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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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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