Techniques for assessing 3-D cell-matrix mechanical interactions in vitro and in vivo

被引:20
作者
Miron-Mendoza, Miguel [1 ]
Koppaka, Vindhya [1 ]
Zhou, Chengxin [1 ,2 ]
Petroll, W. Matthew [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Ophthalmol, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Grad Program Biomed Engn, Dallas, TX 75390 USA
关键词
Cell mechanics; Cell migration; Extracellular matrix; Microscopy; NONLINEAR-OPTICAL MICROSCOPY; EXTRACELLULAR-MATRIX; MULTIPHOTON MICROSCOPY; 2ND-HARMONIC GENERATION; COLLAGEN-MATRIX; CONTACT GUIDANCE; CORNEAL FIBROBLASTS; TENSIONAL HOMEOSTASIS; SUBSTRATE TOPOGRAPHY; DYNAMIC ASSESSMENT;
D O I
10.1016/j.yexcr.2013.06.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cellular interactions with extracellular matrices (ECM) through the application of mechanical forces mediate numerous biological processes including developmental morphogenesis, wound healing and cancer metastasis. They also play a key role in the cellular repopulation and/or remodeling of engineered tissues and organs. While 2-D studies can provide important insights into many aspects of cellular mechanobiology, cells reside within 3-D ECMs in vivo, and matrix structure and dimensionality have been shown to impact cell morphology, protein organization and mechanical behavior. Global measurements of cell-induced compaction of 3-D collagen matrices can provide important insights into the regulation of overall cell contractility by various cytokines and signaling pathways. However, to understand how the mechanics of cell spreading, migration, contraction and matrix remodeling are regulated at the molecular level, these processes must also be studied in individual cells. Here we review the evolution and application of techniques for imaging and assessing local cell matrix mechanical interactions in 3-D culture models, tissue explants and living animals. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:2470 / 2480
页数:11
相关论文
共 160 条
[21]   Multiphoton excitation provides optical sections from deeper within scattering specimens than confocal imaging [J].
Centonze, VE ;
White, JG .
BIOPHYSICAL JOURNAL, 1998, 75 (04) :2015-2024
[22]   Affine versus non-affine fibril kinematics in collagen networks: Theoretical studies of network behavior [J].
Chandran, PL ;
Barocas, VH .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 2006, 128 (02) :259-270
[23]   3-D in vitro model of early skeletal muscle development [J].
Cheema, U ;
Yang, SY ;
Mudera, V ;
Goldspink, GG ;
Brown, RA .
CELL MOTILITY AND THE CYTOSKELETON, 2003, 54 (03) :226-236
[24]   Spectral characteristics of autofluorescence and second harmonic generation from ex vivo human skin induced by femtosecond laser and visible lasers [J].
Chen, Jianxin ;
Zhuo, Shuangmu ;
Luo, Tianshu ;
Jiang, Xingshan ;
Zhao, Jingjun .
SCANNING, 2006, 28 (06) :319-326
[25]   Second harmonic generation microscopy for quantitative analysis of collagen fibrillar structure [J].
Chen, Xiyi ;
Nadiarynkh, Oleg ;
Plotnikov, Sergey ;
Campagnola, Paul J. .
NATURE PROTOCOLS, 2012, 7 (04) :654-669
[26]   Intravital imaging of cell movement in tumours [J].
Condeelis, J ;
Segall, JE .
NATURE REVIEWS CANCER, 2003, 3 (12) :921-930
[27]   The great escape: When cancer cells hijack the genes for chemotaxis and motility [J].
Condeelis, J ;
Singer, RH ;
Segall, JE .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2005, 21 :695-718
[28]   In Vivo Imaging in Cancer [J].
Condeelis, John ;
Weissleder, Ralph .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2010, 2 (12) :a003848
[29]   Taking cell-matrix adhesions to the third dimension [J].
Cukierman, E ;
Pankov, R ;
Stevens, DR ;
Yamada, KM .
SCIENCE, 2001, 294 (5547) :1708-1712
[30]   Fibroblast cluster formation on 3D collagen matrices requires cell contraction dependent fibronectin matrix organization [J].
da Rocha-Azevedo, Bruno ;
Ho, Chin-Han ;
Grinnell, Frederick .
EXPERIMENTAL CELL RESEARCH, 2013, 319 (04) :546-555