A fluid-to-solid jamming transition underlies vertebrate body axis elongation
Alessandro Mongera,
Payam Rowghanian,
Hannah J. Gustafson,
Elijah Shelton,
David A. Kealhofer,
Emmet K. Carn,
Friedhelm Serwane,
Adam A. Lucio,
James Giammona and
Otger Campàs ()
Additional contact information
Alessandro Mongera: University of California
Payam Rowghanian: University of California
Hannah J. Gustafson: University of California
Elijah Shelton: University of California
David A. Kealhofer: University of California
Emmet K. Carn: University of California
Friedhelm Serwane: University of California
Adam A. Lucio: University of California
James Giammona: University of California
Otger Campàs: University of California
Nature, 2018, vol. 561, issue 7723, 401-405
Abstract:
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 transition1–4. 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 theoretically9–11 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.
Keywords: Jamming Transition; Presomitic Mesoderm (PSM); Ferrofluid Droplets; Droplet Contour; Droplet Deformation (search for similar items in EconPapers)
Date: 2018
References: Add references at CitEc
Citations: View citations in EconPapers (4)
Downloads: (external link)
https://www.nature.com/articles/s41586-018-0479-2 Abstract (text/html)
Access to the full text of the articles in this series is restricted.
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:561:y:2018:i:7723:d:10.1038_s41586-018-0479-2
Ordering information: This journal article can be ordered from
https://www.nature.com/
DOI: 10.1038/s41586-018-0479-2
Access Statistics for this article
Nature is currently edited by Magdalena Skipper
More articles in Nature from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().