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Manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips
Tungsten chemical-mechanical polished integrated circuits were used to study the alignment and immobilization of mammalian (Vero) cells. These devices consist of blanket silicon oxide thin films embedded with micro- and nano-meter scale tungsten metal line structures on the surface. The final surfac...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678500/ https://www.ncbi.nlm.nih.gov/pubmed/29152017 http://dx.doi.org/10.1080/14686996.2017.1388135 |
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author | Moussa, Hassan I. Logan, Megan Siow, Geoffrey C. Phann, Darron L. Rao, Zheng Aucoin, Marc G. Tsui, Ting Y. |
author_facet | Moussa, Hassan I. Logan, Megan Siow, Geoffrey C. Phann, Darron L. Rao, Zheng Aucoin, Marc G. Tsui, Ting Y. |
author_sort | Moussa, Hassan I. |
collection | PubMed |
description | Tungsten chemical-mechanical polished integrated circuits were used to study the alignment and immobilization of mammalian (Vero) cells. These devices consist of blanket silicon oxide thin films embedded with micro- and nano-meter scale tungsten metal line structures on the surface. The final surfaces are extremely flat and smooth across the entire substrate, with a roughness in the order of nanometers. Vero cells were deposited on the surface and allowed to adhere. Microscopy examinations revealed that cells have a strong preference to adhere to tungsten over silicon oxide surfaces with up to 99% of cells adhering to the tungsten portion of the surface. Cells self-aligned and elongated into long threads to maximize contact with isolated tungsten lines as thin as 180 nm. The orientation of the Vero cells showed sensitivity to the tungsten line geometric parameters, such as line width and spacing. Up to 93% of cells on 10 μm wide comb structures were aligned within ± 20° of the metal line axis. In contrast, only ~22% of cells incubated on 0.18 μm comb patterned tungsten lines were oriented within the same angular interval. This phenomenon is explained using a simple model describing cellular geometry as a function of pattern width and spacing, which showed that cells will rearrange their morphology to maximize their contact to the embedded tungsten. Finally, it was discovered that the materials could be reused after cleaning the surfaces, while maintaining cell alignment capability. |
format | Online Article Text |
id | pubmed-5678500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-56785002017-11-17 Manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips Moussa, Hassan I. Logan, Megan Siow, Geoffrey C. Phann, Darron L. Rao, Zheng Aucoin, Marc G. Tsui, Ting Y. Sci Technol Adv Mater Bio-Inspired and Biomedical Materials Tungsten chemical-mechanical polished integrated circuits were used to study the alignment and immobilization of mammalian (Vero) cells. These devices consist of blanket silicon oxide thin films embedded with micro- and nano-meter scale tungsten metal line structures on the surface. The final surfaces are extremely flat and smooth across the entire substrate, with a roughness in the order of nanometers. Vero cells were deposited on the surface and allowed to adhere. Microscopy examinations revealed that cells have a strong preference to adhere to tungsten over silicon oxide surfaces with up to 99% of cells adhering to the tungsten portion of the surface. Cells self-aligned and elongated into long threads to maximize contact with isolated tungsten lines as thin as 180 nm. The orientation of the Vero cells showed sensitivity to the tungsten line geometric parameters, such as line width and spacing. Up to 93% of cells on 10 μm wide comb structures were aligned within ± 20° of the metal line axis. In contrast, only ~22% of cells incubated on 0.18 μm comb patterned tungsten lines were oriented within the same angular interval. This phenomenon is explained using a simple model describing cellular geometry as a function of pattern width and spacing, which showed that cells will rearrange their morphology to maximize their contact to the embedded tungsten. Finally, it was discovered that the materials could be reused after cleaning the surfaces, while maintaining cell alignment capability. Taylor & Francis 2017-10-27 /pmc/articles/PMC5678500/ /pubmed/29152017 http://dx.doi.org/10.1080/14686996.2017.1388135 Text en © 2017 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Bio-Inspired and Biomedical Materials Moussa, Hassan I. Logan, Megan Siow, Geoffrey C. Phann, Darron L. Rao, Zheng Aucoin, Marc G. Tsui, Ting Y. Manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips |
title | Manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips |
title_full | Manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips |
title_fullStr | Manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips |
title_full_unstemmed | Manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips |
title_short | Manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips |
title_sort | manipulating mammalian cell morphologies using chemical-mechanical polished integrated circuit chips |
topic | Bio-Inspired and Biomedical Materials |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678500/ https://www.ncbi.nlm.nih.gov/pubmed/29152017 http://dx.doi.org/10.1080/14686996.2017.1388135 |
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