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An adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces

Collective cell migration is critical for proper embryonic development, wound healing, and cancer cell invasion. However, much of our knowledge of cell migration has been performed using flat surfaces that lack topographical features and do not recapitulate the complex fibrous architecture of the ex...

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Autores principales: Loesel, Kristen E., Hiraki, Harrison L., Baker, Brendon M., Parent, Carole A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9909417/
https://www.ncbi.nlm.nih.gov/pubmed/36776562
http://dx.doi.org/10.3389/fcell.2023.1106653
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author Loesel, Kristen E.
Hiraki, Harrison L.
Baker, Brendon M.
Parent, Carole A.
author_facet Loesel, Kristen E.
Hiraki, Harrison L.
Baker, Brendon M.
Parent, Carole A.
author_sort Loesel, Kristen E.
collection PubMed
description Collective cell migration is critical for proper embryonic development, wound healing, and cancer cell invasion. However, much of our knowledge of cell migration has been performed using flat surfaces that lack topographical features and do not recapitulate the complex fibrous architecture of the extracellular matrix (ECM). The recent availability of synthetic fibrous networks designed to mimic in vivo ECM has been key to identify the topological features that dictate cell migration patterns as well as to determine the underlying mechanisms that regulate topography-sensing. Recent studies have underscored the prevalence of collective cell migration during cancer invasion, and these observations present a compelling need to understand the mechanisms controlling contact guidance within migratory, multicellular groups. Therefore, we designed an integrated migration analysis platform combining tunable electrospun fibers that recapitulate aspects of the biophysical properties of the ECM, and computational approaches to investigate collective cell migration. To quantitatively assess migration as a function of matrix topography, we developed an automated MATLAB code that quantifies cell migration dynamics, including speed, directionality, and the number of detached cells. This platform enables live cell imaging while providing enough cells for biochemical, proteomic, and genomic analyses, making our system highly adaptable to multiple experimental investigations.
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spelling pubmed-99094172023-02-10 An adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces Loesel, Kristen E. Hiraki, Harrison L. Baker, Brendon M. Parent, Carole A. Front Cell Dev Biol Cell and Developmental Biology Collective cell migration is critical for proper embryonic development, wound healing, and cancer cell invasion. However, much of our knowledge of cell migration has been performed using flat surfaces that lack topographical features and do not recapitulate the complex fibrous architecture of the extracellular matrix (ECM). The recent availability of synthetic fibrous networks designed to mimic in vivo ECM has been key to identify the topological features that dictate cell migration patterns as well as to determine the underlying mechanisms that regulate topography-sensing. Recent studies have underscored the prevalence of collective cell migration during cancer invasion, and these observations present a compelling need to understand the mechanisms controlling contact guidance within migratory, multicellular groups. Therefore, we designed an integrated migration analysis platform combining tunable electrospun fibers that recapitulate aspects of the biophysical properties of the ECM, and computational approaches to investigate collective cell migration. To quantitatively assess migration as a function of matrix topography, we developed an automated MATLAB code that quantifies cell migration dynamics, including speed, directionality, and the number of detached cells. This platform enables live cell imaging while providing enough cells for biochemical, proteomic, and genomic analyses, making our system highly adaptable to multiple experimental investigations. Frontiers Media S.A. 2023-01-26 /pmc/articles/PMC9909417/ /pubmed/36776562 http://dx.doi.org/10.3389/fcell.2023.1106653 Text en Copyright © 2023 Loesel, Hiraki, Baker and Parent. https://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
Loesel, Kristen E.
Hiraki, Harrison L.
Baker, Brendon M.
Parent, Carole A.
An adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces
title An adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces
title_full An adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces
title_fullStr An adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces
title_full_unstemmed An adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces
title_short An adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces
title_sort adaptive and versatile method to quantitate and characterize collective cell migration behaviors on complex surfaces
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9909417/
https://www.ncbi.nlm.nih.gov/pubmed/36776562
http://dx.doi.org/10.3389/fcell.2023.1106653
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