High-Content Analysis of Cell Migration Dynamics within a Micropatterned Screening Platform

被引:1
作者
Almeida, Filipe, V [1 ]
Gammon, Luke [1 ]
Laly, Ana C. [1 ]
Pundel, Oscar J. [1 ]
Bishop, Cleo L. [1 ]
Connelly, John T. [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Ctr Cell Biol & Cutaneous Res, London, England
基金
英国生物技术与生命科学研究理事会;
关键词
animal replacement; cell migration; epigenetics; EZH2; high-throughput; COLLECTIVE MIGRATION; DIFFERENTIATION; INTEGRIN; ADHESION; GROWTH;
D O I
10.1002/adbi.201900011
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Cell migration is a fundamental biological process that is dynamically regulated by complex interactions between the microenvironment and intrinsic gene expression programs. Here, a high-throughput cell migration assay is developed using micropatterned and dynamically adhesive polymer brush substrates, which support highly precise and consistent control over cell-matrix interactions within a 96-well cell culture plate format. This system is combined with automated imaging and quantitation of both cell motility and organization of the F-actin cytoskeleton for high-content analysis of cell migration phenotypes. Using this platform to screen a library of 147 epigenetic inhibitors identifies a set of EZH2-specific compounds that promote cytoskeletal remodeling and accelerates keratinocyte migration through derepression of an epithelial to mesenchymal transition-like gene expression program. Together, these studies establish the high-throughput, micropatterned assay as a powerful tool for discovery of novel therapeutic targets and for dissecting complex gene-environment interactions involved in wound repair.
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页数:10
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