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Microtubule organization is determined by the shape of epithelial cells

Author

Listed:
  • Juan Manuel Gomez

    (Development and Neuroscience, and the Gurdon Institute, The University of Cambridge
    Present address: Institute of Genetics, University of Cologne, Cologne 50674, Germany)

  • Lyubov Chumakova

    (School of Mathematics and Maxwell Institute for Mathematical Sciences, The University of Edinburgh)

  • Natalia A. Bulgakova

    (Development and Neuroscience, and the Gurdon Institute, The University of Cambridge
    Present address: Department of Biomedical Science, The University of Sheffield, Sheffield S10 2TN, UK)

  • Nicholas H. Brown

    (Development and Neuroscience, and the Gurdon Institute, The University of Cambridge)

Abstract

Interphase microtubule organization is critical for cell function and tissue architecture. In general, physical mechanisms are sufficient to drive microtubule organization in single cells, whereas cells within tissues are thought to utilize signalling mechanisms. By improving the imaging and quantitation of microtubule alignment within developing Drosophila embryos, here we demonstrate that microtubule alignment underneath the apical surface of epithelial cells follows cell shape. During development, epidermal cell elongation and microtubule alignment occur simultaneously, but by perturbing cell shape, we discover that microtubule organization responds to cell shape, rather than the converse. A simple set of microtubule behaviour rules is sufficient for a computer model to mimic the observed responses to changes in cell surface geometry. Moreover, we show that microtubules colliding with cell boundaries zip-up or depolymerize in an angle-dependent manner, as predicted by the model. Finally, we show microtubule alignment responds to cell shape in diverse epithelia.

Suggested Citation

  • Juan Manuel Gomez & Lyubov Chumakova & Natalia A. Bulgakova & Nicholas H. Brown, 2016. "Microtubule organization is determined by the shape of epithelial cells," Nature Communications, Nature, vol. 7(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13172
    DOI: 10.1038/ncomms13172
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    Cited by:

    1. Amrita Singh & Sameedha Thale & Tobias Leibner & Lucas Lamparter & Andrea Ricker & Harald Nüsse & Jürgen Klingauf & Milos Galic & Mario Ohlberger & Maja Matis, 2024. "Dynamic interplay of microtubule and actomyosin forces drive tissue extension," Nature Communications, Nature, vol. 15(1), pages 1-14, December.

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