Mechanical feedback defines organizing centers to drive digit emergence.

chondrogenesis digit limb development mechanical feedback mechanobiology organizing centers phalanx-forming region/digit crescent self-organization tissue mechanics

Journal

Developmental cell
ISSN: 1878-1551
Titre abrégé: Dev Cell
Pays: United States
ID NLM: 101120028

Informations de publication

Date de publication:
11 04 2022
Historique:
received: 01 09 2021
revised: 25 01 2022
accepted: 10 03 2022
entrez: 12 4 2022
pubmed: 13 4 2022
medline: 15 4 2022
Statut: ppublish

Résumé

During embryonic development, digits gradually emerge in a periodic pattern. Although genetic evidence indicates that digit formation results from a self-organizing process, the underlying mechanisms are still unclear. Here, we find that convergent-extension tissue flows driven by active stresses underlie digit formation. These active stresses simultaneously shape cartilage condensations and lead to the emergence of a compressive stress region that promotes high activin/p-SMAD/SOX9 expression, thereby defining digit-organizing centers via a mechanical feedback. In Wnt5a mutants, such mechanical feedback is disrupted due to the loss of active stresses, organizing centers do not emerge, and digit formation is precluded. Thus, digit emergence does not result solely from molecular interactions, as was previously thought, but requires a mechanical feedback that ensures continuous coupling between phalanx specification and elongation. Our work, which links mechanical and molecular signals, provides a mechanistic context for the emergence of organizing centers that may underlie various developmental processes.

Identifiants

pubmed: 35413235
pii: S1534-5807(22)00164-2
doi: 10.1016/j.devcel.2022.03.004
pii:
doi:

Substances chimiques

Activins 104625-48-1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

854-866.e6

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Carolina Parada (C)

Department of Developmental and Stem Cell Biology, Institut Pasteur, 75724 Paris Cedex 15, France; CNRS UMR 3738, 25 rue du Dr Roux, 75015 Paris, France.

Samhita P Banavar (SP)

Department of Physics, University of California, Santa Barbara, CA 93106-5070, USA.

Parisa Khalilian (P)

Department of Developmental and Stem Cell Biology, Institut Pasteur, 75724 Paris Cedex 15, France; CNRS UMR 3738, 25 rue du Dr Roux, 75015 Paris, France.

Stephane Rigaud (S)

Image Analysis Hub, C2RT, Institut Pasteur, 75724 Paris Cedex 15, France.

Arthur Michaut (A)

Department of Developmental and Stem Cell Biology, Institut Pasteur, 75724 Paris Cedex 15, France; CNRS UMR 3738, 25 rue du Dr Roux, 75015 Paris, France.

Yucen Liu (Y)

Department of Mechanical Engineering, University of California, Santa Barbara, CA 93106-5070, USA.

Dennis Manjaly Joshy (DM)

Department of Mechanical Engineering, University of California, Santa Barbara, CA 93106-5070, USA.

Otger Campàs (O)

Department of Mechanical Engineering, University of California, Santa Barbara, CA 93106-5070, USA; Department of Molecular, Cell and Developmental Biology, University of California, Santa Barbara, CA, USA; Cluster of Excellence Physics of Life, TU Dresden, 01062 Dresden, Germany. Electronic address: otger.campas@tu-dresden.de.

Jerome Gros (J)

Department of Developmental and Stem Cell Biology, Institut Pasteur, 75724 Paris Cedex 15, France; CNRS UMR 3738, 25 rue du Dr Roux, 75015 Paris, France. Electronic address: jgros@pasteur.fr.

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Classifications MeSH