Active Fingering Instability in Tissue Spreading

Ricard Alert, Carles Blanch-Mercader, and Jaume Casademunt
Phys. Rev. Lett. 122, 088104 – Published 1 March 2019
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Abstract

During the spreading of epithelial tissues, the advancing tissue front often develops fingerlike protrusions. Their resemblance to traditional viscous fingering patterns in driven fluids suggests that epithelial fingers could arise from an interfacial instability. However, the existence and physical mechanism of such a putative instability remain unclear. Here, based on an active polar fluid model for epithelial spreading, we analytically predict a generic instability of the tissue front. On the one hand, active cellular traction forces impose a velocity gradient that leads to an accelerated front, which is, thus, unstable to long-wavelength perturbations. On the other hand, contractile intercellular stresses typically dominate over surface tension in stabilizing short-wavelength perturbations. Finally, the finite range of hydrodynamic interactions in the tissue selects a wavelength for the fingering pattern, which is, thus, given by the smallest between the tissue size and the hydrodynamic screening length. Overall, we show that spreading epithelia experience an active fingering instability based on a simple kinematic mechanism. Moreover, our results underscore the crucial role of long-range hydrodynamic interactions in the dynamics of tissue morphology.

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  • Received 28 February 2018

DOI:https://doi.org/10.1103/PhysRevLett.122.088104

© 2019 American Physical Society

Physics Subject Headings (PhySH)

Fluid DynamicsPhysics of Living Systems

Authors & Affiliations

Ricard Alert1,2,*, Carles Blanch-Mercader3,4, and Jaume Casademunt1,2

  • 1Departament de Física de la Matèria Condensada, Universitat de Barcelona, Avinguda Diagonal 647, 08028 Barcelona, Spain
  • 2Universitat de Barcelona Institute of Complex Systems (UBICS), Universitat de Barcelona, 08028 Barcelona, Spain
  • 3Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS, 26 rue d’Ulm, 75005 Paris, France
  • 4Department of Biochemistry, Faculty of Sciences, University of Geneva, 30, Quai Ernest-Ansermet, 1205 Genève, Switzerland

  • *Present address: Princeton Center for Theoretical Science and Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton NJ 08544, USA. ricard.alert@princeton.edu

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Issue

Vol. 122, Iss. 8 — 1 March 2019

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