Open source software for quantification of cell migration, protrusions, and fluorescence intensities

被引:115
作者
Barry, David J. [1 ]
Durkin, Charlotte H. [1 ]
Abella, Jasmine V. [1 ]
Way, Michael [1 ]
机构
[1] Francis Crick Inst, Lincolns Inn Fields Labs, London WC2A 3LY, England
基金
加拿大健康研究院;
关键词
ARP2/3; COMPLEX; F-ACTIN; BLEBS; LAMELLIPODIA; TRACKING; CORTEX; HOMEOSTASIS; INHIBITION; MOVEMENT; PROTEINS;
D O I
10.1083/jcb.201501081
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell migration is frequently accompanied by changes in cell morphology (morphodynamics) on a range of spatial and temporal scales. Despite recent advances in imaging techniques, the application of unbiased computational image analysis methods for morphodynamic quantification is rare. For example, manual analysis using kymographs is still commonplace, often caused by lack of access to user-friendly, automated tools. We now describe software designed for the automated quantification of cell migration and morphodynamics. Implemented as a plug-in for the open-source platform, ImageJ, ADAPT is capable of rapid, automated analysis of migration and membrane protrusions, together with associated fluorescently labeled proteins, across multiple cells. We demonstrate the ability of the software by quantifying variations in cell population migration rates on different extracellular matrices. We also show that ADAPT can detect and morphologically profile filopodia. Finally, we have used ADAPT to compile an unbiased description of a "typical" bleb formed at the plasma membrane and quantify the effect of Arp2/3 complex inhibition on bleb retraction.
引用
收藏
页码:163 / 180
页数:18
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