Apical Relaxation during Mitotic Rounding Promotes Tension-Oriented Cell Division.


Journal

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

Informations de publication

Date de publication:
21 12 2020
Historique:
received: 21 04 2020
revised: 09 09 2020
accepted: 23 10 2020
pubmed: 19 11 2020
medline: 16 3 2021
entrez: 18 11 2020
Statut: ppublish

Résumé

Global tissue tension anisotropy has been shown to trigger stereotypical cell division orientation by elongating mitotic cells along the main tension axis. Yet, how tissue tension elongates mitotic cells despite those cells undergoing mitotic rounding (MR) by globally upregulating cortical actomyosin tension remains unclear. We addressed this question by taking advantage of ascidian embryos, consisting of a small number of interphasic and mitotic blastomeres and displaying an invariant division pattern. We found that blastomeres undergo MR by locally relaxing cortical tension at their apex, thereby allowing extrinsic pulling forces from neighboring interphasic blastomeres to polarize their shape and thus division orientation. Consistently, interfering with extrinsic forces by reducing the contractility of interphasic blastomeres or disrupting the establishment of asynchronous mitotic domains leads to aberrant mitotic cell division orientations. Thus, apical relaxation during MR constitutes a key mechanism by which tissue tension anisotropy controls stereotypical cell division orientation.

Identifiants

pubmed: 33207225
pii: S1534-5807(20)30836-4
doi: 10.1016/j.devcel.2020.10.016
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

695-706.e4

Subventions

Organisme : Austrian Science Fund FWF
ID : I 3601
Pays : Austria
Organisme : NICHD NIH HHS
ID : R01 HD088831
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests The authors declare no competing interests.

Auteurs

Benoit G Godard (BG)

Laboratoire de Biologie du Développement de Villefranche-sur-mer, Institut de la Mer de Villefranche-sur-mer, Sorbonne Université, CNRS, 06230 Villefranche-sur-mer, France; Institute of Science and Technology Austria, Klosterneuburg, Austria.

Rémi Dumollard (R)

Laboratoire de Biologie du Développement de Villefranche-sur-mer, Institut de la Mer de Villefranche-sur-mer, Sorbonne Université, CNRS, 06230 Villefranche-sur-mer, France.

Edwin Munro (E)

Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, IL 60637, USA.

Janet Chenevert (J)

Laboratoire de Biologie du Développement de Villefranche-sur-mer, Institut de la Mer de Villefranche-sur-mer, Sorbonne Université, CNRS, 06230 Villefranche-sur-mer, France.

Céline Hebras (C)

Laboratoire de Biologie du Développement de Villefranche-sur-mer, Institut de la Mer de Villefranche-sur-mer, Sorbonne Université, CNRS, 06230 Villefranche-sur-mer, France.

Alex McDougall (A)

Laboratoire de Biologie du Développement de Villefranche-sur-mer, Institut de la Mer de Villefranche-sur-mer, Sorbonne Université, CNRS, 06230 Villefranche-sur-mer, France.

Carl-Philipp Heisenberg (CP)

Institute of Science and Technology Austria, Klosterneuburg, Austria. Electronic address: heisenberg@ist.ac.at.

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Classifications MeSH