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Cell Patterning on Photolithographically Defined Parylene-C: SiO(2) Substrates
Cell patterning platforms support broad research goals, such as construction of predefined in vitro neuronal networks and the exploration of certain central aspects of cellular physiology. To easily combine cell patterning with Multi-Electrode Arrays (MEAs) and silicon-based ‘lab on a chip’ technolo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143168/ https://www.ncbi.nlm.nih.gov/pubmed/24637580 http://dx.doi.org/10.3791/50929 |
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author | Hughes, Mark A. Brennan, Paul M. Bunting, Andrew S. Shipston, Mike J. Murray, Alan F. |
author_facet | Hughes, Mark A. Brennan, Paul M. Bunting, Andrew S. Shipston, Mike J. Murray, Alan F. |
author_sort | Hughes, Mark A. |
collection | PubMed |
description | Cell patterning platforms support broad research goals, such as construction of predefined in vitro neuronal networks and the exploration of certain central aspects of cellular physiology. To easily combine cell patterning with Multi-Electrode Arrays (MEAs) and silicon-based ‘lab on a chip’ technologies, a microfabrication-compatible protocol is required. We describe a method that utilizes deposition of the polymer parylene-C on SiO(2 )wafers. Photolithography enables accurate and reliable patterning of parylene-C at micron-level resolution. Subsequent activation by immersion in fetal bovine serum (or another specific activation solution) results in a substrate in which cultured cells adhere to, or are repulsed by, parylene or SiO(2) regions respectively. This technique has allowed patterning of a broad range of cell types (including primary murine hippocampal cells, HEK 293 cell line, human neuron-like teratocarcinoma cell line, primary murine cerebellar granule cells, and primary human glioma-derived stem-like cells). Interestingly, however, the platform is not universal; reflecting the importance of cell-specific adhesion molecules. This cell patterning process is cost effective, reliable, and importantly can be incorporated into standard microfabrication (chip manufacturing) protocols, paving the way for integration of microelectronic technology. |
format | Online Article Text |
id | pubmed-4143168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41431682014-08-27 Cell Patterning on Photolithographically Defined Parylene-C: SiO(2) Substrates Hughes, Mark A. Brennan, Paul M. Bunting, Andrew S. Shipston, Mike J. Murray, Alan F. J Vis Exp Bioengineering Cell patterning platforms support broad research goals, such as construction of predefined in vitro neuronal networks and the exploration of certain central aspects of cellular physiology. To easily combine cell patterning with Multi-Electrode Arrays (MEAs) and silicon-based ‘lab on a chip’ technologies, a microfabrication-compatible protocol is required. We describe a method that utilizes deposition of the polymer parylene-C on SiO(2 )wafers. Photolithography enables accurate and reliable patterning of parylene-C at micron-level resolution. Subsequent activation by immersion in fetal bovine serum (or another specific activation solution) results in a substrate in which cultured cells adhere to, or are repulsed by, parylene or SiO(2) regions respectively. This technique has allowed patterning of a broad range of cell types (including primary murine hippocampal cells, HEK 293 cell line, human neuron-like teratocarcinoma cell line, primary murine cerebellar granule cells, and primary human glioma-derived stem-like cells). Interestingly, however, the platform is not universal; reflecting the importance of cell-specific adhesion molecules. This cell patterning process is cost effective, reliable, and importantly can be incorporated into standard microfabrication (chip manufacturing) protocols, paving the way for integration of microelectronic technology. MyJove Corporation 2014-03-07 /pmc/articles/PMC4143168/ /pubmed/24637580 http://dx.doi.org/10.3791/50929 Text en Copyright © 2014, Journal of Visualized Experiments http://creativecommons.org/licenses/by/3.0/us/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 License. To view a copy of this license, visithttp://creativecommons.org/licenses/by/3.0/us/ |
spellingShingle | Bioengineering Hughes, Mark A. Brennan, Paul M. Bunting, Andrew S. Shipston, Mike J. Murray, Alan F. Cell Patterning on Photolithographically Defined Parylene-C: SiO(2) Substrates |
title | Cell Patterning on Photolithographically Defined Parylene-C: SiO(2) Substrates |
title_full | Cell Patterning on Photolithographically Defined Parylene-C: SiO(2) Substrates |
title_fullStr | Cell Patterning on Photolithographically Defined Parylene-C: SiO(2) Substrates |
title_full_unstemmed | Cell Patterning on Photolithographically Defined Parylene-C: SiO(2) Substrates |
title_short | Cell Patterning on Photolithographically Defined Parylene-C: SiO(2) Substrates |
title_sort | cell patterning on photolithographically defined parylene-c: sio(2) substrates |
topic | Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143168/ https://www.ncbi.nlm.nih.gov/pubmed/24637580 http://dx.doi.org/10.3791/50929 |
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