27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells

  1. Lei Zhang
  2. Yubin Hou
  3. Zhiyuan Li
  4. Xinmiao Ji
  5. Ze Wang
  6. Huizhen Wang
  7. Xiaofei Tian
  8. Fazhi Yu
  9. Zhenye Yang
  10. Li Pi
  11. Timothy J Mitchison
  12. Qingyou Lu  Is a corresponding author
  13. Xin Zhang  Is a corresponding author
  1. Chinese Academy of Sciences, China
  2. University of Science and Technology of China, China
  3. Harvard Medical School, United States

Abstract

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 cells can be aligned by magnetic field has not been experimentally proved. In particular, the biological effects of SMF of above 20 T (Tesla) 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 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.

Article and author information

Author details

  1. Lei Zhang

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  2. Yubin Hou

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  3. Zhiyuan Li

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  4. Xinmiao Ji

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  5. Ze Wang

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  6. Huizhen Wang

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  7. Xiaofei Tian

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  8. Fazhi Yu

    University of Science and Technology of China, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  9. Zhenye Yang

    University of Science and Technology of China, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  10. Li Pi

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    Competing interests
    The authors declare that no competing interests exist.
  11. Timothy J Mitchison

    Department of Systems Biology, Harvard Medical School, Boston, United States
    Competing interests
    The authors declare that no competing interests exist.
  12. Qingyou Lu

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    For correspondence
    qxl@ustc.edu.cn
    Competing interests
    The authors declare that no competing interests exist.
  13. Xin Zhang

    High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, China
    For correspondence
    xinzhang@hmfl.ac.cn
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-3499-2189

Funding

national key research and development program of china (#2016YFA0400900)

  • Xin Zhang

National Natural Science Foundation of China (U1532151)

  • Xin Zhang

Hefei Science Center (2016HSC-IU007)

  • Xin Zhang

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Copyright

© 2017, Zhang et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 3,488
    views
  • 622
    downloads
  • 66
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Lei Zhang
  2. Yubin Hou
  3. Zhiyuan Li
  4. Xinmiao Ji
  5. Ze Wang
  6. Huizhen Wang
  7. Xiaofei Tian
  8. Fazhi Yu
  9. Zhenye Yang
  10. Li Pi
  11. Timothy J Mitchison
  12. Qingyou Lu
  13. Xin Zhang
(2017)
27 T ultra-high static magnetic field changes orientation and morphology of mitotic spindles in human cells
eLife 6:e22911.
https://doi.org/10.7554/eLife.22911

Share this article

https://doi.org/10.7554/eLife.22911

Further reading

    1. Developmental Biology
    2. Physics of Living Systems
    Fridtjof Brauns, Nikolas H Claussen ... Boris I Shraiman
    Research Article

    Shape changes of epithelia during animal development, such as convergent extension, are achieved through the concerted mechanical activity of individual cells. While much is known about the corresponding large-scale tissue flow and its genetic drivers, fundamental questions regarding local control of contractile activity on the cellular scale and its embryo-scale coordination remain open. To address these questions, we develop a quantitative, model-based analysis framework to relate cell geometry to local tension in recently obtained time-lapse imaging data of gastrulating Drosophila embryos. This analysis systematically decomposes cell shape changes and T1 rearrangements into internally driven, active, and externally driven, passive, contributions. Our analysis provides evidence that germ band extension is driven by active T1 processes that self-organize through positive feedback acting on tensions. More generally, our findings suggest that epithelial convergent extension results from the controlled transformation of internal force balance geometry which combines the effects of bottom-up local self-organization with the top-down, embryo-scale regulation by gene expression.