CASTILLA, Carlos, Martin MAŠKA, Dmitry SOROKIN, Erik MEIJERING and Carlos ORTIZ-DE-SOLÓRZANO. 3-D Quantification of Filopodia in Motile Cancer Cells. IEEE Transactions on Medical Imaging. IEEE, 2019, vol. 38, No 3, p. 862-872. ISSN 0278-0062. Available from: https://dx.doi.org/10.1109/TMI.2018.2873842.
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Basic information
Original name 3-D Quantification of Filopodia in Motile Cancer Cells
Authors CASTILLA, Carlos (724 Spain), Martin MAŠKA (203 Czech Republic, guarantor, belonging to the institution), Dmitry SOROKIN (643 Russian Federation, belonging to the institution), Erik MEIJERING (528 Netherlands) and Carlos ORTIZ-DE-SOLÓRZANO (724 Spain).
Edition IEEE Transactions on Medical Imaging, IEEE, 2019, 0278-0062.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10201 Computer sciences, information science, bioinformatics
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 6.685
RIV identification code RIV/00216224:14330/19:00107178
Organization unit Faculty of Informatics
Doi http://dx.doi.org/10.1109/TMI.2018.2873842
UT WoS 000460662400019
Keywords in English Filopodium segmentation and tracking;actin cytoskeleton;confocal microscopy;3D skeletonization;Chan-Vese model;convolutional neural network;deep learning
Tags cbia-web
Tags International impact, Reviewed
Changed by Changed by: RNDr. Pavel Šmerk, Ph.D., učo 3880. Changed: 12/4/2020 08:31.
Abstract
We present a 3D bioimage analysis workflow to quantitatively analyze single, actin-stained cells with filopodial protrusions of diverse structural and temporal attributes, such as number, length, thickness, level of branching, and lifetime, in time-lapse confocal microscopy image data. Our workflow makes use of convolutional neural networks trained using real as well as synthetic image data, to segment the cell volumes with highly heterogeneous fluorescence intensity levels and to detect individual filopodial protrusions, followed by a constrained nearest-neighbor tracking algorithm to obtain valuable information about the spatio-temporal evolution of individual filopodia. We validated the workflow using real and synthetic 3-D time-lapse sequences of lung adenocarcinoma cells of three morphologically distinct filopodial phenotypes and show that it achieves reliable segmentation and tracking performance, providing a robust, reproducible and less time-consuming alternative to manual analysis of the 3D+t image data.
Links
GJ16-03909Y, research and development projectName: Vývoj spolehlivých metod pro automatizovanou kvantitativní charakterizaci buněčné motility ve fluorescenční mikroskopii
Investor: Czech Science Foundation
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