Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

Mechanical regulation of early vertebrate embryogenesis

Abstract

Embryonic cells grow in environments that provide a plethora of physical cues, including mechanical forces that shape the development of the entire embryo. Despite their prevalence, the role of these forces in embryonic development and their integration with chemical signals have been mostly neglected, and scrutiny in modern molecular embryology tilted, instead, towards the dissection of molecular pathways involved in cell fate determination and patterning. It is now possible to investigate how mechanical signals induce downstream genetic regulatory networks to regulate key developmental processes in the embryo. Here, we review the insights into mechanical control of early vertebrate development, including the role of forces in tissue patterning and embryonic axis formation. We also highlight recent in vitro approaches using individual embryonic stem cells and self-organizing multicellular models of human embryos, which have been instrumental in expanding our understanding of how mechanics tune cell fate and cellular rearrangements during human embryonic development.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Forces acting in animal embryos.
Fig. 2: Mechanical regulation of cell fate.
Fig. 3: Force-induced symmetry breaking.
Fig. 4: Mechanics of cell rearrangements.
Fig. 5: Stem cell models of early mammalian development.
Fig. 6: Human gastruloids.

Similar content being viewed by others

References

  1. Howard, J., Grill, S. W. & Bois, J. S. Turing’s next steps: the mechanochemical basis of morphogenesis. Nat. Rev. Mol. Cell Biol. 12, 400–406 (2011). This review introduces the physical concepts necessary to understand mechanochemical patterning in developing embryos.

    Article  CAS  Google Scholar 

  2. Keller, R. Physical biology returns to morphogenesis. Science 338, 201–203 (2012).

    Article  CAS  PubMed  Google Scholar 

  3. Heisenberg, C. P. & Bellaïche, Y. Forces in tissue morphogenesis and patterning. Cell 153, 948 (2013).

    Article  CAS  PubMed  Google Scholar 

  4. Hashimoto, H. & Munro, E. Dynamic interplay of cell fate, polarity and force generation in ascidian embryos. Curr. Opin. Genet. Dev. 51, 67–77 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Munro, E., Robin, F. & Lemaire, P. Cellular morphogenesis in ascidians: how to shape a simple tadpole. Curr. Opin. Genet. Dev. 6, 399–405 (2006).

    Article  CAS  Google Scholar 

  6. Marston, D. J. & Goldstein, B. Actin-based forces driving embryonic morphogenesis in Caenorhabditis elegans. Curr. Opin. Genet. Dev. 16, 392–398 (2006).

    Article  CAS  PubMed  Google Scholar 

  7. Eaton, S. & Jülicher, F. Cell flow and tissue polarity patterns. Curr. Opin. Genet. Dev. 21, 747–752 (2011).

    Article  CAS  PubMed  Google Scholar 

  8. Quintin, S., Gally, C. & Labouesse, M. Epithelial morphogenesis in embryos: asymmetries, motors and brakes. Trends Genet. 24, 221–230 (2008).

    Article  CAS  PubMed  Google Scholar 

  9. Schwayer, C., Sikora, M., Slováková, J., Kardos, R. & Heisenberg, C.-P. Actin rings of power. Dev. Cell 37, 493–506 (2016).

    Article  CAS  PubMed  Google Scholar 

  10. Leptin, M. Gastrulation movements: the logic and the nuts and bolts. Dev. Cell 8, 305–320 (2005).

    Article  CAS  PubMed  Google Scholar 

  11. Lee, J.-Y. & Harland, R. M. Actomyosin contractility and microtubules drive apical constriction in Xenopus bottle cells. Dev. Biol. 311, 40–52 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Keller, R., Shook, D. & Skoglund, P. The forces that shape embryos: physical aspects of convergent extension by cell intercalation. Phys. Biol. 5, 015007 (2008).

    Article  PubMed  Google Scholar 

  13. Pfister, K., Shook, D. R., Chang, C., Keller, R. & Skoglund, P. Molecular model for force production and transmission during vertebrate gastrulation. Development 143, 715–727 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Maître, J. L. Mechanics of blastocyst morphogenesis. Biol. Cell 109, 323–338 (2017).

    Article  PubMed  Google Scholar 

  15. Fierro-González, J. C., White, M. D., Silva, J. C. & Plachta, N. Cadherin-dependent filopodia control preimplantation embryo compaction. Nat. Cell Biol. 15, 1424–1433 (2013).

    Article  PubMed  CAS  Google Scholar 

  16. Andreazzoli, M., Angeloni, D., Broccoli, V. & Demontis, G. C. Microgravity, stem cells, and embryonic development: challenges and opportunities for 3D tissue generation. Front. Astron. Space Sci. 4, 25 (2017).

    Article  Google Scholar 

  17. Porazinski, S. et al. YAP is essential for tissue tension to ensure vertebrate 3D body shape. Nature 521, 217–221 (2015). This work presents the link between YAP/TAZ regulation and shape control in a vertebrate embryo.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Saadaoui, M., Rocancourt, D., Roussel, J., Corson, F. & Gros, J. A tensile ring drives tissue flows to shape the gastrulating amniote embryo. Science 367, 453–458 (2020). This work introduces a force/structure model to predict the epiblast rearrangements during chick gastrulation.

    Article  CAS  PubMed  Google Scholar 

  19. Shellard, A., Szabó, A., Trepat, X. & Mayor, R. Supracellular contraction at the rear of neural crest cell groups drives collective chemotaxis. Science 362, 339–343 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Shook, D. R., Kasprowicz, E. M., Davidson, L. A. & Keller, R. Large, long range tensile forces drive convergence during Xenopus blastopore closure and body axis elongation. eLife 7, e26944 (2018). This work isolates the contribution of two specific morphogenetic processes (convergent extension and convergent thickening) in X. laevis gastrulation by performing macroscopic force measurements in explants.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Behrndt, M. et al. Forces driving epithelial spreading in zebrafish gastrulation. Science 338, 257–260 (2012).

    Article  CAS  PubMed  Google Scholar 

  22. Paré, A. C. & Zallen, J. A. Cellular, molecular, and biophysical control of epithelial cell intercalation. Curr. Top. Dev. Biol. 136, 167–193 (2020).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. Fernandez-Gonzalez, R., Simoes, S., de, M., Röper, J. C., Eaton, S. & Zallen, J. A. Myosin II dynamics are regulated by tension in intercalating cells. Dev. Cell 17, 736–743 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Luo, T., Mohan, K., Iglesias, P. A. & Robinson, D. N. Molecular mechanisms of cellular mechanosensing. Nat. Mater. 12, 1064–1071 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Dumortier, J. G. et al. Hydraulic fracturing and active coarsening position the lumen of the mouse blastocyst. Science 365, 465–468 (2019).

    Article  CAS  PubMed  Google Scholar 

  26. Chan, C. J. et al. Hydraulic control of mammalian embryo size and cell fate. Nature 571, 112–116 (2019).

    Article  CAS  PubMed  Google Scholar 

  27. Sutherland, A., Keller, R. & Lesko, A. Convergent extension in mammalian morphogenesis. Semin. Cell Dev. Biol. 100, 199–211 (2020).

    Article  CAS  PubMed  Google Scholar 

  28. Beloussov, L. V., Louchinskaia, N. N. & Stein, A. A. Tension-dependent collective cell movements in the early gastrula ectoderm of Xenopus laevis embryos. Dev. Genes Evol. 210, 92–104 (2000).

    Article  CAS  PubMed  Google Scholar 

  29. Shellard, A. & Mayor, R. Durotaxis: the hard path from in vitro to in vivo. Dev. Cell 56, 227–239 (2021).

    Article  CAS  PubMed  Google Scholar 

  30. Petridou, N. I. & Heisenberg, C. Tissue rheology in embryonic organization. EMBO J. 38, e102497 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Morita, H. et al. The physical basis of coordinated tissue spreading in zebrafish gastrulation. Dev. Cell 40, 354–366.e4 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Mongera, A. et al. A fluid-to-solid jamming transition underlies vertebrate body axis elongation. Nature 561, 401–405 (2018). This work proposes to describe zebrafish axis elongation using a jamming–unjamming transition, with physical measurements of the stress in the tissue.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Pérez-González, C. et al. Active wetting of epithelial tissues. Nat. Phys. 15, 79–88 (2019).

    Article  PubMed  CAS  Google Scholar 

  34. Wallmeyer, B., Trinschek, S., Yigit, S., Thiele, U. & Betz, T. Collective cell migration in embryogenesis follows the laws of wetting. Biophys. J. 114, 213–222 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Petridou, N. I., Corominas-Murtra, B., Heisenberg, C. P. & Hannezo, E. Rigidity percolation uncovers a structural basis for embryonic tissue phase transitions. Cell 184, 1914–1928.e19 (2021).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Stern, C. D. Gastrulation: From Cells to Embryo (Cold Spring Harbor Laboratory Press, 2004).

  37. Collinet, C. & Lecuit, T. Programmed and self-organized flow of information during morphogenesis. Nat. Rev. Mol. Cell Biol. 22, 245–265 (2021). This work presents a conceptual framework — morphogenetic information — that combines genetic, biochemical and mechanical cues.

    Article  CAS  PubMed  Google Scholar 

  38. Turing, A. The chemical basis of morphogenesis. Proc. R. Soc. Lond. B Biol. Sci. 237, 37–72 (1952).

    Google Scholar 

  39. Harris, A. K., Warner, P. & Stopak, D. Generation of spatially periodic patterns by a mechanical instability: a mechanical alternative to the Turing model. J. Embryol. Exp. Morphol. 1–20 (1984).

  40. Oster, G. F., Murray, J. D. & Harris, A. K. Mechanical aspects of mesenchymal morphogenesis. J. Embryol. Exp. Morphol. 78, 83–125 (1983).

    CAS  PubMed  Google Scholar 

  41. Goehring, N. W. & Grill, S. W. Cell polarity: mechanochemical patterning. Trends Cell Biol. 23, 72–80 (2013).

    Article  CAS  PubMed  Google Scholar 

  42. Shyer, A. E., Huycke, T. R., Lee, C., Mahadevan, L. & Tabin, C. J. Bending gradients: how the intestinal stem cell gets its home. Cell 161, 569–580 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Shyer, A. E. et al. Emergent cellular self-organization and mechanosensation initiate follicle pattern in the avian skin. Science 357, 811–815 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Farge, E. Mechanical induction of Twist in the Drosophila foregut/stomodeal primordium. Curr. Biol. 13, 1365–1377 (2003).

    Article  CAS  PubMed  Google Scholar 

  45. Desprat, N., Supatto, W., Pouille, P.-A., Beaurepaire, E. & Farge, E. Tissue deformation modulates Twist expression to determine anterior midgut differentiation in Drosophila embryos. Dev. Cell 15, 470–477 (2008).

    Article  CAS  PubMed  Google Scholar 

  46. Brunet, T. et al. Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria. Nat. Commun. 4, 1–15 (2013).

    Article  CAS  Google Scholar 

  47. Röper, J.-C. et al. The major β-catenin/E-cadherin junctional binding site is a primary molecular mechano-transductor of differentiation in vivo. eLife 7, e33381 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  48. Przybyla, L., Lakins, J. N. & Weaver, V. M. Tissue mechanics orchestrate Wnt-dependent human embryonic stem cell differentiation. Cell Stem Cell 19, 462–475 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Muncie, J. M. et al. Mechanical tension promotes formation of gastrulation-like nodes and patterns mesoderm specification in human embryonic stem cells. Dev. Cell 55, 679–694 (2020). This work studies mechanical patterning in stem cell colonies upon mesendoderm induction.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Niehrs, C. The complex world of WNT receptor signalling. Nat. Rev. Mol. Cell Biol. 13, 767–779 (2012).

    Article  CAS  PubMed  Google Scholar 

  51. Wallingford, J. B. et al. Dishevelled controls cell polarity during Xenopus gastrulation. Nature 405, 81–85 (2000).

    Article  CAS  PubMed  Google Scholar 

  52. Heisenberg, C.-P. et al. Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation. Nature 405, 76–81 (2000).

    Article  CAS  PubMed  Google Scholar 

  53. Sokol, S. Y. Spatial and temporal aspects of Wnt signaling and planar cell polarity during vertebrate embryonic development. Semin. Cell Dev. Biol. 42, 78–85 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Devenport, D. The cell biology of planar cell polarity. J. Cell Biol. 207, 171–179 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Chien, Y. H., Keller, R., Kintner, C. & Shook, D. R. Mechanical strain determines the axis of planar polarity in ciliated epithelia. Curr. Biol. 25, 2774–2784 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Aw, W. Y., Heck, B. W., Joyce, B. & Devenport, D. Transient tissue-scale deformation coordinates alignment of planar cell polarity junctions in the mammalian skin. Curr. Biol. 26, 2090–2100 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  57. Aigouy, B. et al. Cell flow reorients the axis of planar polarity in the wing epithelium of Drosophila. Cell 142, 773–786 (2010).

    Article  CAS  PubMed  Google Scholar 

  58. Mitchell, B. et al. The PCP pathway instructs the planar orientation of ciliated cells in the Xenopus larval skin. Curr. Biol. 19, 924–929 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Guirao, B. et al. Coupling between hydrodynamic forces and planar cell polarity orients mammalian motile cilia. Nat. Cell Biol. 12, 341–350 (2010).

    Article  CAS  PubMed  Google Scholar 

  60. Butler, M. T. & Wallingford, J. B. Planar cell polarity in development and disease. Nat. Rev. Mol. Cell Biol. 18, 375–388 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  61. Piccolo, S., Dupont, S. & Cordenonsi, M. The biology of YAP/TAZ: Hippo signaling and beyond. Physiol. Rev. 94, 1287–1312 (2014).

    Article  CAS  PubMed  Google Scholar 

  62. Tsai, B. P., Hoverter, N. P. & Waterman, M. L. Blending Hippo and WNT: sharing messengers and regulation. Cell 151, 1401–1403 (2012).

    Article  CAS  PubMed  Google Scholar 

  63. Dupont, S. et al. Role of YAP/TAZ in mechanotransduction. Nature 474, 179–183 (2011).

    Article  CAS  PubMed  Google Scholar 

  64. Halder, G., Dupont, S. & Piccolo, S. Transduction of mechanical and cytoskeletal cues by YAP and TAZ. Nat. Rev. Mol. Cell Biol. 13, 591–600 (2012).

    Article  CAS  PubMed  Google Scholar 

  65. Fernández, B. G. et al. Actin-capping protein and the Hippo pathway regulate F-actin and tissue growth in Drosophila. Development 138, 2337–2346 (2011).

    Article  PubMed  CAS  Google Scholar 

  66. Sansores-Garcia, L. et al. Modulating F-actin organization induces organ growth by affecting the Hippo pathway. EMBO J. 30, 2325–2335 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Rauskolb, C., Sun, S., Sun, G., Pan, Y. & Irvine, K. D. Cytoskeletal tension inhibits Hippo signaling through an Ajuba–Warts complex. Cell 158, 143–156 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Mateus, R. et al. Control of tissue growth by Yap relies on cell density and F-actin in zebrafish fin regeneration. Development 142, 2752–2763 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  69. Dong, J. et al. Elucidation of a universal size-control mechanism in Drosophila and mammals. Cell 130, 1120–1133 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  70. Heallen, T. et al. Hippo pathway inhibits Wnt signaling to restrain cardiomyocyte proliferation and heart size. Science 332, 458–461 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  71. Shraiman, B. I. Mechanical feedback as a possible regulator of tissue growth. Proc. Natl Acad. Sci. USA 102, 3318–3323 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  72. Irvine, K. D. & Shraiman, B. I. Mechanical control of growth: ideas, facts and challenges. Development 144, 4238–4248 (2017). This work introduces a conceptual framework to understand how a molecular relay can integrate growth and size control at the tissue and organismal level.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  73. Pan, Y., Heemskerk, I., Ibar, C., Shraiman, B. I. & Irvine, K. D. Differential growth triggers mechanical feedback that elevates Hippo signaling. Proc. Natl Acad. Sci. USA 113, E6974–E6983 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  74. Vining, K. H. & Mooney, D. J. Mechanical forces direct stem cell behaviour in development and regeneration. Nat. Rev. Mol. Cell Biol. 18, 728–742 (2017). This work reviews the mechanobiology of stem cells.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Elosegui-Artola, A. et al. Force triggers YAP nuclear entry by regulating transport across nuclear pores. Cell 171, 1397–1410.e14 (2017).

    Article  CAS  PubMed  Google Scholar 

  76. Tee, Y. H. et al. Cellular chirality arising from the self-organization of the actin cytoskeleton. Nat. Cell Biol. 17, 445–457 (2015).

    Article  CAS  PubMed  Google Scholar 

  77. Weaver, C. & Kimelman, D. Move it or lose it: axis specification in Xenopus. Development 131, 3491–3499 (2004).

    Article  CAS  PubMed  Google Scholar 

  78. Vincent, J.-P., Scharf, S. R. & Gerhart, J. C. Subcortical rotation in Xenopus eggs: a preliminary study of its mechanochemical basis. Cell Motil. Cytoskeleton 8, 143–154 (1987).

    Article  CAS  PubMed  Google Scholar 

  79. Black, S. D. & Gerhart, J. C. Experimental control of the site of embryonic axis formation in Xenopus laevis eggs centrifuged before first cleavage. Dev. Biol. 108, 310–324 (1985).

    Article  CAS  PubMed  Google Scholar 

  80. Waddington, C. H. Experiments on the development of chick and duck embryos, cultivated in vitro. Philos. Trans. R. Soc. London. Ser. B 221, 179–230 (1932).

    Article  Google Scholar 

  81. Coutelis, J., González-Morales, N., Géminard, C. & Noselli, S. Diversity and convergence in the mechanisms establishing L/R asymmetry in metazoa. EMBO Rep. 15, 926–937 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  82. Okada, Y. et al. Abnormal nodal flow precedes situs inversus in iv and inv mice. Mol. Cell 4, 459–468 (1999).

    Article  CAS  PubMed  Google Scholar 

  83. Nonaka, S. et al. Randomization of left–right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein. Cell 95, 829–837 (1998).

    Article  CAS  PubMed  Google Scholar 

  84. Hashimoto, M. et al. Planar polarization of node cells determines the rotational axis of node cilia. Nat. Cell Biol. 12, 170–176 (2010).

    Article  CAS  PubMed  Google Scholar 

  85. Song, H. et al. Planar cell polarity breaks bilateral symmetry by controlling ciliary positioning. Nature 466, 378–382 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  86. Maisonneuve, C. et al. Bicaudal C, a novel regulator of Dvl signaling abutting RNA-processing bodies, controls cilia orientation and leftward flow. Development 136, 3019–3030 (2009).

    Article  CAS  PubMed  Google Scholar 

  87. Shinohara, K. & Hamada, H. Cilia in left–right symmetry breaking. Cold Spring Harb. Perspect. Biol. 9, a028282 (2017).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  88. Tanaka, Y., Okada, Y. & Hirokawa, N. FGF-induced vesicular release of Sonic hedgehog and retinoic acid in leftward nodal flow is critical for left–right determination. Nature 435, 172–177 (2005).

    Article  CAS  PubMed  Google Scholar 

  89. Kawasumi, A. et al. Left–right asymmetry in the level of active Nodal protein produced in the node is translated into left–right asymmetry in the lateral plate of mouse embryos. Dev. Biol. 353, 321–330 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  90. Field, S. et al. Pkd1l1 establishes left–right asymmetry and physically interacts with Pkd2. Development 138, 1131–1142 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  91. Grimes, D. T. Making and breaking symmetry in development, growth and disease. Development 146, dev170985 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  92. Vandenberg, L. N. & Levin, M. A unified model for left–right asymmetry? Comparison and synthesis of molecular models of embryonic laterality. Dev. Biol. 379, 1–15 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Fukumoto, T., Kema, I. P. & Levin, M. Serotonin signaling is a very early step in patterning of the left–right axis in chick and frog embryos. Curr. Biol. 15, 794–803 (2005).

    Article  CAS  PubMed  Google Scholar 

  94. Adams, D. S. et al. Early, H+-V-ATPase-dependent proton flux is necessary for consistent left–right patterning of non-mammalian vertebrates. Development 133, 1657–1671 (2006).

    Article  CAS  PubMed  Google Scholar 

  95. Ziomek, C. A. & Johnson, M. H. Cell surface interaction induces polarization of mouse 8-cell blastomeres at compaction. Cell 21, 935–942 (1980).

    Article  CAS  PubMed  Google Scholar 

  96. Lorthongpanich, C. et al. Developmental fate and lineage commitment of singled mouse blastomeres. Development 139, 3722–3731 (2012).

    Article  CAS  PubMed  Google Scholar 

  97. Frum, T. & Ralston, A. Cell signaling and transcription factors regulating cell fate during formation of the mouse blastocyst. Trends Genet. 31, 402–410 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  98. Wicklow, E. et al. HIPPO pathway members restrict SOX2 to the inner cell mass where it promotes ICM fates in the mouse blastocyst. PLoS Genet. 10, e1004618 (2014).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  99. Bruce, A. E. E. & Heisenberg, C. P. Mechanisms of zebrafish epiboly: a current view. Curr. Top. Dev. Biol. 136, 319–341 (2020).

    Article  CAS  PubMed  Google Scholar 

  100. Solnica-Krezel, L. Conserved patterns of cell movements during vertebrate gastrulation. Curr. Biol. 15, R213–R228 (2005).

    Article  CAS  PubMed  Google Scholar 

  101. Sandersius, S. A., Chuai, M., Weijer, C. J. & Newman, T. J. A “chemotactic dipole” mechanism for large-scale vortex motion during primitive streak formation in the chick embryo. Phys. Biol. 8, 045008 (2011).

    Article  CAS  PubMed  Google Scholar 

  102. Winklbauer, R. & Parent, S. E. Forces driving cell sorting in the amphibian embryo. Mech. Dev. 144, 81–91 (2017).

    Article  CAS  PubMed  Google Scholar 

  103. Steinberg, M. S. Differential adhesion in morphogenesis: a modern view. Curr. Opin. Genet. Dev. 17, 281–286 (2007).

    Article  CAS  PubMed  Google Scholar 

  104. Duguay, D., Foty, R. A. & Steinberg, M. S. Cadherin-mediated cell adhesion and tissue segregation: qualitative and quantitative determinants. Dev. Biol. 253, 309–323 (2003).

    Article  CAS  PubMed  Google Scholar 

  105. Kania, A. & Klein, R. Mechanisms of ephrin–Eph signalling in development, physiology and disease. Nat. Rev. Mol. Cell Biol. 17, 240–256 (2016).

    Article  CAS  PubMed  Google Scholar 

  106. Cooke, J. E. & Moens, C. B. Boundary formation in the hindbrain: Eph only it were simple … Trends Neurosci. 25, 260–267 (2002).

    Article  CAS  PubMed  Google Scholar 

  107. Ninomiya, H. et al. Cadherin-dependent differential cell adhesion in Xenopus causes cell sorting in vitro but not in the embryo. J. Cell Sci. 125, 1877–1883 (2012).

    CAS  PubMed  Google Scholar 

  108. Canty, L., Zarour, E., Kashkooli, L., François, P. & Fagotto, F. Sorting at embryonic boundaries requires high heterotypic interfacial tension. Nat. Commun. 8, 157 (2017).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  109. Harris, A. K. Is cell sorting caused by differences in the work of intercellular adhesion? A critique of the Steinberg hypothesis. J. Theor. Biol. 61, 267–285 (1976).

    Article  CAS  PubMed  Google Scholar 

  110. Krieg, M. et al. Tensile forces govern germ-layer organization in zebrafish. Nat. Cell Biol. 10, 429–436 (2008).

    Article  CAS  PubMed  Google Scholar 

  111. Oates, A. C. et al. An early developmental role for Eph–ephrin interaction during vertebrate gastrulation. Mech. Dev. 83, 77–94 (1999).

    Article  CAS  PubMed  Google Scholar 

  112. Lecuit, T. & Lenne, P. F. Cell surface mechanics and the control of cell shape, tissue patterns and morphogenesis. Nat. Rev. Mol. Cell Biol. 8, 633–644 (2007).

    Article  CAS  PubMed  Google Scholar 

  113. Davis, G. S., Phillips, H. M. & Steinberg, M. S. Germ-layer surface tensions and “tissue affinities” in Rana pipiens gastrulae: quantitative measurements. Dev. Biol. 192, 630–644 (1997).

    Article  CAS  PubMed  Google Scholar 

  114. Campàs, O. et al. Quantifying cell-generated mechanical forces within living embryonic tissues. Nat. Methods 11, 183–189 (2014).

    Article  PubMed  CAS  Google Scholar 

  115. Schauer, A., Pinheiro, D., Hauschild, R. & Heisenberg, C. P. Zebrafish embryonic explants undergo genetically encoded self-assembly. eLife 9, e55190 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  116. Fulton, T. et al. Axis specification in zebrafish is robust to cell mixing and reveals a regulation of pattern formation by morphogenesis. Curr. Biol. 30, 2984–2994.e3 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  117. Torres-Paz, J. & Rétaux, S. Pescoids and chimeras to probe early evo-devo in the fish Astyanax mexicanus. Front. Cell Dev. Biol. 9, 927 (2021).

    Article  Google Scholar 

  118. Odell, G. M., Oster, G., Alberch, P. & Burnside, B. The mechanical basis of morphogenesis. I. Epithelial folding and invagination. Dev. Biol. 85, 446–462 (1981).

    Article  CAS  PubMed  Google Scholar 

  119. New, D. A. T. & Stein, K. F. Cultivation of mouse embryos in vitro. Nature 199, 297–299 (1963).

    Article  CAS  PubMed  Google Scholar 

  120. New, D. A. T. Development of explanted rat embryos in circulating medium. Development 17, 513–525 (1967).

    Article  CAS  Google Scholar 

  121. New, D. A. T., Coppola, P. T. & Terry, S. Culture of explanted rat embryos in rotating tubes. J. Reprod. Fertil. 35, 135–138 (1973).

    Article  CAS  PubMed  Google Scholar 

  122. Bedzhov, I. & Zernicka-Goetz, M. Self-organizing properties of mouse pluripotent cells initiate morphogenesis upon implantation. Cell 156, 1032–1044 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  123. Huang, Q. et al. Intravital imaging of mouse embryos. Science 368, 181–186 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  124. Aguilera-Castrejon, A. et al. Ex utero mouse embryogenesis from pre-gastrulation to late organogenesis. Nature 593, 119–124 (2021).

    Article  CAS  PubMed  Google Scholar 

  125. Engler, A. J., Sen, S., Sweeney, H. L. & Discher, D. E. Matrix elasticity directs stem cell lineage specification. Cell 126, 677–689 (2006).

    Article  CAS  PubMed  Google Scholar 

  126. Chaudhuri, O. et al. Hydrogels with tunable stress relaxation regulate stem cell fate and activity. Nat. Mater. 15, 326–334 (2016).

    Article  CAS  PubMed  Google Scholar 

  127. Xue, X. et al. Mechanics-guided embryonic patterning of neuroectoderm tissue from human pluripotent stem cells. Nat. Mater. 17, 633–641 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  128. Pathak, M. M. et al. Stretch-activated ion channel Piezo1 directs lineage choice in human neural stem cells. Proc. Natl Acad. Sci. USA 111, 16148–16153 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  129. Barzegari, A. et al. The role of Hippo signaling pathway and mechanotransduction in tuning embryoid body formation and differentiation. J. Cell. Physiol. 235, 5072–5083 (2020).

    Article  CAS  PubMed  Google Scholar 

  130. Slusarski, D. C. & Pelegri, F. Calcium signaling in vertebrate embryonic patterning and morphogenesis. Dev. Biol. 307, 1–13 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  131. Giorgi, C., Danese, A., Missiroli, S., Patergnani, S. & Pinton, P. Calcium dynamics as a machine for decoding signals. Trends Cell Biol. 28, 258–273 (2018).

    Article  CAS  PubMed  Google Scholar 

  132. Mitchel, J. A. et al. In primary airway epithelial cells, the unjamming transition is distinct from the epithelial-to-mesenchymal transition. Nat. Commun. 11, 5053 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  133. Trepat, X. et al. Viscoelasticity of human alveolar epithelial cells subjected to stretch. Am. J. Physiol. Lung Cell. Mol. Physiol. 287, L1025–L1034 (2004).

    Article  CAS  PubMed  Google Scholar 

  134. Casares, L. et al. Hydraulic fracture during epithelial stretching. Nat. Mater. 14, 343–351 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  135. Guo, M. et al. Cell volume change through water efflux impacts cell stiffness and stem cell fate. Proc. Natl Acad. Sci. USA 114, E8618–E8627 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  136. Warmflash, A., Sorre, B., Etoc, F., Siggia, E. D. & Brivanlou, A. H. A method to recapitulate early embryonic spatial patterning in human embryonic stem cells. Nat. Methods 11, 847–854 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  137. Eiraku, M. et al. Self-organizing optic-cup morphogenesis in three-dimensional culture. Nature 472, 51–56 (2011). This work presents mechanical patterning during organogenesis in a stem cell-based model.

    Article  CAS  PubMed  Google Scholar 

  138. Okuda, S. et al. Strain-triggered mechanical feedback in self-organizing optic-cup morphogenesis. Sci. Adv. 4, 1354 (2018).

    Article  CAS  Google Scholar 

  139. Simunovic, M. & Brivanlou, A. H. Embryoids, organoids and gastruloids: new approaches to understanding embryogenesis. Development 144, 976–985 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  140. Morgani, S. M., Metzger, J. J., Nichols, J., Siggia, E. D. & Hadjantonakis, A. K. Micropattern differentiation of mouse pluripotent stem cells recapitulates embryo regionalized cell fate patterning. eLife 7, e32839 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  141. Moris, N. et al. An in vitro model of early anteroposterior organization during human development. Nature 582, 410–415 (2020).

    Article  CAS  PubMed  Google Scholar 

  142. Sozen, B. et al. Self-assembly of embryonic and two extra-embryonic stem cell types into gastrulating embryo-like structures. Nat. Cell Biol. 20, 979–989 (2018).

    Article  CAS  PubMed  Google Scholar 

  143. Deglincerti, A., Etoc, F., Ozair, M. Z. & Brivanlou, A. H. Self-organization of spatial patterning in human embryonic stem cells. Curr. Top. Dev. Biol. 116, 99–113 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  144. Shahbazi, M. N. et al. Self-organization of the human embryo in the absence of maternal tissues. Nat. Cell Biol. 18, 700–708 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  145. Niu, Y. et al. Dissecting primate early post-implantation development using long-term in vitro embryo culture. Science 366, eaaw5754 (2019).

    Article  CAS  PubMed  Google Scholar 

  146. Ma, H. et al. In vitro culture of cynomolgus monkey embryos beyond early gastrulation. Science 366, eaax7890 (2019).

    Article  CAS  PubMed  Google Scholar 

  147. Shahbazi, M. N. Mechanisms of human embryo development: from cell fate to tissue shape and back. Development 147, dev190629 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  148. Vianello, S. & Lutolf, M. P. Understanding the mechanobiology of early mammalian development through bioengineered models. Dev. Cell 48, 751–763 (2019). This work reviews the bioengineering efforts dedicated to assess mechano-transduction in stem cell models.

    Article  CAS  PubMed  Google Scholar 

  149. Metzger, J. J., Simunovic, M. & Brivanlou, A. H. Synthetic embryology: controlling geometry to model early mammalian development. Curr. Opin. Genet. Dev. 52, 86–91 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  150. Rossant, J. Mouse and human blastocyst-derived stem cells: vive les differences. Development 142, 9–12 (2015).

    Article  CAS  PubMed  Google Scholar 

  151. Martyn, I., Brivanlou, A. H. & Siggia, E. D. A wave of WNT signaling balanced by secreted inhibitors controls primitive streak formation in micropattern colonies of human embryonic stem cells. Development 146, dev172791 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  152. Martyn, I., Siggia, E. D. & Brivanlou, A. H. Mapping cell migrations and fates in a gastruloid model to the human primitive streak. Development 146, dev179564 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  153. Simunovic, M. et al. A 3D model of a human epiblast reveals BMP4-driven symmetry breaking. Nat. Cell Biol. 21, 900–910 (2019).

    Article  CAS  PubMed  Google Scholar 

  154. van den Brink, S. C. et al. Single-cell and spatial transcriptomics reveal somitogenesis in gastruloids. Nature 582, 405–409 (2020).

    Article  PubMed  CAS  Google Scholar 

  155. Pukhlyakova, E., Aman, A. J., Elsayad, K. & Technau, U. β-Catenin-dependent mechanotransduction dates back to the common ancestor of Cnidaria and Bilateria. Proc. Natl Acad. Sci. USA 115, 6231–6236 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  156. Zheng, Y. et al. Controlled modelling of human epiblast and amnion development using stem cells. Nature 573, 421–425 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  157. Rivron, N. C. et al. Blastocyst-like structures generated solely from stem cells. Nature 557, 106–111 (2018).

    Article  CAS  PubMed  Google Scholar 

  158. Zhu, M. & Zernicka-Goetz, M. Principles of self-organization of the mammalian embryo. Cell 183, 1467–1478 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  159. Girgin, M. U. et al. Bioengineered embryoids mimic post-implantation development in vitro. Nat. Commun. 12, 5140 (2021).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  160. Gao, X. et al. Establishment of porcine and human expanded potential stem cells. Nat. Cell Biol. 21, 687–699 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  161. Linneberg-Agerholm, M. et al. Naïve human pluripotent stem cells respond to Wnt, Nodal, and LIF signalling to produce expandable naïve extra-embryonic endoderm. Development 146, dev180620 (2019).

    Article  CAS  PubMed  Google Scholar 

  162. Yu, L. et al. Blastocyst-like structures generated from human pluripotent stem cells. Nature 591, 620–626 (2021).

    Article  CAS  PubMed  Google Scholar 

  163. Liu, X. et al. Modelling human blastocysts by reprogramming fibroblasts into iBlastoids. Nature 591, 627–632 (2021).

    Article  CAS  PubMed  Google Scholar 

  164. Sozen, B. et al. Reconstructing aspects of human embryogenesis with pluripotent stem cells. Nat. Commun. 12, 1–13 (2021).

    Article  Google Scholar 

  165. Lemon, W. C. & McDole, K. Live-cell imaging in the era of too many microscopes. Curr. Opin. Cell Biol. 66, 34–42 (2020).

    Article  CAS  PubMed  Google Scholar 

  166. McDole, K. et al. In toto imaging and reconstruction of post-implantation mouse development at the single-cell level. Cell 175, 859–876.e33 (2018).

    Article  CAS  PubMed  Google Scholar 

  167. Kirby, T. J. & Lammerding, J. Emerging views of the nucleus as a cellular mechanosensor. Nat. Cell Biol. 20, 373–381 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  168. Doss, B. L. et al. Cell response to substrate rigidity is regulated by active and passive cytoskeletal stress. Proc. Natl Acad. Sci. USA 117, 12817–12825 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  169. Delmas, P. & Coste, B. XMechano-gated ion channels in sensory systems. Cell 155, 278–284 (2013).

    Article  CAS  PubMed  Google Scholar 

  170. Coste, B. et al. Piezo1 and Piezo2 are essential components of distinct mechanically activated cation channels. Science 330, 55–60 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  171. Korotkevich, E. et al. The apical domain is required and sufficient for the first lineage segregation in the mouse embryo. Dev. Cell 40, 235–247.e7 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  172. Hirate, Y. et al. Polarity-dependent distribution of angiomotin localizes hippo signaling in preimplantation embryos. Curr. Biol. 23, 1181–1194 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  173. Amadei, G. et al. Inducible stem-cell-derived embryos capture mouse morphogenetic events in vitro. Dev. Cell 56, 366–382 (2021).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  174. Campàs, O. A toolbox to explore the mechanics of living embryonic tissues. Semin. Cell Dev. Biol. 55, 119–130 (2016).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  175. Sugimura, K., Lenne, P.-F. & Graner, F. Measuring forces and stresses in situ in living tissues. Development 143, 186–196 (2016).

    Article  CAS  PubMed  Google Scholar 

  176. Barriga, E. H., Franze, K., Charras, G. & Mayor, R. Tissue stiffening coordinates morphogenesis by triggering collective cell migration in vivo. Nature 554, 523–527 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  177. Harris, A. R., Daeden, A. & Charras, G. T. Formation of adherens junctions leads to the emergence of a tissue-level tension in epithelial monolayers. J. Cell Sci. 127, 2507–2517 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  178. Wang, Y., Meng, F. & Sachs, F. Genetically encoded force sensors for measuring mechanical forces in proteins. Commun. Integr. Biol. 4, 385–390 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  179. Borghi, N. et al. E-cadherin is under constitutive actomyosin-generated tension that is increased at cell–cell contacts upon externally applied stretch. Proc. Natl Acad. Sci. USA 109, 12568–12573 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  180. Moussa, R. et al. An evaluation of genetically encoded FRET-based biosensors for quantitative metabolite analyses in vivo. J. Biotechnol. 191, 250–259 (2014).

    Article  CAS  PubMed  Google Scholar 

  181. Fu, J. et al. Mechanical regulation of cell function with geometrically modulated elastomeric substrates. Nat. Methods 7, 733–736 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  182. Ferro, V., Chuai, M., Mcgloin, D. & Weijer, C. J. Measurement of junctional tension in epithelial cells at the onset of primitive streak formation in the chick embryo via non-destructive optical manipulation. Development 147, dev175109 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  183. Hörner, F. et al. Holographic optical tweezers-based in vivo manipulations in zebrafish embryos. J. Biophotonics 10, 1492–1501 (2017).

    Article  PubMed  Google Scholar 

  184. Maître, J. L., Niwayama, R., Turlier, H., Nedelec, F. & Hiiragi, T. Pulsatile cell-autonomous contractility drives compaction in the mouse embryo. Nat. Cell Biol. 17, 849–855 (2015).

    Article  PubMed  CAS  Google Scholar 

  185. Tanase, M., Biais, N. & Sheetz, M. Magnetic tweezers in cell biology. Methods Cell Biol. 83, 473–493 (2007).

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors thank all members of the Brivanlou laboratory, C. LaBonne, O. Campàs and participants in the 2021 Marine Biological Laboratory (MBL) Embryology Advanced Research Training Course for useful discussions and comments. M.V. is supported by the Human Frontier Science Program (HFSP) fellowship LT000283-2020-C. E.D.S. is supported by National Science Foundation (NSF) grant No. 2013131.

Author information

Authors and Affiliations

Authors

Contributions

The authors contributed equally to all aspects of the article.

Corresponding author

Correspondence to Ali H. Brivanlou.

Ethics declarations

Competing interests

A.H.B. and E.D.S. are co-founders of RUMi Scientific. A.H.B. is the co-founder of OvaNova Laboratories. M.V. declares no competing interests.

Additional information

Peer review information

Nature Reviews Molecular Cell Biology thanks the anonymous reviewers for their contribution to the peer review of this work.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Glossary

Rheology

The structural properties of a material that predict its dynamical behaviour when subject to a defined stress.

Bottle cells

In the early Xenopus laevis gastrula, elongated epithelial cells undergoing apical constriction at the site of the blastopore formation.

Blastopore

A circular and transient morphological structure located on the dorsal side in amphibians, through which the mesoderm is internalized during early gastrulation.

Convergent extension

Tissue-scale deformation, whereby the tissue stretches in one direction and narrows in the orthogonal axis owing to the radial intercalation of cells into the elongating layer.

Blastomeres

Cells produced by the early cleavages of the zygotic egg.

Force fields

Continuous force descriptions that represent as a vector field the physical interactions in a given system. For instance, in a developing embryo, a coarse-grained representation in which each individual force to which a cell is submitted within a tissue is computed.

Trophectoderm

An extra-embryonic tissue forming the outer layer of the mammalian blastocyst that envelops the embryo proper and supplies nutrients.

Durotaxis

A mode of cellular migration in which cells follow stiffness gradients as a long-range cue.

Jamming–unjamming

A special type of phase transition where increasing (jamming) or decreasing (unjamming) the packing of particles in a granular material leads to a macroscopic viscosity change. This theoretical framework has been used to describe the packing of cells in a biological tissue.

Wetting

The spreading of a liquid phase on top of another phase owing to favoured heterotypic interactions between the constituents of the two phases.

Epithelial–mesenchymal transition

A cellular transition whereby polarized epithelial cells lose adhesion with respect to one another and become independent (mesenchymal) and mobile. There is a spectrum of epithelial–mesenchymal transitions: that is, not all epithelial–mesenchymal transitions lead to fully mesenchymal cells.

Morphogen

As defined historically by Turing, a molecule secreted by a group of cells and acting from a distance on another group of cells, eliciting different outcomes in a dose-dependent manner.

Mechanical instabilities

Instabilities that appear when small fluctuations around an unstable equilibrium position drive the system towards two very different outcomes. The wrinkling or buckling of epithelial sheets is an example of a mechanical instability.

Mechano-transduction

Processes that convert extrinsic mechanical signals (for example, environmental stiffness or a force from a neighbouring cell) into an intrinsic change in the intracellular biochemical, transcriptional or bioelectrical activity of the cell.

Planar cell polarity (PCP) pathway

The signalling pathway that regulates the polarization of a field of cells within the plane of a cell sheet. This process is involved in various developmental events, including convergent extension.

Hippo pathway

The signalling pathway associated with cell proliferation, tissue and organ growth, size determination and mechanosensation.

Nodal

A morphogen belonging to the super TGFβ family, initially named because of its association with the node structure in the developing mouse embryo.

Node

A small structure at the anterior part of the primitive streak.

Basal body

A protein structure found at the basis of eukaryotic cilia that serves as a nucleation site for microtubules.

Chiral molecules

Molecules that cannot be superposed to their mirrored image by any combination of rotations. Chiral molecules often have different reactivities.

Primitive streak

A transient embryonic tissue acting as a signalling centre and a point of conversion to mesendoderm. Morphologically, an elongated depression that progresses from the posterior to the anterior part of the epiblastic disc.

Involution

Specific morphogenetic event happening during gastrulation that involves the collective motion of cells that spread inwards by rolling around a boundary imposed by bottle cells, leading to basal to basal juxtaposition of the internal and external cells.

Convergent thickening

A process whereby cells rearrange themselves and leave the surface of the tissue to invade the space in-between, leading to shortening and thickening of the tissue.

Epiboly

The partial enveloping of one cell population by another in early developmental processes, owing to proliferation differences between the two tissues.

Neural crest

A transient cell population in vertebrates that originates from the ectoderm.

Surface tension

Modelized as a force per unit of length or as an energy per unit of area, tension that results from the cost of maintaining an interface between two fluid-like systems having a homotypic interaction (between molecules or cells of the same type) more favourable than the heterotypic interaction (between molecules or cells of a different type).

Ephrin signalling pathway

A cell–cell signalling mechanism involving, on one side, Eph receptor kinases (transmembrane proteins) and, on the other, their membrane-tethered ligands called ephrins. This signalling has been intensely investigated in the context of the nervous system development and is involved in cell sorting, positioning and migration.

Blastoderm

Usually, the initial population of embryonic superficial cells on top of the yolk (in a yolky embryo such as the chick or the zebrafish).

Competence

For an embryonic cell, being competent means being able to respond to inductive signals. As mechanics shape the potential of cells to be responsive in a specific time and space window, it is likely that competence is also affected by mechanical forces.

Gastruloids

In vitro assembled 2D or 3D aggregates of pluripotent embryonic cells that model some aspects of in vivo gastrulation, whereby cells self-organize to generate patterns of embryonic and extra-embryonic tissues.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Valet, M., Siggia, E.D. & Brivanlou, A.H. Mechanical regulation of early vertebrate embryogenesis. Nat Rev Mol Cell Biol 23, 169–184 (2022). https://doi.org/10.1038/s41580-021-00424-z

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41580-021-00424-z

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing