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In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis
Cell migration is a key procedure involved in many biological processes including embryological development, tissue formation, immune defense or inflammation, and cancer progression. How physical, chemical, and molecular aspects can affect cell motility is a challenge to understand migratory cells b...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587234/ https://www.ncbi.nlm.nih.gov/pubmed/31259172 http://dx.doi.org/10.3389/fcell.2019.00107 |
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author | Pijuan, Jordi Barceló, Carla Moreno, David F. Maiques, Oscar Sisó, Pol Marti, Rosa M. Macià, Anna Panosa, Anaïs |
author_facet | Pijuan, Jordi Barceló, Carla Moreno, David F. Maiques, Oscar Sisó, Pol Marti, Rosa M. Macià, Anna Panosa, Anaïs |
author_sort | Pijuan, Jordi |
collection | PubMed |
description | Cell migration is a key procedure involved in many biological processes including embryological development, tissue formation, immune defense or inflammation, and cancer progression. How physical, chemical, and molecular aspects can affect cell motility is a challenge to understand migratory cells behavior. In vitro assays are excellent approaches to extrapolate to in vivo situations and study live cells behavior. Here we present four in vitro protocols that describe step-by-step cell migration, invasion and adhesion strategies and their corresponding image data quantification. These current protocols are based on two-dimensional wound healing assays (comparing traditional pipette tip-scratch assay vs. culture insert assay), 2D individual cell-tracking experiments by live cell imaging and three-dimensional spreading and transwell assays. All together, they cover different phenotypes and hallmarks of cell motility and adhesion, providing orthogonal information that can be used either individually or collectively in many different experimental setups. These optimized protocols will facilitate physiological and cellular characterization of these processes, which may be used for fast screening of specific therapeutic cancer drugs for migratory function, novel strategies in cancer diagnosis, and for assaying new molecules involved in adhesion and invasion metastatic properties of cancer cells. |
format | Online Article Text |
id | pubmed-6587234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65872342019-06-28 In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis Pijuan, Jordi Barceló, Carla Moreno, David F. Maiques, Oscar Sisó, Pol Marti, Rosa M. Macià, Anna Panosa, Anaïs Front Cell Dev Biol Cell and Developmental Biology Cell migration is a key procedure involved in many biological processes including embryological development, tissue formation, immune defense or inflammation, and cancer progression. How physical, chemical, and molecular aspects can affect cell motility is a challenge to understand migratory cells behavior. In vitro assays are excellent approaches to extrapolate to in vivo situations and study live cells behavior. Here we present four in vitro protocols that describe step-by-step cell migration, invasion and adhesion strategies and their corresponding image data quantification. These current protocols are based on two-dimensional wound healing assays (comparing traditional pipette tip-scratch assay vs. culture insert assay), 2D individual cell-tracking experiments by live cell imaging and three-dimensional spreading and transwell assays. All together, they cover different phenotypes and hallmarks of cell motility and adhesion, providing orthogonal information that can be used either individually or collectively in many different experimental setups. These optimized protocols will facilitate physiological and cellular characterization of these processes, which may be used for fast screening of specific therapeutic cancer drugs for migratory function, novel strategies in cancer diagnosis, and for assaying new molecules involved in adhesion and invasion metastatic properties of cancer cells. Frontiers Media S.A. 2019-06-14 /pmc/articles/PMC6587234/ /pubmed/31259172 http://dx.doi.org/10.3389/fcell.2019.00107 Text en Copyright © 2019 Pijuan, Barceló, Moreno, Maiques, Sisó, Marti, Macià and Panosa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Pijuan, Jordi Barceló, Carla Moreno, David F. Maiques, Oscar Sisó, Pol Marti, Rosa M. Macià, Anna Panosa, Anaïs In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis |
title | In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis |
title_full | In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis |
title_fullStr | In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis |
title_full_unstemmed | In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis |
title_short | In vitro Cell Migration, Invasion, and Adhesion Assays: From Cell Imaging to Data Analysis |
title_sort | in vitro cell migration, invasion, and adhesion assays: from cell imaging to data analysis |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587234/ https://www.ncbi.nlm.nih.gov/pubmed/31259172 http://dx.doi.org/10.3389/fcell.2019.00107 |
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