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  A fluid-to-solid jamming transition underlies vertebrate body axis elongation

Mongera, A., Gustafson, H., Rowghanian, P., Shelton, E., Kealhofer, D., Serwane, F., et al. (2018). A fluid-to-solid jamming transition underlies vertebrate body axis elongation. Nature, 561(7723), 401-405. doi:10.1038/s41586-018-0479-2.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0002-0A59-0 Version Permalink: http://hdl.handle.net/21.11116/0000-0002-FADC-D
Genre: Journal Article

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 Creators:
Mongera, A., Author
Gustafson, H., Author
Rowghanian, P., Author
Shelton, E., Author
Kealhofer, D., Author
Serwane, F.1, 2, Author              
Lucio, A., Author
Giammona, J., Author
Campas, O., Author
Affiliations:
1Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society, ou_2364731              
2Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany, ou_persistent22              

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 Abstract: Just as in clay moulding or glass blowing, physically sculpting biological structures requires the constituent material to locally flow like a fluid while maintaining overall mechanical integrity like a solid. Disordered soft materials, such as foams, emulsions and colloidal suspensions, switch from fluid-like to solid-like behaviours at a jamming transition1,2,3,4. Similarly, cell collectives have been shown to display glassy dynamics in 2D and 3D5,6 and jamming in cultured epithelial monolayers7,8, behaviours recently predicted theoretically9,10,11 and proposed to influence asthma pathobiology8 and tumour progression12. However, little is known about whether these seemingly universal behaviours occur in vivo13 and, specifically, whether they play any functional part during embryonic morphogenesis. Here, by combining direct in vivo measurements of tissue mechanics with analysis of cellular dynamics, we show that during vertebrate body axis elongation, posterior tissues undergo a jamming transition from a fluid-like behaviour at the extending end, the mesodermal progenitor zone, to a solid-like behaviour in the presomitic mesoderm. We uncover an anteroposterior, N-cadherin-dependent gradient in yield stress that provides increasing mechanical integrity to the presomitic mesoderm, consistent with the tissue transiting from a wetter to a dryer foam-like architecture. Our results show that cell-scale stresses fluctuate rapidly (within about 1 min), enabling cell rearrangements and effectively ‘melting’ the tissue at the growing end. Persistent (more than 0.5 h) stresses at supracellular scales, rather than cell-scale stresses, guide morphogenetic flows in fluid-like tissue regions. Unidirectional axis extension is sustained by the reported rigidification of the presomitic mesoderm, which mechanically supports posterior, fluid-like tissues during remodelling before their maturation. The spatiotemporal control of fluid-like and solid-like tissue states may represent a generic physical mechanism of embryonic morphogenesis.

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Language(s): eng - English
 Dates: 2017-09-082018-08-032018-09-052018-09-01
 Publication Status: Published in print
 Pages: 21
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 Table of Contents: -
 Rev. Type: Peer
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Title: Nature
  Abbreviation : Nature
Source Genre: Journal
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Publ. Info: London : Nature Publishing Group
Pages: - Volume / Issue: 561 (7723) Sequence Number: - Start / End Page: 401 - 405 Identifier: ISSN: 0028-0836
CoNE: https://pure.mpg.de/cone/journals/resource/954925427238