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Morphological and microarray analysis of human fibroblasts cultured on nanocolumns produced by colloidal lithography.
Dalby, M J; Riehle, M O; Sutherland, D S; Agheli, H; Curtis, A S G.
Affiliation
  • Dalby MJ; Centre for Cell Engineering, Institute of Biomedical and Life Sciences, Joseph Black Building, University of Glasgow, Glasgow, G12 8QQ, UK. m.dalby@bio.gla.ac.uk
Eur Cell Mater ; 9: 1-8; discussion 8, 2005 Jan 13.
Article in En | MEDLINE | ID: mdl-15690263
ABSTRACT
The environment around a cell during in vitro culture is unlikely to mimic those in vivo. Preliminary experiments with nanotopography have shown that nanoscale features can strongly influence cell morphology, adhesion, proliferation and gene regulation, but the mechanisms mediating this cell response remain unclear. In this study a well defined nanotopography, consisting of 100 nm wide and 160 nm high cylindrical columns, was used in fibroblast culture. In order to build on previously published morphological data that showed changes in cell spreading on the nanocolumns, in this study gene regulation was monitored using a 1718 gene microarray. Transmission electron microscopy, fluorescent observation of actin and Rac and area quantification have been used to re-affirm the microarray observations. The results indicate that changes in cell spreading correlate with a number of gene up- and down-regulations as will be described within the manuscript.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Colloids / Nanotechnology / Microarray Analysis / Fibroblasts Limits: Animals / Humans Language: En Journal: Eur Cell Mater Year: 2005 Document type: Article Affiliation country: United kingdom
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Colloids / Nanotechnology / Microarray Analysis / Fibroblasts Limits: Animals / Humans Language: En Journal: Eur Cell Mater Year: 2005 Document type: Article Affiliation country: United kingdom