Stiffness-controlled three-dimensional extracellular matrices for high-resolution imaging of cell behavior

被引:166
作者
Fischer, Robert S. [1 ]
Myers, Kenneth A. [2 ]
Gardel, Margaret L. [3 ,4 ,5 ]
Waterman, Clare M. [1 ]
机构
[1] Natl Heart Lung & Blood Inst NHBLI, Cell Biol & Physiol Ctr, US Natl Inst Hlth NIH, Bethesda, MD USA
[2] Univ Sci, Dept Biol Sci, Philadelphia, PA USA
[3] Univ Chicago, James Franck Inst, Chicago, IL 60637 USA
[4] Inst Biophys Dynam, Chicago, IL USA
[5] Univ Chicago, Dept Phys, Chicago, IL 60637 USA
关键词
NEURITE OUTGROWTH; COLLAGEN; MIGRATION; CULTURE; SUBSTRATE; ADHESIONS; GROWTH; ANGIOGENESIS; CYTOSKELETON; FIBROBLASTS;
D O I
10.1038/nprot.2012.127
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of cell functions by the physical properties of the extracellular matrix (ECM) has emerged as a crucial contributor to development and disease. Two specific physical properties of the ECM, stiffness and dimensionality, each influence cell signaling and function. As these ECM physical properties are linked to other properties that also regulate cell behavior, e. g., integrin ligand density, parsing the specific contributions of ECM stiffness and dimensionality has proven difficult. Here we detail a simple protocol, which can be completed in 1-2 d, for combining three-dimensional (3D) ECM engagement with controlled underlying ECM stiffness. In these 'sandwich gels', cells are sandwiched between a 3D fibrillar ECM and an ECM-coupled polyacrylamide gel of defined compliance, allowing the study of the specific effects of ECM compliance on cell function in physiologically relevant 3D ECMs. This type of system enables high-resolution time-lapse imaging and is suitable for a wide range of cell types and molecular perturbations.
引用
收藏
页码:2056 / 2066
页数:11
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