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@ARTICLE{Blaschke:861214,
author = {Blaschke, Stefan and Vay, Sabine Ulrike and Pallast, Niklas
and Rabenstein, Monika and Abraham, Jella-Andrea and
Linnartz, Christina and Hoffmann, Marco and Hersch, Nils and
Merkel, Rudolf and Hoffmann, Bernd and Fink, Gereon Rudolf
and Rueger, Maria Adele},
title = {{S}ubstrate elasticity induces quiescence and promotes
neurogenesis of primary neural stem cells - a biophysical in
vitro model of the physiological cerebral milieu},
journal = {Journal of tissue engineering and regenerative medicine},
volume = {13},
number = {6},
issn = {1932-6254},
address = {Hoboken, NJ [u.a.]},
publisher = {Wiley},
reportid = {FZJ-2019-01735},
pages = {960-972},
year = {2019},
abstract = {In the brain, neural stem cells (NSC) are tightly regulated
by external signals and biophysical cues mediated by the
local microenvironment or “niche.” In particular, the
influence of tissue elasticity, known to fundamentally
affect the function of various cell types in the body, on
NSC remains poorly understood. We, accordingly, aimed to
characterize the effects of elastic substrates on critical
NSC functions. Primary rat NSC were grown as monolayers on
polydimethylsiloxane‐ (PDMS‐) based gels. PDMS‐coated
cell culture plates, simulating the physiological
microenvironment of the living brain, were generated in
various degrees of elasticity, ranging from 1 to 50 kPa;
additionally, results were compared with regular glass
plates as usually used in cell culture work. Survival of NSC
on the PDMS‐based substrates was unimpaired. The
proliferation rate on 1 kPa PDMS decreased by $45\%$
compared with stiffer PMDS substrates of 50 kPa (p < 0.05)
whereas expression of cyclin‐dependent kinase inhibitor
1B/p27Kip1 increased more than two fold (p < 0.01),
suggesting NSC quiescence. NSC differentiation was
accelerated on softer substrates and favored the generation
of neurons $(42\%$ neurons on 1 kPa PDMS vs. $25\%$ on 50
kPa PDMS; p < 0.05). Neurons generated on 1 kPa PDMS showed
$29\%$ longer neurites compared with those on stiffer PDMS
substrates (p < 0.05), suggesting optimized neuronal
maturation and an accelerated generation of neuronal
networks. Data show that primary NSC are significantly
affected by the mechanical properties of their
microenvironment. Culturing NSC on a substrate of
brain‐like elasticity keeps them in their physiological,
quiescent state and increases their neurogenic potential.},
cin = {INM-3 / ICS-7},
ddc = {610},
cid = {I:(DE-Juel1)INM-3-20090406 / I:(DE-Juel1)ICS-7-20110106},
pnm = {572 - (Dys-)function and Plasticity (POF3-572)},
pid = {G:(DE-HGF)POF3-572},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30815982},
UT = {WOS:000473660800005},
doi = {10.1002/term.2838},
url = {https://juser.fz-juelich.de/record/861214},
}