Self-organized tissue mechanics underlie embryonic regulation.
Journal
Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462
Informations de publication
Date de publication:
11 Sep 2024
11 Sep 2024
Historique:
received:
31
03
2022
accepted:
09
08
2024
medline:
12
9
2024
pubmed:
12
9
2024
entrez:
11
9
2024
Statut:
aheadofprint
Résumé
Early amniote development is highly self-organized, capable of adapting to interference through local and long-range cell-cell interactions. This process, called embryonic regulation
Identifiants
pubmed: 39261736
doi: 10.1038/s41586-024-07934-8
pii: 10.1038/s41586-024-07934-8
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© 2024. The Author(s).
Références
Driesch, H. The Science and Philosophy of the Organism the Gifford Lectures Delivered Before the University of Aberdeen in the Year 1907–1908 (Adam and Charles Black, 1908).
Lutz, H. Sur la Production Expérimentale de la Polyembryonie et de la Monstruosité Double Chez les Oiseau (Université de Strasbourg, 1949).
Spratt, N. T. & Haas, H. Integrative mechanisms in development of the early chick blastoderm. I. Regulative potentiality of separated parts. J. Exp. Zool. 145, 97–137 (1960).
doi: 10.1002/jez.1401450202
Gräper, L. Die primitiventwicklung des hühnchens nach stereokinematographischen untersuchungen, kontrolliert durch vitale farbmarkierung und verglichen mit der entwicklung anderer wirbeltiere. Dev. Genes Evol. 116, 382–429 (1929).
Wetzel, R. Untersuchungen am Hühnchen. Die entwicklung des keims während der ersten beiden bruttage. Wilhelm Roux Arch. Entwickl. Mech. Org. 119, 188–321 (1929).
doi: 10.1007/BF02111186
pubmed: 28353845
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).
doi: 10.1126/science.aaw1965
pubmed: 31974255
Turing, A. M. The chemical basis of morphogenesis. Philos. Trans. R. Soc. Lond. B 237, 37–72 (1952).
Bertocchini, F. & Stern, C. D. GATA2 provides an early anterior bias and uncovers a global positioning system for polarity in the amniote embryo. Dev. Camb. Engl. 139, 4232–4238 (2012).
Seleiro, E. A., Connolly, D. J. & Cooke, J. Early developmental expression and experimental axis determination by the chicken Vg1 gene. Curr. Biol. 6, 1476–1486 (1996).
doi: 10.1016/S0960-9822(96)00752-X
pubmed: 8939612
Shah, S. B. et al. Misexpression of chick Vg1 in the marginal zone induces primitive streak formation. Dev. Camb. Engl. 124, 5127–5138 (1997).
Bertocchini, F. & Stern, C. D. The hypoblast of the chick embryo positions the primitive streak by antagonizing nodal signaling. Dev. Cell 3, 735–744 (2002).
doi: 10.1016/S1534-5807(02)00318-0
pubmed: 12431379
Bertocchini, F., Skromne, I., Wolpert, L. & Stern, C. D. Determination of embryonic polarity in a regulative system: evidence for endogenous inhibitors acting sequentially during primitive streak formation in the chick embryo. Development 131, 3381–3390 (2004).
doi: 10.1242/dev.01178
pubmed: 15226255
Torlopp, A. et al. The transcription factor Pitx2 positions the embryonic axis and regulates twinning. eLife 3, e03743 (2014).
doi: 10.7554/eLife.03743
pubmed: 25496870
pmcid: 4371885
Müller, P. & Schier, A. F. Extracellular movement of signaling molecules. Dev. Cell 21, 145–158 (2011).
doi: 10.1016/j.devcel.2011.06.001
pubmed: 21763615
pmcid: 3220056
Oster, G. F., Murray, J. D. & Harris, A. K. Mechanical aspects of mesenchymal morphogenesis. J. Embryol. Exp. Morphol. 78, 83–125 (1983).
Murray, J. D., Oster, G. F. & Harris, A. K. A mechanical model for mesenchymal morphogenesis. J. Math. Biol. 17, 125–129 (1983).
doi: 10.1007/BF00276117
pubmed: 6875405
Odell, G., Oster, G., Burnside, B. & Alberch, P. A mechanical model for epithelial morphogenesis. J. Math. Biol. 9, 291–295 (1980).
doi: 10.1007/BF00276030
pubmed: 7190180
Belintsev, B. N., Beloussov, L. V. & Zaraisky, A. G. Model of pattern formation in epithelial morphogenesis. J. Theor. Biol. 129, 369–394 (1987).
doi: 10.1016/S0022-5193(87)80019-X
pubmed: 3455468
Chapman, S. C., Schubert, F. R., Schoenwolf, G. C. & Lumsden, A. Analysis of spatial and temporal gene expression patterns in blastula and gastrula stage chick embryos. Dev. Biol. 245, 187–199 (2002).
doi: 10.1006/dbio.2002.0641
pubmed: 11969265
Mikawa, T., Poh, A. M., Kelly, K. A., Ishii, Y. & Reese, D. E. Induction and patterning of the primitive streak, an organizing center of gastrulation in the amniote. Dev. Dyn. Off. Publ. Am. Assoc. Anat. 229, 422–432 (2004).
Voiculescu, O., Bertocchini, F., Wolpert, L., Keller, R. E. & Stern, C. D. The amniote primitive streak is defined by epithelial cell intercalation before gastrulation. Nature 449, 1049–1052 (2007).
doi: 10.1038/nature06211
pubmed: 17928866
Rozbicki, E. et al. Myosin-II-mediated cell shape changes and cell intercalation contribute to primitive streak formation. Nat. Cell Biol. 17, 397–408 (2015).
doi: 10.1038/ncb3138
pubmed: 25812521
pmcid: 4886837
Bailles, A. et al. Genetic induction and mechanochemical propagation of a morphogenetic wave. Nature 572, 467–473 (2019).
doi: 10.1038/s41586-019-1492-9
pubmed: 31413363
pmcid: 8985608
Noll, N., Mani, M., Heemskerk, I., Streichan, S. J. & Shraiman, B. I. Active tension network model suggests an exotic mechanical state realized in epithelial tissues. Nat. Phys. 13, 1221–1226 (2017).
doi: 10.1038/nphys4219
pubmed: 30687408
pmcid: 6344062
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).
doi: 10.1073/pnas.1713682115
pubmed: 29784822
pmcid: 6004442
Mitrossilis, D. et al. Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation. Nat. Commun. 8, 13883 (2017).
doi: 10.1038/ncomms13883
pubmed: 28112149
pmcid: 5264015
Brunet, T. et al. Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria. Nat. Commun. 4, 2821 (2013).
doi: 10.1038/ncomms3821
pubmed: 24281726
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).
doi: 10.1016/j.devcel.2020.10.015
pubmed: 33207224
pmcid: 7755684
Skromne, I. & Stern, C. D. Interactions between Wnt and Vg1 signalling pathways initiate primitive streak formation in the chick embryo. Development 128, 2915–2927 (2001).
doi: 10.1242/dev.128.15.2915
pubmed: 11532915
Shyer, A. E. et al. Emergent cellular self-organization and mechanosensation initiate follicle pattern in the avian skin. Science 357, 811–815 (2017).
doi: 10.1126/science.aai7868
pubmed: 28705989
pmcid: 5605277
Oster, G. F., Murray, J. D. & Harris, A. K. Mechanical aspects of mesenchymal morphogenesis. Development 78, 83–125 (1983).
doi: 10.1242/dev.78.1.83
Gross, P. et al. Guiding self-organized pattern formation in cell polarity establishment. Nat. Phys. 15, 293–300 (2019).
doi: 10.1038/s41567-018-0358-7
pubmed: 31327978
Alnæs, M. et al. The FEniCS Project version 1.5. Arch. Numer. Softw. 3, 9–23 (2015).
Logg, A., Mardal, K.-A. & Wells, G. Automated Solution of Differential Equations by the Finite Element Method: The FEniCS Book (Springer, 2012).
Caldarelli, P. et al. Data for ‘Self-organized tissue mechanics underlie embryonic regulation’. Figshare https://doi.org/10.6084/m9.figshare.26004184 (2024).