FibrilTool, an ImageJ plug-in to quantify fibrillar structures in raw microscopy images

被引:455
作者
Boudaoud, Arezki [1 ,2 ]
Burian, Agata [3 ]
Borowska-Wykret, Dorota [3 ]
Uyttewaal, Magalie [1 ,4 ]
Wrzalik, Roman [5 ]
Kwiatkowska, Dorota [3 ]
Hamant, Olivier [1 ,2 ]
机构
[1] Univ Lyon, Ecole Normale Super Lyon, CNRS, INRA,Lab Reprod & Dev Plantes, Lyon, France
[2] Univ Lyon 1, ENS Lyon, CNRS, Lab Joliot Curie, F-69365 Lyon, France
[3] Silesian Univ, Dept Biophys & Morphogenesis Plants, Katowice, Poland
[4] AgroParisTech, INRA, UMR1318, Inst Jean Pierre Bourgin,Ctr Versailles, Versailles, France
[5] Silesian Univ, August Chelkowski Inst Phys, Katowice, Poland
关键词
FLUORESCENCE MICROSCOPY; ORIENTATION; GROWTH; QUANTIFICATION;
D O I
10.1038/nprot.2014.024
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Cell biology heavily relies on the behavior of fibrillar structures, such as the cytoskeleton, yet the analysis of their behavior in tissues often remains qualitative. Image analysis tools have been developed to quantify this behavior, but they often involve an image pre-processing stage that may bias the output and/or they require specific software. Here we describe FibrilTool, an ImageJ plug-in based on the concept of nematic tensor, which can provide a quantitative description of the anisotropy of fiber arrays and their average orientation in cells, directly from raw images obtained by any form of microscopy. FibrilTool has been validated on microtubules, actin and cellulose microfibrils, but it may also help analyze other fibrillar structures, such as collagen, or the texture of various materials. The tool is ImageJ-based, and it is therefore freely accessible to the scientific community and does not require specific computational setup. The tool provides the average orientation and anisotropy of fiber arrays in a given region of interest (ROI) in a few seconds.
引用
收藏
页码:457 / 463
页数:7
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