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Automated characterization of cell shape changes during amoeboid motility by skeletonization

BACKGROUND: The ability of a cell to change shape is crucial for the proper function of many cellular processes, including cell migration. One type of cell migration, referred to as amoeboid motility, involves alternating cycles of morphological expansion and retraction. Traditionally, this process...

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Autores principales: Xiong, Yuan, Kabacoff, Cathryn, Franca-Koh, Jonathan, Devreotes, Peter N, Robinson, Douglas N, Iglesias, Pablo A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864235/
https://www.ncbi.nlm.nih.gov/pubmed/20334652
http://dx.doi.org/10.1186/1752-0509-4-33
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author Xiong, Yuan
Kabacoff, Cathryn
Franca-Koh, Jonathan
Devreotes, Peter N
Robinson, Douglas N
Iglesias, Pablo A
author_facet Xiong, Yuan
Kabacoff, Cathryn
Franca-Koh, Jonathan
Devreotes, Peter N
Robinson, Douglas N
Iglesias, Pablo A
author_sort Xiong, Yuan
collection PubMed
description BACKGROUND: The ability of a cell to change shape is crucial for the proper function of many cellular processes, including cell migration. One type of cell migration, referred to as amoeboid motility, involves alternating cycles of morphological expansion and retraction. Traditionally, this process has been characterized by a number of parameters providing global information about shape changes, which are insufficient to distinguish phenotypes based on local pseudopodial activities that typify amoeboid motility. RESULTS: We developed a method that automatically detects and characterizes pseudopodial behavior of cells. The method uses skeletonization, a technique from morphological image processing to reduce a shape into a series of connected lines. It involves a series of automatic algorithms including image segmentation, boundary smoothing, skeletonization and branch pruning, and takes into account the cell shape changes between successive frames to detect protrusion and retraction activities. In addition, the activities are clustered into different groups, each representing the protruding and retracting history of an individual pseudopod. CONCLUSIONS: We illustrate the algorithms on movies of chemotaxing Dictyostelium cells and show that our method makes it possible to capture the spatial and temporal dynamics as well as the stochastic features of the pseudopodial behavior. Thus, the method provides a powerful tool for investigating amoeboid motility.
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spelling pubmed-28642352010-05-05 Automated characterization of cell shape changes during amoeboid motility by skeletonization Xiong, Yuan Kabacoff, Cathryn Franca-Koh, Jonathan Devreotes, Peter N Robinson, Douglas N Iglesias, Pablo A BMC Syst Biol Methodology article BACKGROUND: The ability of a cell to change shape is crucial for the proper function of many cellular processes, including cell migration. One type of cell migration, referred to as amoeboid motility, involves alternating cycles of morphological expansion and retraction. Traditionally, this process has been characterized by a number of parameters providing global information about shape changes, which are insufficient to distinguish phenotypes based on local pseudopodial activities that typify amoeboid motility. RESULTS: We developed a method that automatically detects and characterizes pseudopodial behavior of cells. The method uses skeletonization, a technique from morphological image processing to reduce a shape into a series of connected lines. It involves a series of automatic algorithms including image segmentation, boundary smoothing, skeletonization and branch pruning, and takes into account the cell shape changes between successive frames to detect protrusion and retraction activities. In addition, the activities are clustered into different groups, each representing the protruding and retracting history of an individual pseudopod. CONCLUSIONS: We illustrate the algorithms on movies of chemotaxing Dictyostelium cells and show that our method makes it possible to capture the spatial and temporal dynamics as well as the stochastic features of the pseudopodial behavior. Thus, the method provides a powerful tool for investigating amoeboid motility. BioMed Central 2010-03-24 /pmc/articles/PMC2864235/ /pubmed/20334652 http://dx.doi.org/10.1186/1752-0509-4-33 Text en Copyright ©2010 Xiong et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology article
Xiong, Yuan
Kabacoff, Cathryn
Franca-Koh, Jonathan
Devreotes, Peter N
Robinson, Douglas N
Iglesias, Pablo A
Automated characterization of cell shape changes during amoeboid motility by skeletonization
title Automated characterization of cell shape changes during amoeboid motility by skeletonization
title_full Automated characterization of cell shape changes during amoeboid motility by skeletonization
title_fullStr Automated characterization of cell shape changes during amoeboid motility by skeletonization
title_full_unstemmed Automated characterization of cell shape changes during amoeboid motility by skeletonization
title_short Automated characterization of cell shape changes during amoeboid motility by skeletonization
title_sort automated characterization of cell shape changes during amoeboid motility by skeletonization
topic Methodology article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864235/
https://www.ncbi.nlm.nih.gov/pubmed/20334652
http://dx.doi.org/10.1186/1752-0509-4-33
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