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PeakForce Tapping resolves individual microvilli on living cells
Microvilli are a common structure found on epithelial cells that increase the apical surface thus enhancing the transmembrane transport capacity and also serve as one of the cell's mechanosensors. These structures are composed of microfilaments and cytoplasm, covered by plasma membrane. Epithel...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054848/ https://www.ncbi.nlm.nih.gov/pubmed/26414320 http://dx.doi.org/10.1002/jmr.2510 |
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author | Schillers, Hermann Medalsy, Izhar Hu, Shuiqing Slade, Andrea L. Shaw, James E. |
author_facet | Schillers, Hermann Medalsy, Izhar Hu, Shuiqing Slade, Andrea L. Shaw, James E. |
author_sort | Schillers, Hermann |
collection | PubMed |
description | Microvilli are a common structure found on epithelial cells that increase the apical surface thus enhancing the transmembrane transport capacity and also serve as one of the cell's mechanosensors. These structures are composed of microfilaments and cytoplasm, covered by plasma membrane. Epithelial cell function is usually coupled to the density of microvilli and its individual size illustrated by diseases, in which microvilli degradation causes malabsorption and diarrhea. Atomic force microscopy (AFM) has been widely used to study the topography and morphology of living cells. Visualizing soft and flexible structures such as microvilli on the apical surface of a live cell has been very challenging because the native microvilli structures are displaced and deformed by the interaction with the probe. PeakForce Tapping® is an AFM imaging mode, which allows reducing tip–sample interactions in time (microseconds) and controlling force in the low pico‐Newton range. Data acquisition of this mode was optimized by using a newly developed PeakForce QNM‐Live Cell probe, having a short cantilever with a 17‐µm‐long tip that minimizes hydrodynamic effects between the cantilever and the sample surface. In this paper, we have demonstrated for the first time the visualization of the microvilli on living kidney cells with AFM using PeakForce Tapping. The structures observed display a force dependence representing either the whole microvilli or just the tips of the microvilli layer. Together, PeakForce Tapping allows force control in the low pico‐Newton range and enables the visualization of very soft and flexible structures on living cells under physiological conditions. © 2015 The Authors Journal of Molecular Recognition Published by John Wiley & Sons Ltd. |
format | Online Article Text |
id | pubmed-5054848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50548482016-10-19 PeakForce Tapping resolves individual microvilli on living cells Schillers, Hermann Medalsy, Izhar Hu, Shuiqing Slade, Andrea L. Shaw, James E. J Mol Recognit Special Issue Article Microvilli are a common structure found on epithelial cells that increase the apical surface thus enhancing the transmembrane transport capacity and also serve as one of the cell's mechanosensors. These structures are composed of microfilaments and cytoplasm, covered by plasma membrane. Epithelial cell function is usually coupled to the density of microvilli and its individual size illustrated by diseases, in which microvilli degradation causes malabsorption and diarrhea. Atomic force microscopy (AFM) has been widely used to study the topography and morphology of living cells. Visualizing soft and flexible structures such as microvilli on the apical surface of a live cell has been very challenging because the native microvilli structures are displaced and deformed by the interaction with the probe. PeakForce Tapping® is an AFM imaging mode, which allows reducing tip–sample interactions in time (microseconds) and controlling force in the low pico‐Newton range. Data acquisition of this mode was optimized by using a newly developed PeakForce QNM‐Live Cell probe, having a short cantilever with a 17‐µm‐long tip that minimizes hydrodynamic effects between the cantilever and the sample surface. In this paper, we have demonstrated for the first time the visualization of the microvilli on living kidney cells with AFM using PeakForce Tapping. The structures observed display a force dependence representing either the whole microvilli or just the tips of the microvilli layer. Together, PeakForce Tapping allows force control in the low pico‐Newton range and enables the visualization of very soft and flexible structures on living cells under physiological conditions. © 2015 The Authors Journal of Molecular Recognition Published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2015-09-28 2016-02 /pmc/articles/PMC5054848/ /pubmed/26414320 http://dx.doi.org/10.1002/jmr.2510 Text en © 2015 The Authors Journal of Molecular Recognition Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Special Issue Article Schillers, Hermann Medalsy, Izhar Hu, Shuiqing Slade, Andrea L. Shaw, James E. PeakForce Tapping resolves individual microvilli on living cells |
title | PeakForce Tapping resolves individual microvilli on living cells
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title_full | PeakForce Tapping resolves individual microvilli on living cells
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title_fullStr | PeakForce Tapping resolves individual microvilli on living cells
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title_full_unstemmed | PeakForce Tapping resolves individual microvilli on living cells
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title_short | PeakForce Tapping resolves individual microvilli on living cells
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title_sort | peakforce tapping resolves individual microvilli on living cells |
topic | Special Issue Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054848/ https://www.ncbi.nlm.nih.gov/pubmed/26414320 http://dx.doi.org/10.1002/jmr.2510 |
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