Microscaffolds by Direct Laser Writing for Neurite Guidance Leading to Tailor-Made Neuronal Networks

Standard

Microscaffolds by Direct Laser Writing for Neurite Guidance Leading to Tailor-Made Neuronal Networks. / Fendler, Cornelius; Denker, Christian ; Harberts , Jann ; Bayat, Parisa; Zierold, Robert ; Loers, Gabriele; Münzenberg , Markus ; Blick, Robert H.

in: ADV BIOSYST, Jahrgang 3, Nr. 5, 05.2019, S. e1800329.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Fendler, C, Denker, C, Harberts , J, Bayat, P, Zierold, R, Loers, G, Münzenberg , M & Blick, RH 2019, 'Microscaffolds by Direct Laser Writing for Neurite Guidance Leading to Tailor-Made Neuronal Networks', ADV BIOSYST, Jg. 3, Nr. 5, S. e1800329.

APA

Fendler, C., Denker, C., Harberts , J., Bayat, P., Zierold, R., Loers, G., Münzenberg , M., & Blick, R. H. (2019). Microscaffolds by Direct Laser Writing for Neurite Guidance Leading to Tailor-Made Neuronal Networks. ADV BIOSYST, 3(5), e1800329.

Vancouver

Fendler C, Denker C, Harberts J, Bayat P, Zierold R, Loers G et al. Microscaffolds by Direct Laser Writing for Neurite Guidance Leading to Tailor-Made Neuronal Networks. ADV BIOSYST. 2019 Mai;3(5):e1800329.

Bibtex

@article{7cae3a93e69c4cb89c7e5398fd7e82f3,
title = "Microscaffolds by Direct Laser Writing for Neurite Guidance Leading to Tailor-Made Neuronal Networks",
abstract = "While modern day integrated electronic circuits are essentially designed in a 2D fashion, the brain can be regarded as a 3D circuit. The thus enhanced connectivity enables much more complex signal processing as compared to conventional 2D circuits. Recent technological advances in the development of nano/microscale 3D structuring have led to the development of artificial neuron culturing platforms, which surpass the possibilities of classical 2D cultures. In this work, in vitro culturing of neuronal networks is demonstrated by determining predefined pathways through topological and chemical neurite guiding. Tailor-made culturing substrates of microtowers and freestanding microtubes are fabricated using direct laser writing by two-photon polymerization. The first scaffold design that allows for site-specific cell attachment and directed outgrowth of single neurites along defined paths that can be arranged freely in all dimensions, to build neuronal networks with low cell density, is presented. The neurons cultured in the scaffolds show characteristic electrophysiological properties of vital cells after 10 d in vitro. The introduced scaffold design offers a promising concept for future complex neuronal network studies on defined neuronal circuits with tailor-made design specific neurite connections beyond 2D. ",
author = "Cornelius Fendler and Christian Denker and Jann Harberts and Parisa Bayat and Robert Zierold and Gabriele Loers and Markus M{\"u}nzenberg and Blick, {Robert H}",
year = "2019",
month = may,
language = "English",
volume = "3",
pages = "e1800329",
journal = "ADV BIOSYST",
issn = "2366-7478",
publisher = "Wiley-VCH Verlag GmbH",
number = "5",

}

RIS

TY - JOUR

T1 - Microscaffolds by Direct Laser Writing for Neurite Guidance Leading to Tailor-Made Neuronal Networks

AU - Fendler, Cornelius

AU - Denker, Christian

AU - Harberts , Jann

AU - Bayat, Parisa

AU - Zierold, Robert

AU - Loers, Gabriele

AU - Münzenberg , Markus

AU - Blick, Robert H

PY - 2019/5

Y1 - 2019/5

N2 - While modern day integrated electronic circuits are essentially designed in a 2D fashion, the brain can be regarded as a 3D circuit. The thus enhanced connectivity enables much more complex signal processing as compared to conventional 2D circuits. Recent technological advances in the development of nano/microscale 3D structuring have led to the development of artificial neuron culturing platforms, which surpass the possibilities of classical 2D cultures. In this work, in vitro culturing of neuronal networks is demonstrated by determining predefined pathways through topological and chemical neurite guiding. Tailor-made culturing substrates of microtowers and freestanding microtubes are fabricated using direct laser writing by two-photon polymerization. The first scaffold design that allows for site-specific cell attachment and directed outgrowth of single neurites along defined paths that can be arranged freely in all dimensions, to build neuronal networks with low cell density, is presented. The neurons cultured in the scaffolds show characteristic electrophysiological properties of vital cells after 10 d in vitro. The introduced scaffold design offers a promising concept for future complex neuronal network studies on defined neuronal circuits with tailor-made design specific neurite connections beyond 2D.

AB - While modern day integrated electronic circuits are essentially designed in a 2D fashion, the brain can be regarded as a 3D circuit. The thus enhanced connectivity enables much more complex signal processing as compared to conventional 2D circuits. Recent technological advances in the development of nano/microscale 3D structuring have led to the development of artificial neuron culturing platforms, which surpass the possibilities of classical 2D cultures. In this work, in vitro culturing of neuronal networks is demonstrated by determining predefined pathways through topological and chemical neurite guiding. Tailor-made culturing substrates of microtowers and freestanding microtubes are fabricated using direct laser writing by two-photon polymerization. The first scaffold design that allows for site-specific cell attachment and directed outgrowth of single neurites along defined paths that can be arranged freely in all dimensions, to build neuronal networks with low cell density, is presented. The neurons cultured in the scaffolds show characteristic electrophysiological properties of vital cells after 10 d in vitro. The introduced scaffold design offers a promising concept for future complex neuronal network studies on defined neuronal circuits with tailor-made design specific neurite connections beyond 2D.

M3 - SCORING: Journal article

VL - 3

SP - e1800329

JO - ADV BIOSYST

JF - ADV BIOSYST

SN - 2366-7478

IS - 5

ER -