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Directing cell migration and organization via nanocrater-patterned cell-repellent interfaces

Although adhesive interactions between cells and nanostructured interfaces have been studied extensively(1–6), there is a paucity of data on how nanostructured interfaces repel cells by directing cell migration and cell-colony organization. Here, by using multiphoton ablation lithography(7) to patte...

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Autores principales: Jeon, Hojeong, Koo, Sangmo, Reese, Willie Mae, Loskill, Peter, Grigoropoulos, Costas P., Healy, Kevin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545687/
https://www.ncbi.nlm.nih.gov/pubmed/26213899
http://dx.doi.org/10.1038/nmat4342
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author Jeon, Hojeong
Koo, Sangmo
Reese, Willie Mae
Loskill, Peter
Grigoropoulos, Costas P.
Healy, Kevin E.
author_facet Jeon, Hojeong
Koo, Sangmo
Reese, Willie Mae
Loskill, Peter
Grigoropoulos, Costas P.
Healy, Kevin E.
author_sort Jeon, Hojeong
collection PubMed
description Although adhesive interactions between cells and nanostructured interfaces have been studied extensively(1–6), there is a paucity of data on how nanostructured interfaces repel cells by directing cell migration and cell-colony organization. Here, by using multiphoton ablation lithography(7) to pattern surfaces with nanoscale craters of various aspect ratios and pitches, we show that the surfaces altered the cells’ focal-adhesion size and distribution, thus affecting cell morphology, migration and ultimately localization. We also show that nanocrater pitch can disrupt the formation of mature focal adhesions to favour the migration of cells toward higher-pitched regions, which present increased planar area for the formation of stable focal adhesions. Moreover, by designing surfaces with variable pitch but constant nanocrater dimensions, we were able to create circular and striped cellular patterns. Our surface-patterning approach, which does not involve chemical treatments and can be applied to various materials, represents a simple method to control cell behaviour on surfaces.
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spelling pubmed-45456872016-03-01 Directing cell migration and organization via nanocrater-patterned cell-repellent interfaces Jeon, Hojeong Koo, Sangmo Reese, Willie Mae Loskill, Peter Grigoropoulos, Costas P. Healy, Kevin E. Nat Mater Article Although adhesive interactions between cells and nanostructured interfaces have been studied extensively(1–6), there is a paucity of data on how nanostructured interfaces repel cells by directing cell migration and cell-colony organization. Here, by using multiphoton ablation lithography(7) to pattern surfaces with nanoscale craters of various aspect ratios and pitches, we show that the surfaces altered the cells’ focal-adhesion size and distribution, thus affecting cell morphology, migration and ultimately localization. We also show that nanocrater pitch can disrupt the formation of mature focal adhesions to favour the migration of cells toward higher-pitched regions, which present increased planar area for the formation of stable focal adhesions. Moreover, by designing surfaces with variable pitch but constant nanocrater dimensions, we were able to create circular and striped cellular patterns. Our surface-patterning approach, which does not involve chemical treatments and can be applied to various materials, represents a simple method to control cell behaviour on surfaces. 2015-07-27 2015-09 /pmc/articles/PMC4545687/ /pubmed/26213899 http://dx.doi.org/10.1038/nmat4342 Text en Reprints and permissions information is available online at www.nature.com/reprints.
spellingShingle Article
Jeon, Hojeong
Koo, Sangmo
Reese, Willie Mae
Loskill, Peter
Grigoropoulos, Costas P.
Healy, Kevin E.
Directing cell migration and organization via nanocrater-patterned cell-repellent interfaces
title Directing cell migration and organization via nanocrater-patterned cell-repellent interfaces
title_full Directing cell migration and organization via nanocrater-patterned cell-repellent interfaces
title_fullStr Directing cell migration and organization via nanocrater-patterned cell-repellent interfaces
title_full_unstemmed Directing cell migration and organization via nanocrater-patterned cell-repellent interfaces
title_short Directing cell migration and organization via nanocrater-patterned cell-repellent interfaces
title_sort directing cell migration and organization via nanocrater-patterned cell-repellent interfaces
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545687/
https://www.ncbi.nlm.nih.gov/pubmed/26213899
http://dx.doi.org/10.1038/nmat4342
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