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Cell Membrane Disruption by Vertical Micro-/Nanopillars: Role of Membrane Bending and Traction Forces
[Image: see text] Gaining access to the cell interior is fundamental for many applications, such as electrical recording and drug and biomolecular delivery. A very promising technique consists of culturing cells on micro-/nanopillars. The tight adhesion and high local deformation of cells in contact...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117743/ https://www.ncbi.nlm.nih.gov/pubmed/30081625 http://dx.doi.org/10.1021/acsami.8b08218 |
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author | Capozza, Rosario Caprettini, Valeria Gonano, Carlo A. Bosca, Alessandro Moia, Fabio Santoro, Francesca De Angelis, Francesco |
author_facet | Capozza, Rosario Caprettini, Valeria Gonano, Carlo A. Bosca, Alessandro Moia, Fabio Santoro, Francesca De Angelis, Francesco |
author_sort | Capozza, Rosario |
collection | PubMed |
description | [Image: see text] Gaining access to the cell interior is fundamental for many applications, such as electrical recording and drug and biomolecular delivery. A very promising technique consists of culturing cells on micro-/nanopillars. The tight adhesion and high local deformation of cells in contact with nanostructures can promote the permeabilization of lipids at the plasma membrane, providing access to the internal compartment. However, there is still much experimental controversy regarding when and how the intracellular environment is targeted and the role of the geometry and interactions with surfaces. Consequently, we investigated, by coarse-grained molecular dynamics simulations of the cell membrane, the mechanical properties of the lipid bilayer under high strain and bending conditions. We found out that a high curvature of the lipid bilayer dramatically lowers the traction force necessary to achieve membrane rupture. Afterward, we experimentally studied the permeabilization rate of the cell membrane by pillars with comparable aspect ratios but different sharpness values at the edges. The experimental data support the simulation results: even pillars with diameters in the micron range may cause local membrane disruption when their edges are sufficiently sharp. Therefore, the permeabilization likelihood is connected to the local geometric features of the pillars rather than diameter or aspect ratio. The present study can also provide significant contributions to the design of three-dimensional biointerfaces for tissue engineering and cellular growth. |
format | Online Article Text |
id | pubmed-6117743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-61177432018-09-04 Cell Membrane Disruption by Vertical Micro-/Nanopillars: Role of Membrane Bending and Traction Forces Capozza, Rosario Caprettini, Valeria Gonano, Carlo A. Bosca, Alessandro Moia, Fabio Santoro, Francesca De Angelis, Francesco ACS Appl Mater Interfaces [Image: see text] Gaining access to the cell interior is fundamental for many applications, such as electrical recording and drug and biomolecular delivery. A very promising technique consists of culturing cells on micro-/nanopillars. The tight adhesion and high local deformation of cells in contact with nanostructures can promote the permeabilization of lipids at the plasma membrane, providing access to the internal compartment. However, there is still much experimental controversy regarding when and how the intracellular environment is targeted and the role of the geometry and interactions with surfaces. Consequently, we investigated, by coarse-grained molecular dynamics simulations of the cell membrane, the mechanical properties of the lipid bilayer under high strain and bending conditions. We found out that a high curvature of the lipid bilayer dramatically lowers the traction force necessary to achieve membrane rupture. Afterward, we experimentally studied the permeabilization rate of the cell membrane by pillars with comparable aspect ratios but different sharpness values at the edges. The experimental data support the simulation results: even pillars with diameters in the micron range may cause local membrane disruption when their edges are sufficiently sharp. Therefore, the permeabilization likelihood is connected to the local geometric features of the pillars rather than diameter or aspect ratio. The present study can also provide significant contributions to the design of three-dimensional biointerfaces for tissue engineering and cellular growth. American Chemical Society 2018-08-07 2018-08-29 /pmc/articles/PMC6117743/ /pubmed/30081625 http://dx.doi.org/10.1021/acsami.8b08218 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Capozza, Rosario Caprettini, Valeria Gonano, Carlo A. Bosca, Alessandro Moia, Fabio Santoro, Francesca De Angelis, Francesco Cell Membrane Disruption by Vertical Micro-/Nanopillars: Role of Membrane Bending and Traction Forces |
title | Cell
Membrane Disruption by Vertical Micro-/Nanopillars:
Role of Membrane Bending and Traction Forces |
title_full | Cell
Membrane Disruption by Vertical Micro-/Nanopillars:
Role of Membrane Bending and Traction Forces |
title_fullStr | Cell
Membrane Disruption by Vertical Micro-/Nanopillars:
Role of Membrane Bending and Traction Forces |
title_full_unstemmed | Cell
Membrane Disruption by Vertical Micro-/Nanopillars:
Role of Membrane Bending and Traction Forces |
title_short | Cell
Membrane Disruption by Vertical Micro-/Nanopillars:
Role of Membrane Bending and Traction Forces |
title_sort | cell
membrane disruption by vertical micro-/nanopillars:
role of membrane bending and traction forces |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117743/ https://www.ncbi.nlm.nih.gov/pubmed/30081625 http://dx.doi.org/10.1021/acsami.8b08218 |
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