Multiplex Profiling of Cellular Invasion in 3D Cell Culture Models

被引:29
作者
Burgstaller, Gerald [1 ,2 ]
Oehrle, Bettina [1 ,2 ]
Koch, Ina [3 ]
Lindner, Michael [3 ]
Eickelberg, Oliver [1 ,2 ]
机构
[1] Univ Munich, Univ Hosp, Comprehens Pneumol Ctr, Munich, Germany
[2] Helmholtz Zentrum Munchen, Munich, Germany
[3] Asklepios Clin Munich Gauting, Comprehens Pneumol Ctr, Asklepios Biobank Lung Dis, Ctr Thorac Surg, Munich, Germany
关键词
EPIDERMAL-GROWTH-FACTOR; FIBROBLAST MIGRATION; EXTRACELLULAR-MATRIX; MORPHOLOGY; EXPRESSION; ADHESIONS;
D O I
10.1371/journal.pone.0063121
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To-date, most invasion or migration assays use a modified Boyden chamber-like design to assess migration as single-cell or scratch assays on coated or uncoated planar plastic surfaces. Here, we describe a 96-well microplate-based, high-content, three-dimensional cell culture assay capable of assessing invasion dynamics and molecular signatures thereof. On applying our invasion assay, we were able to demonstrate significant effects on the invasion capacity of fibroblast cell lines, as well as primary lung fibroblasts. Administration of epidermal growth factor resulted in a substantial increase of cellular invasion, thus making this technique suitable for high-throughput pharmacological screening of novel compounds regulating invasive and migratory pathways of primary cells. Our assay also correlates cellular invasiveness to molecular events. Thus, we argue of having developed a powerful and versatile toolbox for an extensive profiling of invasive cells in a 96-well format. This will have a major impact on research in disease areas like fibrosis, metastatic cancers, or chronic inflammatory states.
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页数:9
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