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Nanoneedle-Mediated Stimulation of Cell Mechanotransduction Machinery
[Image: see text] Biomaterial substrates can be engineered to present topographical signals to cells which, through interactions between the material and active components of the cell membrane, regulate key cellular processes and guide cell fate decisions. However, targeting mechanoresponsive elemen...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439438/ https://www.ncbi.nlm.nih.gov/pubmed/30829469 http://dx.doi.org/10.1021/acsnano.8b06998 |
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author | Hansel, Catherine S. Crowder, Spencer W. Cooper, Samuel Gopal, Sahana João Pardelha da Cruz, Maria de Oliveira Martins, Leonardo Keller, Debora Rothery, Stephen Becce, Michele Cass, Anthony E. G. Bakal, Chris Chiappini, Ciro Stevens, Molly M. |
author_facet | Hansel, Catherine S. Crowder, Spencer W. Cooper, Samuel Gopal, Sahana João Pardelha da Cruz, Maria de Oliveira Martins, Leonardo Keller, Debora Rothery, Stephen Becce, Michele Cass, Anthony E. G. Bakal, Chris Chiappini, Ciro Stevens, Molly M. |
author_sort | Hansel, Catherine S. |
collection | PubMed |
description | [Image: see text] Biomaterial substrates can be engineered to present topographical signals to cells which, through interactions between the material and active components of the cell membrane, regulate key cellular processes and guide cell fate decisions. However, targeting mechanoresponsive elements that reside within the intracellular domain is a concept that has only recently emerged. Here, we show that mesoporous silicon nanoneedle arrays interact simultaneously with the cell membrane, cytoskeleton, and nucleus of primary human cells, generating distinct responses at each of these cellular compartments. Specifically, nanoneedles inhibit focal adhesion maturation at the membrane, reduce tension in the cytoskeleton, and lead to remodeling of the nuclear envelope at sites of impingement. The combined changes in actin cytoskeleton assembly, expression and segregation of the nuclear lamina, and localization of Yes-associated protein (YAP) correlate differently from what is canonically observed upon stimulation at the cell membrane, revealing that biophysical cues directed to the intracellular space can generate heretofore unobserved mechanosensory responses. These findings highlight the ability of nanoneedles to study and direct the phenotype of large cell populations simultaneously, through biophysical interactions with multiple mechanoresponsive components. |
format | Online Article Text |
id | pubmed-6439438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-64394382019-04-01 Nanoneedle-Mediated Stimulation of Cell Mechanotransduction Machinery Hansel, Catherine S. Crowder, Spencer W. Cooper, Samuel Gopal, Sahana João Pardelha da Cruz, Maria de Oliveira Martins, Leonardo Keller, Debora Rothery, Stephen Becce, Michele Cass, Anthony E. G. Bakal, Chris Chiappini, Ciro Stevens, Molly M. ACS Nano [Image: see text] Biomaterial substrates can be engineered to present topographical signals to cells which, through interactions between the material and active components of the cell membrane, regulate key cellular processes and guide cell fate decisions. However, targeting mechanoresponsive elements that reside within the intracellular domain is a concept that has only recently emerged. Here, we show that mesoporous silicon nanoneedle arrays interact simultaneously with the cell membrane, cytoskeleton, and nucleus of primary human cells, generating distinct responses at each of these cellular compartments. Specifically, nanoneedles inhibit focal adhesion maturation at the membrane, reduce tension in the cytoskeleton, and lead to remodeling of the nuclear envelope at sites of impingement. The combined changes in actin cytoskeleton assembly, expression and segregation of the nuclear lamina, and localization of Yes-associated protein (YAP) correlate differently from what is canonically observed upon stimulation at the cell membrane, revealing that biophysical cues directed to the intracellular space can generate heretofore unobserved mechanosensory responses. These findings highlight the ability of nanoneedles to study and direct the phenotype of large cell populations simultaneously, through biophysical interactions with multiple mechanoresponsive components. American Chemical Society 2019-03-04 2019-03-26 /pmc/articles/PMC6439438/ /pubmed/30829469 http://dx.doi.org/10.1021/acsnano.8b06998 Text en Copyright © 2019 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 | Hansel, Catherine S. Crowder, Spencer W. Cooper, Samuel Gopal, Sahana João Pardelha da Cruz, Maria de Oliveira Martins, Leonardo Keller, Debora Rothery, Stephen Becce, Michele Cass, Anthony E. G. Bakal, Chris Chiappini, Ciro Stevens, Molly M. Nanoneedle-Mediated Stimulation of Cell Mechanotransduction Machinery |
title | Nanoneedle-Mediated Stimulation of Cell Mechanotransduction
Machinery |
title_full | Nanoneedle-Mediated Stimulation of Cell Mechanotransduction
Machinery |
title_fullStr | Nanoneedle-Mediated Stimulation of Cell Mechanotransduction
Machinery |
title_full_unstemmed | Nanoneedle-Mediated Stimulation of Cell Mechanotransduction
Machinery |
title_short | Nanoneedle-Mediated Stimulation of Cell Mechanotransduction
Machinery |
title_sort | nanoneedle-mediated stimulation of cell mechanotransduction
machinery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439438/ https://www.ncbi.nlm.nih.gov/pubmed/30829469 http://dx.doi.org/10.1021/acsnano.8b06998 |
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