Tissue cohesion and the mechanics of cell rearrangement

Morphogenetic processes often involve the rapid rearrangement of cells held together by mutual adhesion. The dynamic nature of this adhesion endows tissues with liquid-like properties, such that large-scale shape changes appear as tissue flows. Generally, the resistance to flow (tissue viscosity) is expected to depend on the cohesion of a tissue (how strongly its cells adhere to each other), but the exact relationship between these parameters is not known. Here, we analyse the link between cohesion and viscosity to uncover basic mechanical principles of cell rearrangement. We show that for vertebrate and invertebrate tissues, viscosity varies in proportion to cohesion over a 200-fold range of values. We demonstrate that this proportionality is predicted by a cell-based model of tissue viscosity. To do so, we analyse cell adhesion in Xenopus embryonic tissues and determine a number of parameters, including tissue surface tension (as a measure of cohesion), cell contact fluctuation and cortical tension. In the tissues studied, the ratio of surface tension to viscosity, which has the dimension of a velocity, is 1.8 µm/min. This characteristic velocity reflects the rate of cell-cell boundary contraction during rearrangement, and sets a limit to rearrangement rates. Moreover, we propose that, in these tissues, cell movement is maximally efficient. Our approach to cell rearrangement mechanics links adhesion to the resistance of a tissue to plastic deformation, identifies the characteristic velocity of the process, and provides a basis for the comparison of tissues with mechanical properties that may vary by orders of magnitude.

[1]  Siwei Zhang,et al.  ERK and phosphoinositide 3-kinase temporally coordinate different modes of actin-based motility during embryonic wound healing , 2013, Journal of Cell Science.

[2]  W. Blackwell HeLa cells , 1973, Molecular and Cellular Biochemistry.

[3]  J. Bereiter-Hahn,et al.  Hydrostatic pressure in epidermal cells is dependent on Ca-mediated contractions. , 1987, Journal of cell science.

[4]  T. Lecuit,et al.  Cell surface mechanics and the control of cell shape, tissue patterns and morphogenesis , 2007, Nature Reviews Molecular Cell Biology.

[5]  T. Naismith,et al.  Myosin-based cortical tension in Dictyostelium resolved into heavy and light chain-regulated components , 1996, Journal of Muscle Research and Cell Motility.

[6]  G. Bokoch Biology of the p21-activated kinases. , 2003, Annual review of biochemistry.

[7]  M. Koehl,et al.  The dorsal involuting marginal zone stiffens anisotropically during its convergent extension in the gastrula of Xenopus laevis. , 1995, Development.

[8]  Françoise Brochard-Wyart,et al.  Aspiration , 2019, Differential Diagnosis of Cardiopulmonary Disease.

[9]  W. Nelson,et al.  Localized zones of Rho and Rac activities drive initiation and expansion of epithelial cell–cell adhesion , 2007, The Journal of cell biology.

[10]  D. Weitz,et al.  Mechanical properties of Xenopus egg cytoplasmic extracts. , 2005, Biophysical journal.

[11]  Y. Sawada,et al.  Hydrodynamics and cell motion during the rounding of two dimensional hydra cell aggregates , 2002 .

[12]  R. Winklbauer Mesodermal cell migration during Xenopus gastrulation. , 1990, Developmental biology.

[13]  G. Forgacs,et al.  Viscoelastic properties of living embryonic tissues: a quantitative study. , 1998, Biophysical journal.

[14]  R. Winklbauer,et al.  PDGF-A controls mesoderm cell orientation and radial intercalation during Xenopus gastrulation , 2011, Development.

[15]  H. P. Ting-Beall,et al.  Myosin I contributes to the generation of resting cortical tension. , 1999, Biophysical journal.

[16]  A. Frangakis,et al.  The molecular architecture of cadherins in native epidermal desmosomes , 2007, Nature.

[17]  T. Takeuchi,et al.  [Entamoeba histolytica]. , 1999, Nihon rinsho. Japanese journal of clinical medicine.

[18]  Ana Rolo,et al.  Convergence and extension at gastrulation require a myosin IIB-dependent cortical actin network , 2008, Development.

[19]  Jeffrey R Morgan,et al.  Quantification of the forces driving self-assembly of three-dimensional microtissues , 2011, Proceedings of the National Academy of Sciences.

[20]  E. Sahai,et al.  Collective cell migration requires suppression of actomyosin at cell-cell contacts mediated by DDR1 and the cell polarity regulators Par3 and Par6 , 2010, Nature Cell Biology.

[21]  Tony J. C. Harris,et al.  The PAR complex regulates pulsed actomyosin contractions during amnioserosa apical constriction in Drosophila , 2010, Development.

[22]  G. S. Davis,et al.  Germ-layer surface tensions and "tissue affinities" in Rana pipiens gastrulae: quantitative measurements. , 1997, Developmental biology.

[23]  F. Fagotto,et al.  Cadherin-dependent differential cell adhesion in Xenopus causes cell sorting in vitro but not in the embryo , 2012, Journal of Cell Science.

[24]  M. Krieg,et al.  Tensile forces govern germ-layer organization in zebrafish , 2008, Nature Cell Biology.

[25]  A Wilhelm Neumann,et al.  Tissue surface tension measurement by rigorous axisymmetric drop shape analysis. , 2009, Colloids and surfaces. B, Biointerfaces.

[26]  James A. Spudich,et al.  Capping of surface receptors and concomitant cortical tension are generated by conventional myosin , 1989, Nature.

[27]  M. S. Steinberg,et al.  The differential adhesion hypothesis: a direct evaluation. , 2005, Developmental biology.

[28]  François Graner,et al.  The role of fluctuations and stress on the effective viscosity of cell aggregates , 2009, Proceedings of the National Academy of Sciences.

[29]  D. Leckband,et al.  Direct molecular force measurements of multiple adhesive interactions between cadherin ectodomains. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[30]  L. Sulak,et al.  Myosin-dependent junction remodelling controls planar cell intercalation and axis elongation , 2004, Nature.

[31]  Jean-Léon Maître,et al.  Adhesion Functions in Cell Sorting by Mechanically Coupling the Cortices of Adhering Cells , 2012, Science.

[32]  Marco Idiart,et al.  Rounding of aggregates of biological cells: Experiments and simulations , 2004, cond-mat/0411647.

[33]  R. Winklbauer,et al.  Antero-posterior tissue polarity links mesoderm convergent extension to axial patterning , 2004, Nature.

[34]  Françoise Brochard-Wyart,et al.  Mechanosensitive shivering of model tissues under controlled aspiration , 2011, Proceedings of the National Academy of Sciences.

[35]  R. Waugh,et al.  Rheological analysis and measurement of neutrophil indentation. , 2004, Biophysical journal.

[36]  D Needham,et al.  A sensitive measure of surface stress in the resting neutrophil. , 1992, Biophysical journal.

[37]  Frank Jülicher,et al.  Quantitative differences in tissue surface tension influence zebrafish germ layer positioning , 2008, HFSP journal.

[38]  D. Weaire,et al.  Soap, cells and statistics – random patterns in two dimensions , 1984 .

[39]  R. Winklbauer,et al.  Epithelial coating controls mesenchymal shape change through tissue-positioning effects and reduction of surface-minimizing tension , 2008, Nature Cell Biology.

[40]  Eric F. Wieschaus,et al.  Pulsed contractions of an actin–myosin network drive apical constriction , 2009, Nature.

[41]  Jaume Casademunt,et al.  Dynamical organization of the cytoskeletal cortex probed by micropipette aspiration , 2010, Proceedings of the National Academy of Sciences.

[42]  N S Goel,et al.  A rheological mechanism sufficient to explain the kinetics of cell sorting. , 1972, Journal of theoretical biology.

[43]  Martin Bergert,et al.  Cell mechanics control rapid transitions between blebs and lamellipodia during migration , 2012, Proceedings of the National Academy of Sciences.

[44]  Paul A. Janmey,et al.  Soft biological materials and their impact on cell function. , 2007, Soft matter.

[45]  G. Brodland,et al.  Cellular interfacial and surface tensions determined from aggregate compression tests using a finite element model , 2009, HFSP journal.

[46]  Lance A Davidson,et al.  Natural variation in embryo mechanics: gastrulation in Xenopus laevis is highly robust to variation in tissue stiffness , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.

[47]  M. Dembo,et al.  Baseline mechanical characterization of J774 macrophages. , 2009, Biophysical journal.

[48]  B. Gumbiner,et al.  Regulation of cadherin-mediated adhesion in morphogenesis , 2005, Nature Reviews Molecular Cell Biology.

[49]  B. Honig,et al.  Coaction of intercellular adhesion and cortical tension specifies tissue surface tension , 2010, Proceedings of the National Academy of Sciences.

[50]  J. Tinevez,et al.  Role of cortical tension in bleb growth , 2009, Proceedings of the National Academy of Sciences.

[51]  Pierre-François Lenne,et al.  Planar polarized actomyosin contractile flows control epithelial junction remodelling , 2010, Nature.

[52]  R. Winklbauer,et al.  Vegetal rotation, a new gastrulation movement involved in the internalization of the mesoderm and endoderm in Xenopus. , 1999, Development.

[53]  Asako Shindo,et al.  PCP and Septins Compartmentalize Cortical Actomyosin to Direct Collective Cell Movement , 2014, Science.

[54]  H. Schwarz,et al.  Electron microscopy of the amphibian model systems Xenopus laevis and Ambystoma mexicanum. , 2010, Methods in cell biology.

[55]  T. Bouwmeester,et al.  The role of paraxial protocadherin in selective adhesion and cell movements of the mesoderm during Xenopus gastrulation. , 1998, Development.

[56]  Jennifer A Zallen,et al.  Patterned gene expression directs bipolar planar polarity in Drosophila. , 2004, Developmental cell.

[57]  Daniel J. Muller,et al.  Hydrostatic pressure and the actomyosin cortex drive mitotic cell rounding , 2011, Nature.

[58]  Vladimir Mironov,et al.  Relating cell and tissue mechanics: Implications and applications , 2008, Developmental dynamics : an official publication of the American Association of Anatomists.

[59]  Kai Dierkes,et al.  Monitoring actin cortex thickness in live cells. , 2013, Biophysical journal.

[60]  B. Geiger,et al.  A functional test for maternally inherited cadherin in Xenopus shows its importance in cell adhesion at the blastula stage. , 1994, Development.

[61]  Olivia Luu,et al.  Large-scale mechanical properties of Xenopus embryonic epithelium , 2011, Proceedings of the National Academy of Sciences.

[62]  A. Jagota,et al.  The Role of Viscoelastic Adhesive Contact in the Sintering of Polymeric Particles. , 2001, Journal of colloid and interface science.

[63]  Lance A Davidson,et al.  Variation and robustness of the mechanics of gastrulation: the role of tissue mechanical properties during morphogenesis. , 2007, Birth defects research. Part C, Embryo today : reviews.

[64]  J. Rieu,et al.  Fine Tuning of Tissues' Viscosity and Surface Tension through Contractility Suggests a New Role for α-Catenin , 2013, PloS one.

[65]  Paul Skoglund,et al.  The forces that shape embryos: physical aspects of convergent extension by cell intercalation , 2008, Physical biology.

[66]  Río,et al.  Axisymmetric Drop Shape Analysis: Computational Methods for the Measurement of Interfacial Properties from the Shape and Dimensions of Pendant and Sessile Drops. , 1997, Journal of colloid and interface science.