TY - JOUR
T1 - Topological defects in the nematic order of actin fibres as organization centres of Hydra morphogenesis
AU - Maroudas-Sacks, Yonit
AU - Garion, Liora
AU - Shani-Zerbib, Lital
AU - Livshits, Anton
AU - Braun, Erez
AU - Keren, Kinneret
N1 - Funding Information: We thank G. Ben Yoseph for technical assistance; N. Dahan from the LS&E Imaging and Microscopy Unit for help with confocal and light-sheet microscopy; B. Hobmayer for providing transgenic Hydra expressing lifeact-GFP; V. Vitelli, C. Marchetti and J. Yeomans for discussions; N. Dye and M. Driscoll for advice on image analysis; and P. Silberzan, A. Mogilner, J. Prost, N. Dye, Y. Kafri, T. Schultheiss, G. Bunin, A. Frishman and N. Ierushalmi for comments on the manuscript. This work was supported by a grant from the European Research Council (ERC-2018-COG grant number 819174) to K.K., a grant from the Israel Science Foundation (grant number 228/17) to E.B. and a Miriam and Aaron Gutwirth Memorial Fellowship to Y.M.-S. Publisher Copyright: © 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021/2
Y1 - 2021/2
N2 - Animal morphogenesis arises from the complex interplay between multiple mechanical and biochemical processes with mutual feedback. Developing an effective, coarse-grained description of morphogenesis is essential for understanding how these processes are coordinated across scales to form robust, functional outcomes. Here we show that the nematic order of the supracellular actin fibres in regenerating Hydra defines a slowly varying field, whose dynamics provide an effective description of the morphogenesis process. We show that topological defects in this field, which are long-lived yet display rich dynamics, act as organization centres with morphological features developing at defect sites. These observations suggest that the nematic orientation field can be considered a ‘mechanical morphogen’ whose dynamics, in conjugation with various biochemical and mechanical signalling processes, result in the robust emergence of functional patterns during morphogenesis.
AB - Animal morphogenesis arises from the complex interplay between multiple mechanical and biochemical processes with mutual feedback. Developing an effective, coarse-grained description of morphogenesis is essential for understanding how these processes are coordinated across scales to form robust, functional outcomes. Here we show that the nematic order of the supracellular actin fibres in regenerating Hydra defines a slowly varying field, whose dynamics provide an effective description of the morphogenesis process. We show that topological defects in this field, which are long-lived yet display rich dynamics, act as organization centres with morphological features developing at defect sites. These observations suggest that the nematic orientation field can be considered a ‘mechanical morphogen’ whose dynamics, in conjugation with various biochemical and mechanical signalling processes, result in the robust emergence of functional patterns during morphogenesis.
UR - https://www.scopus.com/pages/publications/85096446927
U2 - 10.1038/s41567-020-01083-1
DO - 10.1038/s41567-020-01083-1
M3 - Article
SN - 1745-2473
VL - 17
SP - 251
EP - 259
JO - Nature Physics
JF - Nature Physics
IS - 2
ER -