IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-41449-6.html
   My bibliography  Save this article

Hexanematic crossover in epithelial monolayers depends on cell adhesion and cell density

Author

Listed:
  • Julia Eckert

    (Universiteit Leiden
    The University of Queensland, St. Lucia)

  • Benoît Ladoux

    (Université Paris Cité, CNRS, Institut Jacques Monod)

  • René-Marc Mège

    (Université Paris Cité, CNRS, Institut Jacques Monod)

  • Luca Giomi

    (Universiteit Leiden)

  • Thomas Schmidt

    (Universiteit Leiden)

Abstract

Changes in tissue geometry during developmental processes are associated with collective migration of cells. Recent experimental and numerical results suggest that these changes could leverage on the coexistence of nematic and hexatic orientational order at different length scales. How this multiscale organization is affected by the material properties of the cells and their substrate is presently unknown. In this study, we address these questions in monolayers of Madin-Darby canine kidney cells having various cell densities and molecular repertoires. At small length scales, confluent monolayers are characterized by a prominent hexatic order, independent of the presence of E-cadherin, monolayer density, and underlying substrate stiffness. However, all three properties affect the meso-scale tissue organization. The length scale at which hexatic order transits to nematic order, the “hexanematic” crossover scale, strongly depends on cell-cell adhesions and correlates with monolayer density. Our study demonstrates how epithelial organization is affected by mechanical properties, and provides a robust description of tissue organization during developmental processes.

Suggested Citation

  • Julia Eckert & Benoît Ladoux & René-Marc Mège & Luca Giomi & Thomas Schmidt, 2023. "Hexanematic crossover in epithelial monolayers depends on cell adhesion and cell density," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41449-6
    DOI: 10.1038/s41467-023-41449-6
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-41449-6
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-41449-6?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Claire Bertet & Lawrence Sulak & Thomas Lecuit, 2004. "Myosin-dependent junction remodelling controls planar cell intercalation and axis elongation," Nature, Nature, vol. 429(6992), pages 667-671, June.
    2. Anaïs Bailles & Claudio Collinet & Jean-Marc Philippe & Pierre-François Lenne & Edwin Munro & Thomas Lecuit, 2019. "Genetic induction and mechanochemical propagation of a morphogenetic wave," Nature, Nature, vol. 572(7770), pages 467-473, August.
    3. Dong-Yuan Chen & Justin Crest & Sebastian J. Streichan & David Bilder, 2019. "Extracellular matrix stiffness cues junctional remodeling for 3D tissue elongation," Nature Communications, Nature, vol. 10(1), pages 1-15, December.
    4. Maureen Cetera & Guillermina R. Ramirez-San Juan & Patrick W. Oakes & Lindsay Lewellyn & Michael J. Fairchild & Guy Tanentzapf & Margaret L. Gardel & Sally Horne-Badovinac, 2014. "Epithelial rotation promotes the global alignment of contractile actin bundles during Drosophila egg chamber elongation," Nature Communications, Nature, vol. 5(1), pages 1-12, December.
    5. Kyogo Kawaguchi & Ryoichiro Kageyama & Masaki Sano, 2017. "Topological defects control collective dynamics in neural progenitor cell cultures," Nature, Nature, vol. 545(7654), pages 327-331, May.
    6. Thuan Beng Saw & Amin Doostmohammadi & Vincent Nier & Leyla Kocgozlu & Sumesh Thampi & Yusuke Toyama & Philippe Marcq & Chwee Teck Lim & Julia M. Yeomans & Benoit Ladoux, 2017. "Topological defects in epithelia govern cell death and extrusion," Nature, Nature, vol. 544(7649), pages 212-216, April.
    Full references (including those not matched with items on IDEAS)

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Mehrana R. Nejad & Liam J. Ruske & Molly McCord & Jun Zhang & Guanming Zhang & Jacob Notbohm & Julia M. Yeomans, 2024. "Stress-shape misalignment in confluent cell layers," Nature Communications, Nature, vol. 15(1), pages 1-8, December.

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Hannah J. Gustafson & Nikolas Claussen & Stefano Renzis & Sebastian J. Streichan, 2022. "Patterned mechanical feedback establishes a global myosin gradient," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Tom Brandstätter & David B. Brückner & Yu Long Han & Ricard Alert & Ming Guo & Chase P. Broedersz, 2023. "Curvature induces active velocity waves in rotating spherical tissues," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    3. Yingwei Wang & Qi Li & Jupeng Zhao & Jiamin Chen & Dongxue Wu & Youling Zheng & Jiaxin Wu & Jie Liu & Jianlong Lu & Jianhua Zhang & Zheng Wu, 2023. "Mechanically induced pyroptosis enhances cardiosphere oxidative stress resistance and metabolism for myocardial infarction therapy," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    4. Ariadna Marín-Llauradó & Sohan Kale & Adam Ouzeri & Tom Golde & Raimon Sunyer & Alejandro Torres-Sánchez & Ernest Latorre & Manuel Gómez-González & Pere Roca-Cusachs & Marino Arroyo & Xavier Trepat, 2023. "Mapping mechanical stress in curved epithelia of designed size and shape," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    5. Özge Özgüç & Ludmilla de Plater & Varun Kapoor & Anna Francesca Tortorelli & Andrew G Clark & Jean-Léon Maître, 2022. "Cortical softening elicits zygotic contractility during mouse preimplantation development," PLOS Biology, Public Library of Science, vol. 20(3), pages 1-23, March.
    6. Pragya Arora & Souvik Sadhukhan & Saroj Kumar Nandi & Dapeng Bi & A. K. Sood & Rajesh Ganapathy, 2024. "A shape-driven reentrant jamming transition in confluent monolayers of synthetic cell-mimics," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    7. Daniel Sánchez-Gutiérrez & Aurora Sáez & Alberto Pascual & Luis M Escudero, 2013. "Topological Progression in Proliferating Epithelia Is Driven by a Unique Variation in Polygon Distribution," PLOS ONE, Public Library of Science, vol. 8(11), pages 1-8, November.
    8. Claire Leclech & David Gonzalez-Rodriguez & Aurélien Villedieu & Thévy Lok & Anne-Marie Déplanche & Abdul I. Barakat, 2022. "Topography-induced large-scale antiparallel collective migration in vascular endothelium," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    9. Mehrana R. Nejad & Liam J. Ruske & Molly McCord & Jun Zhang & Guanming Zhang & Jacob Notbohm & Julia M. Yeomans, 2024. "Stress-shape misalignment in confluent cell layers," Nature Communications, Nature, vol. 15(1), pages 1-8, December.
    10. Stefan Harmansa & Alexander Erlich & Christophe Eloy & Giuseppe Zurlo & Thomas Lecuit, 2023. "Growth anisotropy of the extracellular matrix shapes a developing organ," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    11. Hiroyuki Uechi & Kazuki Fukushima & Ryota Shirasawa & Sayaka Sekine & Erina Kuranaga, 2022. "Inhibition of negative feedback for persistent epithelial cell–cell junction contraction by p21-activated kinase 3," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    12. Antonio Lamura & Adriano Tiribocchi, 2021. "Shearing Effects on the Phase Coarsening of Binary Mixtures Using the Active Model B," Mathematics, MDPI, vol. 9(23), pages 1-13, November.
    13. João Firmino & Jean-Yves Tinevez & Elisabeth Knust, 2013. "Crumbs Affects Protein Dynamics In Anterior Regions Of The Developing Drosophila Embryo," PLOS ONE, Public Library of Science, vol. 8(3), pages 1-10, March.
    14. Sanjay Karki & Mehdi Saadaoui & Valentin Dunsing & Stephen Kerridge & Elise Silva & Jean-Marc Philippe & Cédric Maurange & Thomas Lecuit, 2023. "Serotonin signaling regulates actomyosin contractility during morphogenesis in evolutionarily divergent lineages," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    15. Joanny, Jean-François & Indekeu, Joseph O., 2023. "Statistical physics of active matter, cell division and cell aggregation," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 631(C).
    16. Tomer Stern & Stanislav Y Shvartsman & Eric F Wieschaus, 2020. "Template-based mapping of dynamic motifs in tissue morphogenesis," PLOS Computational Biology, Public Library of Science, vol. 16(8), pages 1-20, August.
    17. Haruko Watanabe-Takano & Katsuhiro Kato & Eri Oguri-Nakamura & Tomohiro Ishii & Koji Kobayashi & Takahisa Murata & Koichiro Tsujikawa & Takaki Miyata & Yoshiaki Kubota & Yasuyuki Hanada & Koichi Nishi, 2024. "Endothelial cells regulate alveolar morphogenesis by constructing basement membranes acting as a scaffold for myofibroblasts," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
    18. Julien Fierling & Alphy John & Barthélémy Delorme & Alexandre Torzynski & Guy B. Blanchard & Claire M. Lye & Anna Popkova & Grégoire Malandain & Bénédicte Sanson & Jocelyn Étienne & Philippe Marmottan, 2022. "Embryo-scale epithelial buckling forms a propagating furrow that initiates gastrulation," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    19. Japinder Nijjer & Changhao Li & Qiuting Zhang & Haoran Lu & Sulin Zhang & Jing Yan, 2021. "Mechanical forces drive a reorientation cascade leading to biofilm self-patterning," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
    20. Chiao-Peng Hsu & Alfredo Sciortino & Yu Alice Trobe & Andreas R. Bausch, 2022. "Activity-induced polar patterns of filaments gliding on a sphere," Nature Communications, Nature, vol. 13(1), pages 1-8, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41449-6. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.