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A Robust Actin Filaments Image Analysis Framework

The cytoskeleton is a highly dynamical protein network that plays a central role in numerous cellular physiological processes, and is traditionally divided into three components according to its chemical composition, i.e. actin, tubulin and intermediate filament cytoskeletons. Understanding the cyto...

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Autores principales: Alioscha-Perez, Mitchel, Benadiba, Carine, Goossens, Katty, Kasas, Sandor, Dietler, Giovanni, Willaert, Ronnie, Sahli, Hichem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995035/
https://www.ncbi.nlm.nih.gov/pubmed/27551746
http://dx.doi.org/10.1371/journal.pcbi.1005063
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author Alioscha-Perez, Mitchel
Benadiba, Carine
Goossens, Katty
Kasas, Sandor
Dietler, Giovanni
Willaert, Ronnie
Sahli, Hichem
author_facet Alioscha-Perez, Mitchel
Benadiba, Carine
Goossens, Katty
Kasas, Sandor
Dietler, Giovanni
Willaert, Ronnie
Sahli, Hichem
author_sort Alioscha-Perez, Mitchel
collection PubMed
description The cytoskeleton is a highly dynamical protein network that plays a central role in numerous cellular physiological processes, and is traditionally divided into three components according to its chemical composition, i.e. actin, tubulin and intermediate filament cytoskeletons. Understanding the cytoskeleton dynamics is of prime importance to unveil mechanisms involved in cell adaptation to any stress type. Fluorescence imaging of cytoskeleton structures allows analyzing the impact of mechanical stimulation in the cytoskeleton, but it also imposes additional challenges in the image processing stage, such as the presence of imaging-related artifacts and heavy blurring introduced by (high-throughput) automated scans. However, although there exists a considerable number of image-based analytical tools to address the image processing and analysis, most of them are unfit to cope with the aforementioned challenges. Filamentous structures in images can be considered as a piecewise composition of quasi-straight segments (at least in some finer or coarser scale). Based on this observation, we propose a three-steps actin filaments extraction methodology: (i) first the input image is decomposed into a ‘cartoon’ part corresponding to the filament structures in the image, and a noise/texture part, (ii) on the ‘cartoon’ image, we apply a multi-scale line detector coupled with a (iii) quasi-straight filaments merging algorithm for fiber extraction. The proposed robust actin filaments image analysis framework allows extracting individual filaments in the presence of noise, artifacts and heavy blurring. Moreover, it provides numerous parameters such as filaments orientation, position and length, useful for further analysis. Cell image decomposition is relatively under-exploited in biological images processing, and our study shows the benefits it provides when addressing such tasks. Experimental validation was conducted using publicly available datasets, and in osteoblasts grown in two different conditions: static (control) and fluid shear stress. The proposed methodology exhibited higher sensitivity values and similar accuracy compared to state-of-the-art methods.
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spelling pubmed-49950352016-09-12 A Robust Actin Filaments Image Analysis Framework Alioscha-Perez, Mitchel Benadiba, Carine Goossens, Katty Kasas, Sandor Dietler, Giovanni Willaert, Ronnie Sahli, Hichem PLoS Comput Biol Research Article The cytoskeleton is a highly dynamical protein network that plays a central role in numerous cellular physiological processes, and is traditionally divided into three components according to its chemical composition, i.e. actin, tubulin and intermediate filament cytoskeletons. Understanding the cytoskeleton dynamics is of prime importance to unveil mechanisms involved in cell adaptation to any stress type. Fluorescence imaging of cytoskeleton structures allows analyzing the impact of mechanical stimulation in the cytoskeleton, but it also imposes additional challenges in the image processing stage, such as the presence of imaging-related artifacts and heavy blurring introduced by (high-throughput) automated scans. However, although there exists a considerable number of image-based analytical tools to address the image processing and analysis, most of them are unfit to cope with the aforementioned challenges. Filamentous structures in images can be considered as a piecewise composition of quasi-straight segments (at least in some finer or coarser scale). Based on this observation, we propose a three-steps actin filaments extraction methodology: (i) first the input image is decomposed into a ‘cartoon’ part corresponding to the filament structures in the image, and a noise/texture part, (ii) on the ‘cartoon’ image, we apply a multi-scale line detector coupled with a (iii) quasi-straight filaments merging algorithm for fiber extraction. The proposed robust actin filaments image analysis framework allows extracting individual filaments in the presence of noise, artifacts and heavy blurring. Moreover, it provides numerous parameters such as filaments orientation, position and length, useful for further analysis. Cell image decomposition is relatively under-exploited in biological images processing, and our study shows the benefits it provides when addressing such tasks. Experimental validation was conducted using publicly available datasets, and in osteoblasts grown in two different conditions: static (control) and fluid shear stress. The proposed methodology exhibited higher sensitivity values and similar accuracy compared to state-of-the-art methods. Public Library of Science 2016-08-23 /pmc/articles/PMC4995035/ /pubmed/27551746 http://dx.doi.org/10.1371/journal.pcbi.1005063 Text en © 2016 Alioscha-Perez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Alioscha-Perez, Mitchel
Benadiba, Carine
Goossens, Katty
Kasas, Sandor
Dietler, Giovanni
Willaert, Ronnie
Sahli, Hichem
A Robust Actin Filaments Image Analysis Framework
title A Robust Actin Filaments Image Analysis Framework
title_full A Robust Actin Filaments Image Analysis Framework
title_fullStr A Robust Actin Filaments Image Analysis Framework
title_full_unstemmed A Robust Actin Filaments Image Analysis Framework
title_short A Robust Actin Filaments Image Analysis Framework
title_sort robust actin filaments image analysis framework
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995035/
https://www.ncbi.nlm.nih.gov/pubmed/27551746
http://dx.doi.org/10.1371/journal.pcbi.1005063
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