Cargando…
Open source software for quantification of cell migration, protrusions, and fluorescence intensities
Cell migration is frequently accompanied by changes in cell morphology (morphodynamics) on a range of spatial and temporal scales. Despite recent advances in imaging techniques, the application of unbiased computational image analysis methods for morphodynamic quantification is rare. For example, ma...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4395480/ https://www.ncbi.nlm.nih.gov/pubmed/25847537 http://dx.doi.org/10.1083/jcb.201501081 |
_version_ | 1782366457181503488 |
---|---|
author | Barry, David J. Durkin, Charlotte H. Abella, Jasmine V. Way, Michael |
author_facet | Barry, David J. Durkin, Charlotte H. Abella, Jasmine V. Way, Michael |
author_sort | Barry, David J. |
collection | PubMed |
description | Cell migration is frequently accompanied by changes in cell morphology (morphodynamics) on a range of spatial and temporal scales. Despite recent advances in imaging techniques, the application of unbiased computational image analysis methods for morphodynamic quantification is rare. For example, manual analysis using kymographs is still commonplace, often caused by lack of access to user-friendly, automated tools. We now describe software designed for the automated quantification of cell migration and morphodynamics. Implemented as a plug-in for the open-source platform, ImageJ, ADAPT is capable of rapid, automated analysis of migration and membrane protrusions, together with associated fluorescently labeled proteins, across multiple cells. We demonstrate the ability of the software by quantifying variations in cell population migration rates on different extracellular matrices. We also show that ADAPT can detect and morphologically profile filopodia. Finally, we have used ADAPT to compile an unbiased description of a “typical” bleb formed at the plasma membrane and quantify the effect of Arp2/3 complex inhibition on bleb retraction. |
format | Online Article Text |
id | pubmed-4395480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43954802015-10-13 Open source software for quantification of cell migration, protrusions, and fluorescence intensities Barry, David J. Durkin, Charlotte H. Abella, Jasmine V. Way, Michael J Cell Biol Research Articles Cell migration is frequently accompanied by changes in cell morphology (morphodynamics) on a range of spatial and temporal scales. Despite recent advances in imaging techniques, the application of unbiased computational image analysis methods for morphodynamic quantification is rare. For example, manual analysis using kymographs is still commonplace, often caused by lack of access to user-friendly, automated tools. We now describe software designed for the automated quantification of cell migration and morphodynamics. Implemented as a plug-in for the open-source platform, ImageJ, ADAPT is capable of rapid, automated analysis of migration and membrane protrusions, together with associated fluorescently labeled proteins, across multiple cells. We demonstrate the ability of the software by quantifying variations in cell population migration rates on different extracellular matrices. We also show that ADAPT can detect and morphologically profile filopodia. Finally, we have used ADAPT to compile an unbiased description of a “typical” bleb formed at the plasma membrane and quantify the effect of Arp2/3 complex inhibition on bleb retraction. The Rockefeller University Press 2015-04-13 /pmc/articles/PMC4395480/ /pubmed/25847537 http://dx.doi.org/10.1083/jcb.201501081 Text en © 2015 Barry et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Barry, David J. Durkin, Charlotte H. Abella, Jasmine V. Way, Michael Open source software for quantification of cell migration, protrusions, and fluorescence intensities |
title | Open source software for quantification of cell migration, protrusions, and fluorescence intensities |
title_full | Open source software for quantification of cell migration, protrusions, and fluorescence intensities |
title_fullStr | Open source software for quantification of cell migration, protrusions, and fluorescence intensities |
title_full_unstemmed | Open source software for quantification of cell migration, protrusions, and fluorescence intensities |
title_short | Open source software for quantification of cell migration, protrusions, and fluorescence intensities |
title_sort | open source software for quantification of cell migration, protrusions, and fluorescence intensities |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4395480/ https://www.ncbi.nlm.nih.gov/pubmed/25847537 http://dx.doi.org/10.1083/jcb.201501081 |
work_keys_str_mv | AT barrydavidj opensourcesoftwareforquantificationofcellmigrationprotrusionsandfluorescenceintensities AT durkincharlotteh opensourcesoftwareforquantificationofcellmigrationprotrusionsandfluorescenceintensities AT abellajasminev opensourcesoftwareforquantificationofcellmigrationprotrusionsandfluorescenceintensities AT waymichael opensourcesoftwareforquantificationofcellmigrationprotrusionsandfluorescenceintensities |