Dynamic cell adhesion and migration on nanoscale grooved substrates

Organised nanotopography mimicking the natural extracellular matrix can be used to control morphology, cell motility, and differentiation. However, it is still unknown how specific cell types react with specific patterns. Both initial adhesion and preferential cell migration may be important to init...

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Main Authors: E Lamers, J te Riet, M Domanski, R Luttge, CG Figdor, JGE Gardeniers, XF Walboomers, JA Jansen
Format: Article
Language:English
Published: AO Research Institute Davos 2012-03-01
Series:European Cells & Materials
Subjects:
Online Access:http://www.ecmjournal.org/journal/papers/vol023/pdf/v023a14.pdf
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spelling doaj-e5c3c249908942ed920c464f9244d5af2020-11-24T22:26:45Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622012-03-0123182194Dynamic cell adhesion and migration on nanoscale grooved substratesE LamersJ te RietM DomanskiR LuttgeCG FigdorJGE GardeniersXF WalboomersJA JansenOrganised nanotopography mimicking the natural extracellular matrix can be used to control morphology, cell motility, and differentiation. However, it is still unknown how specific cell types react with specific patterns. Both initial adhesion and preferential cell migration may be important to initiate and increase cell locomotion and coverage with cells, and thus achieve an enhanced wound healing response around an implantable material. Therefore, the aim of this study was to evaluate how MC3T3-E1 osteoblast initial adhesion and directional migration are influenced by nanogrooves with pitches ranging from 150 nm up to 1000 nm. In this study, we used a multi-patterned substrate with five different groove patterns and a smooth area with either a concentric or radial orientation. Initial cell adhesion measurements after 10 s were performed using atomic force spectroscopy-assisted single-cell force spectroscopy, and demonstrated that nascent cell adhesion was highly induced by a 600 nm pitch and reduced by a 150 nm pitch. Addition of RGD peptide significantly reduced adhesion, indicating that integrins and cell adhesive proteins (e.g. fibronectin or vitronectin) are key factors in specific cell adhesion on nanogrooved substrates. Also, cell migration was highly dependent on the groove pitch; the highest directional migration parallel to the grooves was observed on a 600 nm pitch, whereas a 150 nm pitch restrained directional cell migration. From this study, we conclude that grooves with a pitch of 600 nm may be favourable to enhance fast wound closure, thereby promoting tissue regeneration.http://www.ecmjournal.org/journal/papers/vol023/pdf/v023a14.pdfCell-protein-material interactionstissue-material interactionsbiomaterialsnanotechnologyimagingAFM profilometrycells motilitycell migrationtissue adhesion
collection DOAJ
language English
format Article
sources DOAJ
author E Lamers
J te Riet
M Domanski
R Luttge
CG Figdor
JGE Gardeniers
XF Walboomers
JA Jansen
spellingShingle E Lamers
J te Riet
M Domanski
R Luttge
CG Figdor
JGE Gardeniers
XF Walboomers
JA Jansen
Dynamic cell adhesion and migration on nanoscale grooved substrates
European Cells & Materials
Cell-protein-material interactions
tissue-material interactions
biomaterials
nanotechnology
imaging
AFM profilometry
cells motility
cell migration
tissue adhesion
author_facet E Lamers
J te Riet
M Domanski
R Luttge
CG Figdor
JGE Gardeniers
XF Walboomers
JA Jansen
author_sort E Lamers
title Dynamic cell adhesion and migration on nanoscale grooved substrates
title_short Dynamic cell adhesion and migration on nanoscale grooved substrates
title_full Dynamic cell adhesion and migration on nanoscale grooved substrates
title_fullStr Dynamic cell adhesion and migration on nanoscale grooved substrates
title_full_unstemmed Dynamic cell adhesion and migration on nanoscale grooved substrates
title_sort dynamic cell adhesion and migration on nanoscale grooved substrates
publisher AO Research Institute Davos
series European Cells & Materials
issn 1473-2262
publishDate 2012-03-01
description Organised nanotopography mimicking the natural extracellular matrix can be used to control morphology, cell motility, and differentiation. However, it is still unknown how specific cell types react with specific patterns. Both initial adhesion and preferential cell migration may be important to initiate and increase cell locomotion and coverage with cells, and thus achieve an enhanced wound healing response around an implantable material. Therefore, the aim of this study was to evaluate how MC3T3-E1 osteoblast initial adhesion and directional migration are influenced by nanogrooves with pitches ranging from 150 nm up to 1000 nm. In this study, we used a multi-patterned substrate with five different groove patterns and a smooth area with either a concentric or radial orientation. Initial cell adhesion measurements after 10 s were performed using atomic force spectroscopy-assisted single-cell force spectroscopy, and demonstrated that nascent cell adhesion was highly induced by a 600 nm pitch and reduced by a 150 nm pitch. Addition of RGD peptide significantly reduced adhesion, indicating that integrins and cell adhesive proteins (e.g. fibronectin or vitronectin) are key factors in specific cell adhesion on nanogrooved substrates. Also, cell migration was highly dependent on the groove pitch; the highest directional migration parallel to the grooves was observed on a 600 nm pitch, whereas a 150 nm pitch restrained directional cell migration. From this study, we conclude that grooves with a pitch of 600 nm may be favourable to enhance fast wound closure, thereby promoting tissue regeneration.
topic Cell-protein-material interactions
tissue-material interactions
biomaterials
nanotechnology
imaging
AFM profilometry
cells motility
cell migration
tissue adhesion
url http://www.ecmjournal.org/journal/papers/vol023/pdf/v023a14.pdf
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AT jteriet dynamiccelladhesionandmigrationonnanoscalegroovedsubstrates
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