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Size-Tunable Nanoneedle Arrays for Influencing Stem Cell Morphology, Gene Expression, and Nuclear Membrane Curvature
[Image: see text] High-aspect-ratio nanostructures have emerged as versatile platforms for intracellular sensing and biomolecule delivery. Here, we present a microfabrication approach in which a combination of reactive ion etching protocols were used to produce high-aspect-ratio, nondegradable silic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254837/ https://www.ncbi.nlm.nih.gov/pubmed/32330008 http://dx.doi.org/10.1021/acsnano.9b08689 |
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author | Seong, Hyejeong Higgins, Stuart G. Penders, Jelle Armstrong, James P. K. Crowder, Spencer W. Moore, Axel C. Sero, Julia E. Becce, Michele Stevens, Molly M. |
author_facet | Seong, Hyejeong Higgins, Stuart G. Penders, Jelle Armstrong, James P. K. Crowder, Spencer W. Moore, Axel C. Sero, Julia E. Becce, Michele Stevens, Molly M. |
author_sort | Seong, Hyejeong |
collection | PubMed |
description | [Image: see text] High-aspect-ratio nanostructures have emerged as versatile platforms for intracellular sensing and biomolecule delivery. Here, we present a microfabrication approach in which a combination of reactive ion etching protocols were used to produce high-aspect-ratio, nondegradable silicon nanoneedle arrays with tip diameters that could be finely tuned between 20 and 700 nm. We used these arrays to guide the long-term culture of human mesenchymal stem cells (hMSCs). Notably, we used changes in the nanoneedle tip diameter to control the morphology, nuclear size, and F-actin alignment of interfaced hMSCs and to regulate the expression of nuclear lamina genes, Yes-associated protein (YAP) target genes, and focal adhesion genes. These topography-driven changes were attributed to signaling by Rho-family GTPase pathways, differences in the effective stiffness of the nanoneedle arrays, and the degree of nuclear membrane impingement, with the latter clearly visualized using focused ion beam scanning electron microscopy (FIB-SEM). Our approach to design high-aspect-ratio nanostructures will be broadly applicable to design biomaterials and biomedical devices used for long-term cell stimulation and monitoring. |
format | Online Article Text |
id | pubmed-7254837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-72548372020-05-29 Size-Tunable Nanoneedle Arrays for Influencing Stem Cell Morphology, Gene Expression, and Nuclear Membrane Curvature Seong, Hyejeong Higgins, Stuart G. Penders, Jelle Armstrong, James P. K. Crowder, Spencer W. Moore, Axel C. Sero, Julia E. Becce, Michele Stevens, Molly M. ACS Nano [Image: see text] High-aspect-ratio nanostructures have emerged as versatile platforms for intracellular sensing and biomolecule delivery. Here, we present a microfabrication approach in which a combination of reactive ion etching protocols were used to produce high-aspect-ratio, nondegradable silicon nanoneedle arrays with tip diameters that could be finely tuned between 20 and 700 nm. We used these arrays to guide the long-term culture of human mesenchymal stem cells (hMSCs). Notably, we used changes in the nanoneedle tip diameter to control the morphology, nuclear size, and F-actin alignment of interfaced hMSCs and to regulate the expression of nuclear lamina genes, Yes-associated protein (YAP) target genes, and focal adhesion genes. These topography-driven changes were attributed to signaling by Rho-family GTPase pathways, differences in the effective stiffness of the nanoneedle arrays, and the degree of nuclear membrane impingement, with the latter clearly visualized using focused ion beam scanning electron microscopy (FIB-SEM). Our approach to design high-aspect-ratio nanostructures will be broadly applicable to design biomaterials and biomedical devices used for long-term cell stimulation and monitoring. American Chemical Society 2020-04-24 2020-05-26 /pmc/articles/PMC7254837/ /pubmed/32330008 http://dx.doi.org/10.1021/acsnano.9b08689 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Seong, Hyejeong Higgins, Stuart G. Penders, Jelle Armstrong, James P. K. Crowder, Spencer W. Moore, Axel C. Sero, Julia E. Becce, Michele Stevens, Molly M. Size-Tunable Nanoneedle Arrays for Influencing Stem Cell Morphology, Gene Expression, and Nuclear Membrane Curvature |
title | Size-Tunable
Nanoneedle Arrays for Influencing Stem
Cell Morphology, Gene Expression, and Nuclear Membrane Curvature |
title_full | Size-Tunable
Nanoneedle Arrays for Influencing Stem
Cell Morphology, Gene Expression, and Nuclear Membrane Curvature |
title_fullStr | Size-Tunable
Nanoneedle Arrays for Influencing Stem
Cell Morphology, Gene Expression, and Nuclear Membrane Curvature |
title_full_unstemmed | Size-Tunable
Nanoneedle Arrays for Influencing Stem
Cell Morphology, Gene Expression, and Nuclear Membrane Curvature |
title_short | Size-Tunable
Nanoneedle Arrays for Influencing Stem
Cell Morphology, Gene Expression, and Nuclear Membrane Curvature |
title_sort | size-tunable
nanoneedle arrays for influencing stem
cell morphology, gene expression, and nuclear membrane curvature |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254837/ https://www.ncbi.nlm.nih.gov/pubmed/32330008 http://dx.doi.org/10.1021/acsnano.9b08689 |
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