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27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells
Purified microtubules have been shown to align along the static magnetic field (SMF) in vitro because of their diamagnetic anisotropy. However, whether mitotic spindle in mammalian cells can be aligned by magnetic field has not been experimentally proved. In particular, the biological effects of SMF...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370190/ https://www.ncbi.nlm.nih.gov/pubmed/28244368 http://dx.doi.org/10.7554/eLife.22911 |
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author | Zhang, Lei Hou, Yubin Li, Zhiyuan Ji, Xinmiao Wang, Ze Wang, Huizhen Tian, Xiaofei Yu, Fazhi Yang, Zhenye Pi, Li Mitchison, Timothy J Lu, Qingyou Zhang, Xin |
author_facet | Zhang, Lei Hou, Yubin Li, Zhiyuan Ji, Xinmiao Wang, Ze Wang, Huizhen Tian, Xiaofei Yu, Fazhi Yang, Zhenye Pi, Li Mitchison, Timothy J Lu, Qingyou Zhang, Xin |
author_sort | Zhang, Lei |
collection | PubMed |
description | Purified microtubules have been shown to align along the static magnetic field (SMF) in vitro because of their diamagnetic anisotropy. However, whether mitotic spindle in mammalian cells can be aligned by magnetic field has not been experimentally proved. In particular, the biological effects of SMF of above 20 T (Tesla) on mammalian cells have never been reported. Here we found that in both CNE-2Z and RPE1 human cells spindle orients in 27 T SMF. The direction of spindle alignment depended on the extent to which chromosomes were aligned to form a planar metaphase plate. Our results show that the magnetic torque acts on both microtubules and chromosomes, and the preferred direction of spindle alignment relative to the field depends more on chromosome alignment than microtubules. In addition, spindle morphology was also perturbed by 27 T SMF. This is the first reported study that investigated the mammalian cellular responses to ultra-high magnetic field of above 20 T. Our study not only found that ultra-high magnetic field can change the orientation and morphology of mitotic spindles, but also provided a tool to probe the role of spindle orientation and perturbation in developmental and cancer biology. DOI: http://dx.doi.org/10.7554/eLife.22911.001 |
format | Online Article Text |
id | pubmed-5370190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53701902017-03-29 27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells Zhang, Lei Hou, Yubin Li, Zhiyuan Ji, Xinmiao Wang, Ze Wang, Huizhen Tian, Xiaofei Yu, Fazhi Yang, Zhenye Pi, Li Mitchison, Timothy J Lu, Qingyou Zhang, Xin eLife Biophysics and Structural Biology Purified microtubules have been shown to align along the static magnetic field (SMF) in vitro because of their diamagnetic anisotropy. However, whether mitotic spindle in mammalian cells can be aligned by magnetic field has not been experimentally proved. In particular, the biological effects of SMF of above 20 T (Tesla) on mammalian cells have never been reported. Here we found that in both CNE-2Z and RPE1 human cells spindle orients in 27 T SMF. The direction of spindle alignment depended on the extent to which chromosomes were aligned to form a planar metaphase plate. Our results show that the magnetic torque acts on both microtubules and chromosomes, and the preferred direction of spindle alignment relative to the field depends more on chromosome alignment than microtubules. In addition, spindle morphology was also perturbed by 27 T SMF. This is the first reported study that investigated the mammalian cellular responses to ultra-high magnetic field of above 20 T. Our study not only found that ultra-high magnetic field can change the orientation and morphology of mitotic spindles, but also provided a tool to probe the role of spindle orientation and perturbation in developmental and cancer biology. DOI: http://dx.doi.org/10.7554/eLife.22911.001 eLife Sciences Publications, Ltd 2017-02-28 /pmc/articles/PMC5370190/ /pubmed/28244368 http://dx.doi.org/10.7554/eLife.22911 Text en © 2017, Zhang et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Zhang, Lei Hou, Yubin Li, Zhiyuan Ji, Xinmiao Wang, Ze Wang, Huizhen Tian, Xiaofei Yu, Fazhi Yang, Zhenye Pi, Li Mitchison, Timothy J Lu, Qingyou Zhang, Xin 27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells |
title | 27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells |
title_full | 27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells |
title_fullStr | 27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells |
title_full_unstemmed | 27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells |
title_short | 27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells |
title_sort | 27 t ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370190/ https://www.ncbi.nlm.nih.gov/pubmed/28244368 http://dx.doi.org/10.7554/eLife.22911 |
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