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dc.contributor.authorBeckwith, Kai Sandvold
dc.contributor.authorUllmann, Sindre
dc.contributor.authorVinje, Jakob
dc.contributor.authorSikorski, Pawel
dc.date.accessioned2020-01-14T08:57:47Z
dc.date.available2020-01-14T08:57:47Z
dc.date.created2019-09-17T13:38:13Z
dc.date.issued2019
dc.identifier.citationSmall. 2019, 15 (43), 1902514-?.nb_NO
dc.identifier.issn1613-6810
dc.identifier.urihttp://hdl.handle.net/11250/2636099
dc.description.abstractSurfaces decorated with high aspect ratio nanostructures are a promising tool to study cellular processes and design novel devices to control cellular behavior. However, little is known about the dynamics of cellular phenomenon such as adhesion, spreading, and migration on such surfaces. In particular, how these are influenced by the surface properties. In this work, fibroblast behavior is investigated on regular arrays of 1 µm high polymer nanopillars with varying pillar to pillar distance. Embryonic mouse fibroblasts (NIH‐3T3) spread on all arrays, and on contact with the substrate engulf nanopillars independently of the array pitch. As the cells start to spread, different behavior is observed. On dense arrays which have a pitch equal or below 1 µm, cells are suspended on top of the nanopillars, making only sporadic contact with the glass support. Cells stay attached to the glass support and fully engulf nanopillars during spreading and migration on the sparse arrays which have a pitch of 2 µm and above. These alternate states have a profound effect on cell migration rates. Dynamic F‐actin puncta colocalize with nanopillars during cell spreading and migration. Strong membrane association with engulfed nanopillars might explain the reduced migration rates on sparse arrays.nb_NO
dc.language.isoengnb_NO
dc.publisherWileynb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleInfluence of Nanopillar Arrays on Fibroblast Motility, Adhesion, and Migration Mechanismsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1902514-?nb_NO
dc.source.volume15nb_NO
dc.source.journalSmallnb_NO
dc.source.issue43nb_NO
dc.identifier.doi10.1002/smll.201902514
dc.identifier.cristin1725687
dc.relation.projectNorges forskningsråd: 223255nb_NO
dc.relation.projectNorges forskningsråd: 245963nb_NO
dc.description.localcode© 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly citednb_NO
cristin.unitcode194,65,15,0
cristin.unitcode194,66,20,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameInstitutt for fysikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal