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@INPROCEEDINGS{Rinklin:141739,
author = {Rinklin, Philipp and Afanasenkau, Dzmitry and Wiegand,
Simone and Wolfrum, Bernhard},
title = {{M}icrowire crossbar arrays for on-chip localized thermal
lesion of cell cultures},
reportid = {FZJ-2014-00105},
year = {2013},
abstract = {Driven by an advance in microfabrication technologies, the
development of miniaturized analytical platforms has become
a major interest in physical, chemical, and biological
research over the past two decades. On one hand, these
systems offer the possibility to massively decrease the
amount of resources and time necessary for current
point-of-care medical diagnostics. On the other hand, the
possibility to interact with biological systems in a highly
controlled and easily parallelizable manner offers many
promising opportunities for fundamental biological and
biophysical research. For example, when studying the healing
process of complex tissues after lesion, the use of
simplified in vitro models can help to elucidate basic
mechanisms. In this context, a means to create these lesions
with high spatial control and resolution is of great
importance. While the use of lasers coupled to microscopes
is capable of delivering the necessary control and
resolution, the requirement of external optics renders an
application to on-chip devices difficult. Here, we
demonstrate the use of microwire crossbar chips for the
generation of localized thermally induced lesions in on-chip
tissue models. Our chips consist of two orthogonal layers of
parallel microwires, insulated from the culture medium by a
polyimide layer. Cardiomyocyte-like HL-1 cells are cultured
on the chip as an in vitro tissue model. Passing an
electrical current through a given set of microwires leads
to thermal heating of the active wires, which consequently
imposes a localized stress on the cells cultured at the
chip’s surface. We demonstrate that using this method,
complex lesion patterns with a resolution in the lower
micrometer regime can be created. The success of the lesion
as well as the effects on the surrounding cells are
evaluated using Calcein/EtHD staining methods. We further
analyze the distinct Ca2+ propagation inside the cell layer
revealing partially decoupled network activity depending on
the applied lesion patterns. In conclusion, we believe that
our method can be used as a versatile tool to study tissue
lesions in simplified model systems. As a chip-based method,
it also allows for low-cost production, as well as
straight-forward inclusion in microsystems, which
facilitates high-throughput and the generation of
statistically relevant data from biological systems prone to
high noise levels.},
month = {Nov},
date = {2013-11-18},
organization = {NanoBioTech Montreux, Montreux
(Switzerland), 18 Nov 2013 - 20 Nov
2013},
subtyp = {After Call},
cin = {PGI-8 / ICS-8 / JARA-FIT / ICS-3},
cid = {I:(DE-Juel1)PGI-8-20110106 / I:(DE-Juel1)ICS-8-20110106 /
I:(DE-Juel1)VDB881 / I:(DE-Juel1)ICS-3-20110106},
pnm = {453 - Physics of the Cell (POF2-453) / 423 - Sensorics and
bioinspired systems (POF2-423) / 452 - Structural Biology
(POF2-452)},
pid = {G:(DE-HGF)POF2-453 / G:(DE-HGF)POF2-423 /
G:(DE-HGF)POF2-452},
typ = {PUB:(DE-HGF)24},
url = {https://juser.fz-juelich.de/record/141739},
}