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The flexibility and dynamics of the tubules in the endoplasmic reticulum
The endoplasmic reticulum (ER) is a single organelle in eukaryotic cells that extends throughout the cell and is involved in a large number of cellular functions. Using a combination of fixed and live cells (human MRC5 lung cells) in diffraction limited and super-resolved fluorescence microscopy (ST...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705721/ https://www.ncbi.nlm.nih.gov/pubmed/29184084 http://dx.doi.org/10.1038/s41598-017-16570-4 |
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author | Georgiades, Pantelis Allan, Victoria J. Wright, Graham D. Woodman, Philip G. Udommai, Parinya Chung, Manloeng A. Waigh, Thomas A. |
author_facet | Georgiades, Pantelis Allan, Victoria J. Wright, Graham D. Woodman, Philip G. Udommai, Parinya Chung, Manloeng A. Waigh, Thomas A. |
author_sort | Georgiades, Pantelis |
collection | PubMed |
description | The endoplasmic reticulum (ER) is a single organelle in eukaryotic cells that extends throughout the cell and is involved in a large number of cellular functions. Using a combination of fixed and live cells (human MRC5 lung cells) in diffraction limited and super-resolved fluorescence microscopy (STORM) experiments, we determined that the average persistence length of the ER tubules was 3.03 ± 0.24 μm. Removing the branched network junctions from the analysis caused a slight increase in the average persistence length to 4.71 ± 0.14 μm, and provides the tubule’s persistence length with a moderate length scale dependence. The average radius of the tubules was 44.1 ± 3.2 nm. The bending rigidity of the ER tubule membranes was found to be 10.9 ± 1.2 kT (17.0 ± 1.3 kT without branch points). We investigated the dynamic behaviour of ER tubules in live cells, and found that the ER tubules behaved like semi-flexible fibres under tension. The majority of the ER tubules experienced equilibrium transverse fluctuations under tension, whereas a minority number of them had active super-diffusive motions driven by motor proteins. Cells thus actively modulate the dynamics of the ER in a well-defined manner, which is expected in turn to impact on its many functions. |
format | Online Article Text |
id | pubmed-5705721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57057212017-12-05 The flexibility and dynamics of the tubules in the endoplasmic reticulum Georgiades, Pantelis Allan, Victoria J. Wright, Graham D. Woodman, Philip G. Udommai, Parinya Chung, Manloeng A. Waigh, Thomas A. Sci Rep Article The endoplasmic reticulum (ER) is a single organelle in eukaryotic cells that extends throughout the cell and is involved in a large number of cellular functions. Using a combination of fixed and live cells (human MRC5 lung cells) in diffraction limited and super-resolved fluorescence microscopy (STORM) experiments, we determined that the average persistence length of the ER tubules was 3.03 ± 0.24 μm. Removing the branched network junctions from the analysis caused a slight increase in the average persistence length to 4.71 ± 0.14 μm, and provides the tubule’s persistence length with a moderate length scale dependence. The average radius of the tubules was 44.1 ± 3.2 nm. The bending rigidity of the ER tubule membranes was found to be 10.9 ± 1.2 kT (17.0 ± 1.3 kT without branch points). We investigated the dynamic behaviour of ER tubules in live cells, and found that the ER tubules behaved like semi-flexible fibres under tension. The majority of the ER tubules experienced equilibrium transverse fluctuations under tension, whereas a minority number of them had active super-diffusive motions driven by motor proteins. Cells thus actively modulate the dynamics of the ER in a well-defined manner, which is expected in turn to impact on its many functions. Nature Publishing Group UK 2017-11-28 /pmc/articles/PMC5705721/ /pubmed/29184084 http://dx.doi.org/10.1038/s41598-017-16570-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Georgiades, Pantelis Allan, Victoria J. Wright, Graham D. Woodman, Philip G. Udommai, Parinya Chung, Manloeng A. Waigh, Thomas A. The flexibility and dynamics of the tubules in the endoplasmic reticulum |
title | The flexibility and dynamics of the tubules in the endoplasmic reticulum |
title_full | The flexibility and dynamics of the tubules in the endoplasmic reticulum |
title_fullStr | The flexibility and dynamics of the tubules in the endoplasmic reticulum |
title_full_unstemmed | The flexibility and dynamics of the tubules in the endoplasmic reticulum |
title_short | The flexibility and dynamics of the tubules in the endoplasmic reticulum |
title_sort | flexibility and dynamics of the tubules in the endoplasmic reticulum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705721/ https://www.ncbi.nlm.nih.gov/pubmed/29184084 http://dx.doi.org/10.1038/s41598-017-16570-4 |
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