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@ARTICLE{Abagnale:200940,
author = {Abagnale, Giulio and Steger, Michael and Nguyen, Vu Hoa and
Hersch, Nils and Sechi, Antonio and Joussen, Sylvia and
Denecke, Bernd and Merkel, Rudolf and Hoffmann, Bernd and
Dreser, Alice and Schnakenberg, Uwe and Gillner, Arnold and
Wagner, Wolfgang},
title = {{S}urface topography enhances differentiation of
mesenchymal stem cells towards osteogenic and adipogenic
lineages},
journal = {Biomaterials},
volume = {61},
issn = {0142-9612},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {FZJ-2015-03281},
pages = {316 - 326},
year = {2015},
abstract = {Surface topography impacts on cell growth and
differentiation, but it is not trivial to generate defined
surface structures and to assess the relevance of specific
topographic parameters. In this study, we have
systematically compared in vitro differentiation of
mesenchymal stem cells (MSCs) on a variety of groove/ridge
structures. Micro- and nano-patterns were generated in
polyimide using reactive ion etching or multi beam laser
interference, respectively. These structures affected cell
spreading and orientation of human MSCs, which was also
reflected in focal adhesions morphology and size. Time-lapse
demonstrated directed migration parallel to the
nano-patterns. Overall, surface patterns clearly enhanced
differentiation of MSCs towards specific lineages: 15 μm
ridges increased adipogenic differentiation whereas 2 μm
ridges enhanced osteogenic differentiation. Notably,
nano-patterns with a periodicity of 650 nm increased
differentiation towards both osteogenic and adipogenic
lineages. However, in absence of differentiation media
surface structures did neither induce differentiation, nor
lineage-specific gene expression changes. Furthermore,
nanostructures did not affect the YAP/TAZ complex, which is
activated by substrate stiffness. Our results provide
further insight into how structuring of tailored
biomaterials and implant interfaces – e.g. by multi beam
laser interference in sub-micrometer scale – do not induce
differentiation of MSCs per se, but support their directed
differentiation.},
cin = {ICS-7},
ddc = {570},
cid = {I:(DE-Juel1)ICS-7-20110106},
pnm = {552 - Engineering Cell Function (POF3-552)},
pid = {G:(DE-HGF)POF3-552},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000357229900030},
pubmed = {pmid:26026844},
doi = {10.1016/j.biomaterials.2015.05.030},
url = {https://juser.fz-juelich.de/record/200940},
}