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Biological reaction control using topography regulation of nanostructured titanium
The micro- and nanosize surface topography of dental implants has been shown to affect the growth of surrounding cells. In this study, standardized and controlled periodic nanopatterns were fabricated with nanosized surface roughness on titanium substrates, and their influence on bone marrow stromal...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016147/ https://www.ncbi.nlm.nih.gov/pubmed/32051472 http://dx.doi.org/10.1038/s41598-020-59395-4 |
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author | Shiozawa, Mayuko Takeuchi, Haruka Akiba, Yosuke Eguchi, Kaori Akiba, Nami Aoyagi, Yujin Nagasawa, Masako Kuwae, Hiroyuki Izumi, Kenji Uoshima, Katsumi Mizuno, Jun |
author_facet | Shiozawa, Mayuko Takeuchi, Haruka Akiba, Yosuke Eguchi, Kaori Akiba, Nami Aoyagi, Yujin Nagasawa, Masako Kuwae, Hiroyuki Izumi, Kenji Uoshima, Katsumi Mizuno, Jun |
author_sort | Shiozawa, Mayuko |
collection | PubMed |
description | The micro- and nanosize surface topography of dental implants has been shown to affect the growth of surrounding cells. In this study, standardized and controlled periodic nanopatterns were fabricated with nanosized surface roughness on titanium substrates, and their influence on bone marrow stromal cells investigated. Cell proliferation assays revealed that the bare substrate with a 1.7 nm surface roughness has lower hydrophilicity but higher proliferation ability than that with a 0.6 nm surface roughness. Further, with the latter substrate, directional cell growth was observed for line and groove patterns with a width of 100 nm and a height of 50 or 100 nm, but not for those with a height of 10 or 25 nm. With the smooth substrate, time-lapse microscopic analyses showed that more than 80% of the bone marrow cells on the line and groove pattern with a height of 100 nm grew and divided along the lines. As the nanosized grain structure controls the cell proliferation rate and the nanosized line and groove structure (50–100 nm) controls cell migration, division, and growth orientation, these standardized nanosized titanium structures can be used to elucidate the mechanisms by which surface topography regulates tissue responses to biomaterials. |
format | Online Article Text |
id | pubmed-7016147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70161472020-02-21 Biological reaction control using topography regulation of nanostructured titanium Shiozawa, Mayuko Takeuchi, Haruka Akiba, Yosuke Eguchi, Kaori Akiba, Nami Aoyagi, Yujin Nagasawa, Masako Kuwae, Hiroyuki Izumi, Kenji Uoshima, Katsumi Mizuno, Jun Sci Rep Article The micro- and nanosize surface topography of dental implants has been shown to affect the growth of surrounding cells. In this study, standardized and controlled periodic nanopatterns were fabricated with nanosized surface roughness on titanium substrates, and their influence on bone marrow stromal cells investigated. Cell proliferation assays revealed that the bare substrate with a 1.7 nm surface roughness has lower hydrophilicity but higher proliferation ability than that with a 0.6 nm surface roughness. Further, with the latter substrate, directional cell growth was observed for line and groove patterns with a width of 100 nm and a height of 50 or 100 nm, but not for those with a height of 10 or 25 nm. With the smooth substrate, time-lapse microscopic analyses showed that more than 80% of the bone marrow cells on the line and groove pattern with a height of 100 nm grew and divided along the lines. As the nanosized grain structure controls the cell proliferation rate and the nanosized line and groove structure (50–100 nm) controls cell migration, division, and growth orientation, these standardized nanosized titanium structures can be used to elucidate the mechanisms by which surface topography regulates tissue responses to biomaterials. Nature Publishing Group UK 2020-02-12 /pmc/articles/PMC7016147/ /pubmed/32051472 http://dx.doi.org/10.1038/s41598-020-59395-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shiozawa, Mayuko Takeuchi, Haruka Akiba, Yosuke Eguchi, Kaori Akiba, Nami Aoyagi, Yujin Nagasawa, Masako Kuwae, Hiroyuki Izumi, Kenji Uoshima, Katsumi Mizuno, Jun Biological reaction control using topography regulation of nanostructured titanium |
title | Biological reaction control using topography regulation of nanostructured titanium |
title_full | Biological reaction control using topography regulation of nanostructured titanium |
title_fullStr | Biological reaction control using topography regulation of nanostructured titanium |
title_full_unstemmed | Biological reaction control using topography regulation of nanostructured titanium |
title_short | Biological reaction control using topography regulation of nanostructured titanium |
title_sort | biological reaction control using topography regulation of nanostructured titanium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016147/ https://www.ncbi.nlm.nih.gov/pubmed/32051472 http://dx.doi.org/10.1038/s41598-020-59395-4 |
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