (16)
[2]
THE FIBROBLAST-POPULATED COLLAGEN MICROSPHERE ASSAY OF CELL TRACTION FORCE .2. MEASUREMENT OF THE CELL TRACTION PARAMETER [J].
BAROCAS, VH ;
MOON, AG ;
TRANQUILLO, RT .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1995, 117 (02) :161-170
[3]
Cell organization in soft media due to active mechanosensing [J].
Bischofs, IB ;
Schwarz, US .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (16) :9274-9279
[4]
Mapping local matrix remodeling induced by a migrating tumor cell using three-dimensional multiple-particle tracking [J].
Bloom, Ryan J. ;
George, Jerry P. ;
Celedon, Alfredo ;
Sun, Sean X. ;
Wirtz, Denis .
BIOPHYSICAL JOURNAL, 2008, 95 (08) :4077-4088
[5]
Brightman AO, 2000, BIOPOLYMERS, V54, P222
[6]
Traction fields, moments, and strain energy that cells exert on their surroundings [J].
Butler, JP ;
Tolic-Norrelykke, IM ;
Fabry, B ;
Fredberg, JJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 282 (03) :C595-C605
[7]
Tip-Cell Migration Controls Stalk-Cell Intercalation during Drosophila Tracheal Tube Elongation [J].
Caussinus, Emmanuel ;
Colombelli, Julien ;
Affolter, Markus .
CURRENT BIOLOGY, 2008, 18 (22) :1727-1734
[8]
Geometric control of cell life and death [J].
Chen, CS ;
Mrksich, M ;
Huang, S ;
Whitesides, GM ;
Ingber, DE .
SCIENCE, 1997, 276 (5317) :1425-1428
[9]
Taking cell-matrix adhesions to the third dimension [J].
Cukierman, E ;
Pankov, R ;
Stevens, DR ;
Yamada, KM .
SCIENCE, 2001, 294 (5547) :1708-1712
[10]
The Role of TGF-β in Patterning and Growth of the Mammary Ductal Tree [J].
Daniel, Charles W. ;
Robinson, Stephen ;
Silberstein, Gary B. .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 1996, 1 (04) :331-341