This title appears in the Scientific Report :
2019
Please use the identifier:
http://dx.doi.org/10.3390/mi10100659 in citations.
Please use the identifier: http://hdl.handle.net/2128/23944 in citations.
Improvements of microcontact printing for micropatterned cell growth by contrast enhancements
Improvements of microcontact printing for micropatterned cell growth by contrast enhancements
Patterned neuronal cell cultures are important tools for investigating neuronal signal integration, network function, and cell–substrate interactions. Because of the variable nature of neuronal cells, the widely used coating method of microcontact printing is in constant need of improvements and ada...
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Personal Name(s): | Hondrich, Timm J. J. |
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Deußen, Oliver / Grannemann, Caroline / Brinkmann, Dominik / Offenhäusser, Andreas (Corresponding author) | |
Contributing Institute: |
Bioelektronik; ICS-8 |
Published in: | Micromachines, 10 (2019) 10, S. 659 - |
Imprint: |
Basel
MDPI
2019
|
DOI: |
10.3390/mi10100659 |
PubMed ID: |
31574944 |
Document Type: |
Journal Article |
Research Program: |
Engineering Cell Function |
Link: |
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Publikationsportal JuSER |
Please use the identifier: http://hdl.handle.net/2128/23944 in citations.
Patterned neuronal cell cultures are important tools for investigating neuronal signal integration, network function, and cell–substrate interactions. Because of the variable nature of neuronal cells, the widely used coating method of microcontact printing is in constant need of improvements and adaptations depending on the pattern, cell type, and coating solutions available for a certain experimental system. In this work, we report on three approaches to modify microcontact printing on borosilicate glass surfaces, which we evaluate with contact angle measurements and by determining the quality of patterned neuronal growth. Although background toxification with manganese salt does not result in the desired pattern enhancement, a simple heat treatment of the glass substrates leads to improved background hydrophobicity and therefore neuronal patterning. Thirdly, we extended a microcontact printing process based on covalently linking the glass surface and the coating molecule via an epoxysilane. This extension is an additional hydrophobization step with dodecylamine. We demonstrate that shelf life of the silanized glass is at least 22 weeks, leading to consistently reliable neuronal patterning by microcontact printing. Thus, we compared three practical additions to microcontact printing, two of which can easily be implemented into a workflow for the investigation of patterned neuronal networks |