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One-dimensional topography underlies three-dimensional fibrillar cell migration

Current concepts of cell migration were established in regular two-dimensional (2D) cell culture, but the roles of topography are poorly understood for cells migrating in an oriented 3D fibrillar extracellular matrix (ECM). We use a novel micropatterning technique termed microphotopatterning (μPP) t...

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Detalles Bibliográficos
Autores principales: Doyle, Andrew D., Wang, Francis W., Matsumoto, Kazue, Yamada, Kenneth M.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654121/
https://www.ncbi.nlm.nih.gov/pubmed/19221195
http://dx.doi.org/10.1083/jcb.200810041
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author Doyle, Andrew D.
Wang, Francis W.
Matsumoto, Kazue
Yamada, Kenneth M.
author_facet Doyle, Andrew D.
Wang, Francis W.
Matsumoto, Kazue
Yamada, Kenneth M.
author_sort Doyle, Andrew D.
collection PubMed
description Current concepts of cell migration were established in regular two-dimensional (2D) cell culture, but the roles of topography are poorly understood for cells migrating in an oriented 3D fibrillar extracellular matrix (ECM). We use a novel micropatterning technique termed microphotopatterning (μPP) to identify functions for 1D fibrillar patterns in 3D cell migration. In striking contrast to 2D, cell migration in both 1D and 3D is rapid, uniaxial, independent of ECM ligand density, and dependent on myosin II contractility and microtubules (MTs). 1D and 3D migration are also characterized by an anterior MT bundle with a posterior centrosome. We propose that cells migrate rapidly through 3D fibrillar matrices by a 1D migratory mechanism not mimicked by 2D matrices.
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spelling pubmed-26541212009-08-23 One-dimensional topography underlies three-dimensional fibrillar cell migration Doyle, Andrew D. Wang, Francis W. Matsumoto, Kazue Yamada, Kenneth M. J Cell Biol Research Articles Current concepts of cell migration were established in regular two-dimensional (2D) cell culture, but the roles of topography are poorly understood for cells migrating in an oriented 3D fibrillar extracellular matrix (ECM). We use a novel micropatterning technique termed microphotopatterning (μPP) to identify functions for 1D fibrillar patterns in 3D cell migration. In striking contrast to 2D, cell migration in both 1D and 3D is rapid, uniaxial, independent of ECM ligand density, and dependent on myosin II contractility and microtubules (MTs). 1D and 3D migration are also characterized by an anterior MT bundle with a posterior centrosome. We propose that cells migrate rapidly through 3D fibrillar matrices by a 1D migratory mechanism not mimicked by 2D matrices. The Rockefeller University Press 2009-02-23 /pmc/articles/PMC2654121/ /pubmed/19221195 http://dx.doi.org/10.1083/jcb.200810041 Text en 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.jcb.org/misc/terms.shtml). 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
Doyle, Andrew D.
Wang, Francis W.
Matsumoto, Kazue
Yamada, Kenneth M.
One-dimensional topography underlies three-dimensional fibrillar cell migration
title One-dimensional topography underlies three-dimensional fibrillar cell migration
title_full One-dimensional topography underlies three-dimensional fibrillar cell migration
title_fullStr One-dimensional topography underlies three-dimensional fibrillar cell migration
title_full_unstemmed One-dimensional topography underlies three-dimensional fibrillar cell migration
title_short One-dimensional topography underlies three-dimensional fibrillar cell migration
title_sort one-dimensional topography underlies three-dimensional fibrillar cell migration
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654121/
https://www.ncbi.nlm.nih.gov/pubmed/19221195
http://dx.doi.org/10.1083/jcb.200810041
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