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arxiv: 1907.10319 · v1 · pith:4V2CWD7Jnew · submitted 2019-07-24 · 🧬 q-bio.CB · physics.bio-ph· q-bio.TO

Stay hydrated: Basolateral fluids shaping tissues

Pith reviewed 2026-05-24 16:41 UTC · model grok-4.3

classification 🧬 q-bio.CB physics.bio-phq-bio.TO
keywords basolateral fluidintercellular fluidtissue shapingembryonic developmenthydrationmorphogenesismouse embryozebrafish embryo
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The pith

Basolateral fluid compartments shape tissues by controlling hydration levels during embryonic development.

A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.

The paper establishes that the composition and physical properties of intercellular fluid have a considerable impact on development. It focuses on basolateral fluid compartments in early mouse and zebrafish embryos to show how hydration levels are spatio-temporally controlled. These controls influence embryonic development and tissue shaping. A sympathetic reader would care because this adds the fluid environment as a key factor in morphogenesis beyond cellular mechanisms.

Core claim

Basolateral fluid compartments constitute an invisible engine for morphogenesis whose composition and physical properties considerably impact development, with hydration levels being spatio-temporally controlled to influence embryonic development in mouse and zebrafish models.

What carries the argument

Basolateral fluid compartments, the fluid-filled spaces adjacent to the basolateral membrane of cells, whose hydration regulates tissue mechanics and shape.

If this is right

  • The hydration levels of tissues are spatio-temporally controlled during development.
  • Fluid properties complement cellular properties in powering animal morphogenesis.
  • Recent studies in mouse and zebrafish provide models for how basolateral fluids influence organ shaping and positioning.

Where Pith is reading between the lines

These are editorial extensions of the paper, not claims the author makes directly.

  • This suggests that experimental perturbations of fluid composition could be used to test effects on specific developmental stages.
  • It opens connections to how fluid mechanics integrate with cell signaling in tissue patterning.
  • Similar mechanisms may apply to later stages of development or other species beyond the reviewed models.

Load-bearing premise

That the selected recent studies on basolateral compartments in mouse and zebrafish embryos provide representative evidence for the general role of fluid hydration in tissue shaping across development.

What would settle it

An experiment showing no effect of altered basolateral fluid hydration on tissue shapes or development in mouse or zebrafish embryos would falsify the central claim.

Figures

Figures reproduced from arXiv: 1907.10319 by Jean-L\'eon Ma\^itre, Markus Schliffka.

Figure 1
Figure 1. Figure 1: Cellular control of fluid compartments. Fluid movement between compartments is controlled by barriers such as epithelia or endothelia. Transmembrane pumps, transporters and channels control the distribution of osmolytes in both compartments [27]. Water follows the osmotic gradient established across the cellular barrier by flowing through aquaporins, which are water￾specific transmembrane channels [28,29].… view at source ↗
Figure 2
Figure 2. Figure 2: Basolateral lumen formation in the mouse blastocyst [PITH_FULL_IMAGE:figures/full_fig_p003_2.png] view at source ↗
Figure 3
Figure 3. Figure 3: Intercellular fluid distribution during doming in zebrafish embryos. At the onset of zebrafish gastrulation, surface cells become epithelial, separating the intercellular from the extraembryonic fluid. As this surface epithelium increases surface tension, deep cells are forced to rearrange radially [75] and intercellular fluid follows. However, because cell-cell adhesion is stronger at the margin of the ti… view at source ↗
read the original abstract

During development, embryos perform a mesmerizing choreography, which is crucial for the correct shaping, positioning and function of all organs. The cellular properties powering animal morphogenesis have been the focus of much attention. On the other hand, much less consideration has been given to the invisible engine constituted by the intercellular fluid. Cells are immersed in fluid, of which the composition and physical properties have a considerable impact on development. In this review, we revisit recent studies from the perspective of the fluid, focusing on basolateral fluid compartments and taking the early mouse and zebrafish embryos as models. These examples illustrate how the hydration levels of tissues are spatio-temporally controlled and influence embryonic development.

Editorial analysis

A structured set of objections, weighed in public.

Desk editor's note, referee report, simulated authors' rebuttal, and a circularity audit. Tearing a paper down is the easy half of reading it; the pith above is the substance, this is the friction.

Referee Report

1 major / 0 minor

Summary. The manuscript is a review paper arguing that the composition and physical properties of intercellular fluid, particularly in basolateral compartments, exert considerable influence on tissue shaping and embryonic development. It revisits selected recent studies in early mouse and zebrafish embryos as illustrative models to show how spatio-temporal control of tissue hydration levels affects morphogenesis.

Significance. If the synthesis holds, the review draws attention to an underappreciated physical aspect of morphogenesis that complements cell-based mechanisms. By reframing existing studies through the lens of fluid properties, it could stimulate targeted experiments on hydration dynamics in development.

major comments (1)
  1. [Abstract] Abstract, final sentence: the claim that the mouse and zebrafish examples 'illustrate how the hydration levels of tissues are spatio-temporally controlled and influence embryonic development' treats these two systems as representative without a systematic survey, cross-species comparison, or discussion of potential counterexamples in other embryos; this step is load-bearing for the broader assertion of a general role.

Simulated Author's Rebuttal

1 responses · 0 unresolved

We thank the referee for the constructive feedback on the abstract. The comment correctly identifies that the final sentence could be read as implying broader generality than the focused scope of the review intends. We address this below and will revise accordingly.

read point-by-point responses
  1. Referee: [Abstract] Abstract, final sentence: the claim that the mouse and zebrafish examples 'illustrate how the hydration levels of tissues are spatio-temporally controlled and influence embryonic development' treats these two systems as representative without a systematic survey, cross-species comparison, or discussion of potential counterexamples in other embryos; this step is load-bearing for the broader assertion of a general role.

    Authors: We agree that the wording risks overgeneralization. The review is explicitly framed as using mouse and zebrafish early embryos as illustrative models (see Introduction and the two main sections), not as a comprehensive survey. No cross-species comparison or counterexample analysis was performed because the manuscript is a targeted synthesis of recent work on basolateral fluid control rather than a meta-analysis. To prevent misreading, we will revise the abstract's final sentence to: 'These examples from mouse and zebrafish illustrate how the hydration levels of tissues can be spatio-temporally controlled and influence embryonic development in these systems.' We will also add a short clarifying sentence in the Discussion noting that extension to other species remains an open question for future work. revision: yes

Circularity Check

0 steps flagged

No circularity: literature review without derivations or self-referential predictions

full rationale

The paper is explicitly a review that revisits external studies on basolateral fluid compartments in mouse and zebrafish embryos. It contains no equations, no fitted parameters, no 'predictions' of any kind, and no load-bearing self-citations that reduce the central interpretive claim to its own inputs. The representativeness of the chosen model systems is an assumption of scope rather than a mathematical reduction; the text offers no derivation chain that collapses by construction. This is the normal non-circular outcome for a synthesis paper.

Axiom & Free-Parameter Ledger

0 free parameters · 0 axioms · 0 invented entities

This is a review paper; no free parameters, axioms, or invented entities are introduced by the authors. The text relies entirely on synthesis of prior published studies in developmental biology.

pith-pipeline@v0.9.0 · 5641 in / 1043 out tokens · 24520 ms · 2026-05-24T16:41:26.636095+00:00 · methodology

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Reference graph

Works this paper leans on

85 extracted references · 85 canonical work pages

  1. [1]

    Semin Cell Dev Biol 2016, 55:139–147

    Navis A, Nelson CM: Pulling together : Tissue-generated forces that drive lumen morphogenesis. Semin Cell Dev Biol 2016, 55:139–147

  2. [2]

    Cell 2013, 153:948–962

    Heisenberg C-P, Bellaïche Y: Forces in Tissue Morphogenesis and Patterning. Cell 2013, 153:948–962

  3. [3]

    Nat New Biol 1973, 245:251–253

    Garcia-Bellido A, Ripoll P, Morata G: Developmental Compartmentalisation of the Wing Disk of Drosophila. Nat New Biol 1973, 245:251–253

  4. [4]

    Dev Growth Differ 2017, 59:306–316

    Honda H: The world of epithelial sheets. Dev Growth Differ 2017, 59:306–316

  5. [5]

    Curr Biol 2019, 29:229–241

    Olstad EW, Ringers C, Hansen JN, Wens A, Brandt C, Wachten D, Yaksi E, Jurisch-Yaksi N: Ciliary Beating Compartmentalizes Cerebrospinal Fluid Flow in the Brain and Regulates Ventricular Development. Curr Biol 2019, 29:229–241

  6. [6]

    Development 2017, 144:1798–1806

    Krens SFG, Veldhuis JH, Barone V, Čapek D, Maître J-L, Brodland GW, Heisenberg C-P: Interstitial fluid osmolarity modulates the action of differential tissue surface tension in progenitor cell segregation during gastrulation. Development 2017, 144:1798–1806

  7. [7]

    J Inherit Metab Dis 1993, 16:617–638

    Segal MB: Extracellular and cerebrospinal fluids. J Inherit Metab Dis 1993, 16:617–638

  8. [8]

    Nature 1980, 284:550–552

    Pedersen RA, Spindle AI: Role of the blastocoele microenvironment in early mouse embryo differentiation. Nature 1980, 284:550–552

  9. [9]

    Development 2015, 142:3721–3733

    Sun G, Teh C, Shen H, Korzh V, Wohland T: Modulating the expression level of secreted Wnt3 influences cerebellum development in zebrafish transgenics. Development 2015, 142:3721–3733

  10. [10]

    Science 2016, 353:176–178

    Faubel R, Westendorf C, Bodenschatz E, Eichele G: Cilia-based flow network in the brain ventricles. Science 2016, 353:176–178

  11. [11]

    Dev Cell 2019, 49:171–188

    Moreau HD, Blanch-Mercader C, Attia R, Maurin M, Alraies Z, Sanséau D, Malbec O, Delgado M-G, Bousso P, Joanny J-F, et al.: Macropinocytosis Overcomes Directional Bias in Dendritic Cells Due to Hydraulic Resistance and Facilitates Space Exploration. Dev Cell 2019, 49:171–188

  12. [12]

    Annu Rev Cell Dev Biol 2015, 31:575–591

    Blasky AJ, Mangan A, Prekeris R: Polarized Protein Transport and Lumen Formation During Epithelial Tissue Morphogenesis. Annu Rev Cell Dev Biol 2015, 31:575–591

  13. [13]

    Trends Cell Biol 2015, 25:476–485

    Overeem AW, Bryant DM, van IJzendoorn SCD: Mechanisms of apical-basal axis orientation and epithelial lumen positioning. Trends Cell Biol 2015, 25:476–485

  14. [14]

    Nat Rev Mol Cell Biol 2016, 17:564–580

    Zihni C, Mills C, Matter K, Balda MS: Tight junctions: from simple barriers to multifunctional molecular gates. Nat Rev Mol Cell Biol 2016, 17:564–580

  15. [16]

    Science 2012, 336:721–724

    Müller P, Rogers KW, Jordan BM, Lee JS, Robson D, Ramanathan S, Schier AF: Differential Diffusivity of Nodal and Lefty Underlies a Reaction-Diffusion Patterning System. Science 2012, 336:721–724

  16. [17]

    Nature 2014, 515:120–124

    Durdu S, Iskar M, Revenu C, Schieber N, Kunze A, Bork P, Schwab Y, Gilmour D: Luminal signalling links cell communication to tissue architecture during organogenesis. Nature 2014, 515:120–124

  17. [18]

    Dev Cell 2016, 39:302–315

    Etoc F, Metzger J, Ruzo A, Kirst C, Yoney A, Ozair MZ, Brivanlou AH, Siggia ED: A Balance between Secreted Inhibitors and Edge Sensing Controls Gastruloid Self-Organization. Dev Cell 2016, 39:302–315

  18. [19]

    Nature 2003, 421:172–177

    Hove JR, Köster RW, Forouhar AS, Acevedo-Bolton G, Fraser SE, Gharib M: Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis. Nature 2003, 421:172–177

  19. [20]

    Dev Cell 2017, 43:274–289

    Duchemin A-L, Chen M, Vermot J, Li L, Morrisey EE, Morley MP, Scherrer-Crosbie M, Frank DB, Jameson SC, Bamezai S, et al.: Hemodynamic Forces Sculpt Developing Heart Valves through a KLF2-WNT9B Paracrine Signaling Axis. Dev Cell 2017, 43:274–289

  20. [21]

    Trends Cell Biol 2007, 17:44–50

    Rutkowski JM, Swartz MA: A driving force for change: interstitial flow as a morphoregulator. Trends Cell Biol 2007, 17:44–50

  21. [22]

    Proc Natl Acad Sci 2014, 111:2447–2452

    Polacheck WJ, German AE, Kamm RD, Ingber DE, Mammoto A: Mechanotransduction of fluid stresses governs 3D cell migration. Proc Natl Acad Sci 2014, 111:2447–2452

  22. [23]

    Elife 2017,

    Ferreira RR, Vilfan A, Jülicher F, Supatto W, Vermot J: Physical limits of flow sensing in the left-right organizer. Elife 2017,

  23. [24]

    Control of Corneal Size

    Coulombre AJ: The Role of Intraocular Pressure in the Development of the Chick Eye: II. Control of Corneal Size. AMA Arch Ophthalmol 1957, 57:250–253

  24. [25]

    Development 2010, 137:795–804

    Gutzman JH, Sive H: Epithelial relaxation mediated by the myosin phosphatase regulator Mypt1 is required for brain ventricle lumen expansion and hindbrain morphogenesis. Development 2010, 137:795–804

  25. [26]

    Nature 2019, 571:112–116

    Chan CJ, Costanzo M, Ruiz-Herrero T, Mönke G, Petrie RJ, Bergert M, Diz-Muñoz A, Mahadevan L, Hiiragi T: Hydraulic control of mammalian embryo size and cell fate. Nature 2019, 571:112–116

  26. [27]

    Adv Physiol Educ 2004, 28:143–154

    Dubyak GR: Ion homeostasis, channels, and transporters: an update on cellular mechanisms. Adv Physiol Educ 2004, 28:143–154

  27. [28]

    Am J Physiol Physiol 2000, 278:F13–F28

    Verkman AS, Mitra AK: Structure and function of aquaporin water channels. Am J Physiol Physiol 2000, 278:F13–F28

  28. [29]

    Biol Bull 2015, 229:6–23

    Finn RN, Cerdà J: Evolution and Functional Diversity of Aquaporins. Biol Bull 2015, 229:6–23

  29. [30]

    Nat Rev Mol Cell Biol 2014, 15:665–676

    Sigurbjörnsdóttir S, Mathew R, Leptin M: Molecular mechanisms of de novo lumen formation. Nat Rev Mol Cell Biol 2014, 15:665–676

  30. [31]

    Curr Biol 2011, 21:R126–R136

    Datta A, Bryant DM, Mostov KE: Molecular Regulation of Lumen Morphogenesis. Curr Biol 2011, 21:R126–R136

  31. [32]

    HFSP J 2009, 3:77–93

    Cartwright JHE, Piro O, Tuval I: Fluid dynamics in developmental biology: Moving fluids that shape ontogeny. HFSP J 2009, 3:77–93

  32. [33]

    Development 2012, 139:1229–1245

    Freund JB, Goetz JG, Hill KL, Vermot J: Fluid flows and forces in development: functions, features and biophysical principles. Development 2012, 139:1229–1245

  33. [34]

    Nat Rev Mol Cell Biol 2014, 15:225–242

    Rodriguez-Boulan E, Macara IG: Organization and execution of the epithelial polarity programme. Nat Rev Mol Cell Biol 2014, 15:225–242

  34. [35]

    Dev Dyn 1995, 202:405–420

    Müller H-AJ, Hausen P: Epithelial cell polarity in early Xenopus development. Dev Dyn 1995, 202:405–420

  35. [36]

    Dev Biol 2013, 382:70–81

    Danilchik M, Williams M, Brown E: Blastocoel-spanning filopodia in cleavage-stage Xenopus laevis: Potential roles in morphogen distribution and detection. Dev Biol 2013, 382:70–81

  36. [37]

    J Morphol 1985, 185:387–402

    Galileo DS, Morrill JB: Patterns of cells and extracellular material of the sea urchin Lytechinus variegatus (Echinodermata; Echinoidea) embryo, from hatched blastula to late gastrula. J Morphol 1985, 185:387–402

  37. [38]

    Nature 2017, 552:239–243

    Shahbazi MN, Scialdone A, Skorupska N, Weberling A, Recher G, Zhu M, Jedrusik A, Devito LG, Noli L, Macaulay IC, et al.: Pluripotent state transitions coordinate morphogenesis in mouse and human embryos. Nature 2017, 552:239–243

  38. [39]

    Nat Cell Biol 2010, 12:1035–1045

    Peränen J, Rodríguez-Fraticelli AE, Martín-Belmonte F, Datta A, Mostov KE, Bryant DM: A molecular network for de novo generation of the apical surface and lumen. Nat Cell Biol 2010, 12:1035–1045

  39. [40]

    Wang AZ, Ojakian GK, Nelson WJ: Steps in the morphogenesis of a polarized epithelium. I. Uncoupling the roles of cell-cell and cell-substratum contact in establishing plasma membrane polarity in multicellular epithelial (MDCK) cysts. J Cell Sci 1990, 95:137–151

  40. [41]

    Wang AZ, Ojakian GK, Nelson WJ: Steps in the morphogenesis of a polarized epithelium. II. Disassembly and assembly of plasma membrane domains during reversal of epithelial cell polarity in multicellular epithelial (MDCK) cysts. J Cell Sci 1990, 95:153–165

  41. [42]

    Nature 2018, 563:203–208

    Latorre E, Kale S, Casares L, Gómez-González M, Uroz M, Valon L, Nair R V., Garreta E, Montserrat N, del Campo A, et al.: Active superelasticity in three-dimensional epithelia of controlled shape. Nature 2018, 563:203–208

  42. [43]

    Nat Cell Biol 2018, 20:296–306

    Zajac O, Raingeaud J, Libanje F, Lefebvre C, Sabino D, Martins I, Roy P, Benatar C, Canet-Jourdan C, Azorin P, et al.: Tumour spheres with inverted polarity drive the formation of peritoneal metastases in patients with hypermethylated colorectal carcinomas. Nat Cell Biol 2018, 20:296–306

  43. [44]

    Biol Cell 2017, 109:323–338

    Maître JL: Mechanics of blastocyst morphogenesis. Biol Cell 2017, 109:323–338

  44. [45]

    Curr Top Dev Biol 2016, 117:275–288

    Rossant J: Making the Mouse Blastocyst: Past, Present, and Future. Curr Top Dev Biol 2016, 117:275–288

  45. [46]

    Wiley Interdiscip Rev Dev Biol 2016, 5:210–232

    Frankenberg SR, de Barros FRO, Rossant J, Renfree MB: The mammalian blastocyst. Wiley Interdiscip Rev Dev Biol 2016, 5:210–232

  46. [47]

    Nat Cell Biol 2015, 17:849–855

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

  47. [48]

    Dev Cell 2017, 40:235–247

    Korotkevich E, Niwayama R, Courtois A, Friese S, Berger N, Buchholz F, Hiiragi T: The Apical Domain Is Required and Sufficient for the First Lineage Segregation in the Mouse Embryo. Dev Cell 2017, 40:235–247

  48. [49]

    Cell 2018, 173:776–791

    Zenker J, White MD, Gasnier M, Alvarez YD, Lim HYG, Bissiere S, Biro M, Plachta N: Expanding Actin Rings Zipper the Mouse Embryo for Blastocyst Formation. Cell 2018, 173:776–791

  49. [50]

    In The Freezing of Mammalian Embryos

    Biggers JD, Borland RM, Powers RD: Transport mechanisms in the preimplantation mammalian embryo. In The Freezing of Mammalian Embryos. Excerpta Medica, Elsevier/North-Holland Amsterdam; 1977 52:129–146

  50. [51]

    Dev Biol 1989, 133:210–220

    Manejwala FM, Cragoe EJ, Schultz RM: Blastocoel expansion in the preimplantation mouse embryo: Role of extracellular sodium and chloride and possible apical routes of their entry. Dev Biol 1989, 133:210–220

  51. [52]

    Dev Biol 1977, 55:1–8

    Borland RM, Biggers JD, Lechene CP: Studies on the composition and formation of mouse blastocoele fluid using electron probe microanalysis. Dev Biol 1977, 55:1–8

  52. [53]

    Development 2017, 144:4422–4427

    Ruiz-Herrero T, Alessandri K, Gurchenkov B, Nassoy P, Mahadevan L: Organ size control via hydraulically gated oscillations. Development 2017, 144:4422–4427

  53. [54]

    Nat Mater 2015, 14:343–351

    Casares L, Vincent R, Zalvidea D, Campillo N, Navajas D, Arroyo M, Trepat X: Hydraulic fracture during epithelial stretching. Nat Mater 2015, 14:343–351

  54. [55]

    Proc Natl Acad Sci 2018, 115:10375–10380

    Leonavicius K, Royer C, Preece C, Davies B, Biggins JS, Srinivas S: Mechanics of mouse blastocyst hatching revealed by a hydrogel-based microdeformation assay. Proc Natl Acad Sci 2018, 115:10375–10380

  55. [56]

    Biochem Biophys Res Commun 2015, 456:562–566

    Park TJ, Kim SK, Wallingford JB: The planar cell polarity effector protein Wdpcp (Fritz) controls epithelial cell cortex dynamics via septins and actomyosin. Biochem Biophys Res Commun 2015, 456:562–566

  56. [57]

    Nature 2016, 536:344–348

    Maître J-L, Turlier H, Illukkumbura R, Eismann B, Niwayama R, Nédélec F, Hiiragi T: Asymmetric division of contractile domains couples cell positioning and fate specification. Nature 2016, 536:344–348

  57. [58]

    Proc Natl Acad Sci 2017, 114:5136–5141

    Alim K, Andrew N, Pringle A, Brenner MP: Mechanism of signal propagation in Physarum polycephalum. Proc Natl Acad Sci 2017, 114:5136–5141

  58. [59]

    Science 2006, 312:751–753

    Forouhar AS, Liebling M, Hickerson A, Nasiraei-Moghaddam A, Tsai H-J, Hove JR, Fraser SE, Dickinson ME, Gharib M: The Embryonic Vertebrate Heart Tube Is a Dynamic Suction Pump. Science 2006, 312:751–753

  59. [60]

    Science 2014, 344:409–412

    Wietek J, Wiegert JS, Adeishvili N, Schneider F, Watanabe H, Tsunoda SP, Vogt A, Elstner M, Oertner TG, Hegemann P: Conversion of Channelrhodopsin into a Light-Gated Chloride Channel. Science 2014, 344:409–412

  60. [61]

    Dev Biol 2007, 312:509–522

    Moriwaki K, Tsukita S, Furuse M: Tight junctions containing claudin 4 and 6 are essential for blastocyst formation in preimplantation mouse embryos. Dev Biol 2007, 312:509–522

  61. [62]

    Mol Cells 2004, 17:248–254

    Kim J, Gye MC, Kim MK: Role of occludin, a tight junction protein, in blastocoel formation, and in the paracellular permeability and differentiation of trophectoderm in preimplantation mouse embryos. Mol Cells 2004, 17:248–254

  62. [63]

    Mol Cell Biol 2008, 28:1669–1678

    Xu J, Kausalya PJ, Phua DCY, Ali SM, Hossain Z, Hunziker W: Early Embryonic Lethality of Mice Lacking ZO-2, but Not ZO-3, Reveals Critical and Nonredundant Roles for Individual Zonula Occludens Proteins in Mammalian Development. Mol Cell Biol 2008, 28:1669–1678

  63. [64]

    J Embryol Exp Morphol 1967, 17:481–490

    Cole RJ: Cinemicrographic observations on the trophoblast and zona pellucida of the mouse blastocyst. J Embryol Exp Morphol 1967, 17:481–490

  64. [65]

    Nature 2017, 545:103–107

    Pinheiro D, Hannezo E, Herszterg S, Bosveld F, Gaugue I, Balakireva M, Wang Z, Cristo I, Rigaud SU, Markova O, et al.: Transmission of cytokinesis forces via E-cadherin dilution and actomyosin flows. Nature 2017, 545:103–107

  65. [66]

    Dev Cell 2019, 48:445–459

    Stephenson RE, Higashi T, Erofeev IS, Arnold TR, Leda M, Goryachev AB, Miller AL: Rho Flares Repair Local Tight Junction Leaks. Dev Cell 2019, 48:445–459

  66. [67]

    Biophys J 2008, 95:978–985

    Kücken M, Soriano J, Pullarkat PA, Ott A, Nicola EM: An Osmoregulatory Basis for Shape Oscillations in Regenerating Hydra. Biophys J 2008, 95:978–985

  67. [68]

    Europhys Lett 2003, 64:137–143

    Fütterer C, Colombo C, Jülicher F, Ott A: Morphogenetic oscillations during symmetry breaking of regenerating Hydra vulgaris cells. Europhys Lett 2003, 64:137–143

  68. [69]

    J Anat 1966, 100:335–348

    Dickson AD: The form of the mouse blastocyst. J Anat 1966, 100:335–348

  69. [70]

    Development 1954, 2:1–13

    Lutwak-Mann C: Some properties of the rabbit blastocyst. Development 1954, 2:1–13

  70. [71]

    Curr Opin Cell Biol 2017, 48:33–39

    Williams ML, Solnica-Krezel L: Regulation of gastrulation movements by emergent cell and tissue interactions. Curr Opin Cell Biol 2017, 48:33–39

  71. [72]

    Int Rev Cytol 2007, 261:159–192

    Rohde LA, Heisenberg C: Zebrafish Gastrulation: Cell Movements, Signals, and Mechanisms. Int Rev Cytol 2007, 261:159–192

  72. [73]

    Dev Cell 2017, 40:354–366

    Morita H, Grigolon S, Bock M, Krens SFG, Salbreux G, Heisenberg C-P: The Physical Basis of Coordinated Tissue Spreading in Zebrafish Gastrulation. Dev Cell 2017, 40:354–366

  73. [74]

    Dev Biol 2010, 346:272–283

    Fukazawa C, Santiago C, Park KM, Deery WJ, Gomez de la Torre Canny S, Holterhoff CK, Wagner DS: poky/chuk/ikk1 is required for differentiation of the zebrafish embryonic epidermis. Dev Biol 2010, 346:272–283

  74. [75]

    Nat Commun 2017, 8:15431

    Reig G, Cerda M, Sepúlveda N, Flores D, Castañeda V, Tada M, Härtel S, Concha ML: Extra-embryonic tissue spreading directs early embryo morphogenesis in killifish. Nat Commun 2017, 8:15431

  75. [76]

    Biophys J 2018, 114:213–222

    Wallmeyer B, Trinschek S, Yigit S, Thiele U, Betz T: Collective Cell Migration in Embryogenesis Follows the Laws of Wetting. Biophys J 2018, 114:213–222

  76. [77]

    Nat Cell Biol 2019, 21:169–178

    Petridou NI, Grigolon S, Salbreux G, Hannezo E, Heisenberg C-P: Fluidization-mediated tissue spreading by mitotic cell rounding and non-canonical Wnt signalling. Nat Cell Biol 2019, 21:169–178

  77. [78]

    2008, 10:429–436

    Krieg M, Puech P, Käfer J, Graner F, Müller DJ, Heisenberg C: Tensile forces govern germ-layer organization in zebrafish. 2008, 10:429–436

  78. [79]

    Science 2012, 338:253–257

    Maître J-L, Berthoumieux H, Frederik S, Krens G, Salbreux G, Jülicher F, Paluch E, Heisenberg C: Adhesion Functions in Cell Sorting by Mechanically Coupling the Cortices of Adhering Cells. Science 2012, 338:253–257

  79. [80]

    Nature 2011, 469:226–230

    Stewart MP, Helenius J, Toyoda Y, Ramanathan SP, Muller DJ, Hyman AA: Hydrostatic pressure and the actomyosin cortex drive mitotic cell rounding. Nature 2011, 469:226–230

  80. [81]

    J Cell Sci 2009, 122:3233–3241

    Charras GT, Mitchison TJ, Mahadevan L: Animal cell hydraulics. J Cell Sci 2009, 122:3233–3241

Showing first 80 references.