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Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows

Amoeboid cell motility is essential for a wide range of biological processes including wound healing, embryonic morphogenesis, and cancer metastasis. It relies on complex dynamical patterns of cell shape changes that pose long-standing challenges to mathematical modeling and raise a need for automat...

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Autores principales: Schindler, Daniel, Moldenhawer, Ted, Stange, Maike, Lepro, Valentino, Beta, Carsten, Holschneider, Matthias, Huisinga, Wilhelm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8412247/
https://www.ncbi.nlm.nih.gov/pubmed/34424898
http://dx.doi.org/10.1371/journal.pcbi.1009268
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author Schindler, Daniel
Moldenhawer, Ted
Stange, Maike
Lepro, Valentino
Beta, Carsten
Holschneider, Matthias
Huisinga, Wilhelm
author_facet Schindler, Daniel
Moldenhawer, Ted
Stange, Maike
Lepro, Valentino
Beta, Carsten
Holschneider, Matthias
Huisinga, Wilhelm
author_sort Schindler, Daniel
collection PubMed
description Amoeboid cell motility is essential for a wide range of biological processes including wound healing, embryonic morphogenesis, and cancer metastasis. It relies on complex dynamical patterns of cell shape changes that pose long-standing challenges to mathematical modeling and raise a need for automated and reproducible approaches to extract quantitative morphological features from image sequences. Here, we introduce a theoretical framework and a computational method for obtaining smooth representations of the spatiotemporal contour dynamics from stacks of segmented microscopy images. Based on a Gaussian process regression we propose a one-parameter family of regularized contour flows that allows us to continuously track reference points (virtual markers) between successive cell contours. We use this approach to define a coordinate system on the moving cell boundary and to represent different local geometric quantities in this frame of reference. In particular, we introduce the local marker dispersion as a measure to identify localized membrane expansions and provide a fully automated way to extract the properties of such expansions, including their area and growth time. The methods are available as an open-source software package called AmoePy, a Python-based toolbox for analyzing amoeboid cell motility (based on time-lapse microscopy data), including a graphical user interface and detailed documentation. Due to the mathematical rigor of our framework, we envision it to be of use for the development of novel cell motility models. We mainly use experimental data of the social amoeba Dictyostelium discoideum to illustrate and validate our approach.
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spelling pubmed-84122472021-09-03 Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows Schindler, Daniel Moldenhawer, Ted Stange, Maike Lepro, Valentino Beta, Carsten Holschneider, Matthias Huisinga, Wilhelm PLoS Comput Biol Research Article Amoeboid cell motility is essential for a wide range of biological processes including wound healing, embryonic morphogenesis, and cancer metastasis. It relies on complex dynamical patterns of cell shape changes that pose long-standing challenges to mathematical modeling and raise a need for automated and reproducible approaches to extract quantitative morphological features from image sequences. Here, we introduce a theoretical framework and a computational method for obtaining smooth representations of the spatiotemporal contour dynamics from stacks of segmented microscopy images. Based on a Gaussian process regression we propose a one-parameter family of regularized contour flows that allows us to continuously track reference points (virtual markers) between successive cell contours. We use this approach to define a coordinate system on the moving cell boundary and to represent different local geometric quantities in this frame of reference. In particular, we introduce the local marker dispersion as a measure to identify localized membrane expansions and provide a fully automated way to extract the properties of such expansions, including their area and growth time. The methods are available as an open-source software package called AmoePy, a Python-based toolbox for analyzing amoeboid cell motility (based on time-lapse microscopy data), including a graphical user interface and detailed documentation. Due to the mathematical rigor of our framework, we envision it to be of use for the development of novel cell motility models. We mainly use experimental data of the social amoeba Dictyostelium discoideum to illustrate and validate our approach. Public Library of Science 2021-08-23 /pmc/articles/PMC8412247/ /pubmed/34424898 http://dx.doi.org/10.1371/journal.pcbi.1009268 Text en © 2021 Schindler et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Schindler, Daniel
Moldenhawer, Ted
Stange, Maike
Lepro, Valentino
Beta, Carsten
Holschneider, Matthias
Huisinga, Wilhelm
Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows
title Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows
title_full Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows
title_fullStr Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows
title_full_unstemmed Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows
title_short Analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows
title_sort analysis of protrusion dynamics in amoeboid cell motility by means of regularized contour flows
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8412247/
https://www.ncbi.nlm.nih.gov/pubmed/34424898
http://dx.doi.org/10.1371/journal.pcbi.1009268
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