Primordial germ cells adjust their protrusion type while migrating in different tissue contexts in vivo.

Amoeboid motility Bleb Germ cell Migration Protrusion Zebrafish

Journal

Development (Cambridge, England)
ISSN: 1477-9129
Titre abrégé: Development
Pays: England
ID NLM: 8701744

Informations de publication

Date de publication:
15 01 2023
Historique:
received: 31 01 2022
accepted: 29 11 2022
pubmed: 15 12 2022
medline: 18 1 2023
entrez: 14 12 2022
Statut: ppublish

Résumé

In both physiological processes and disease contexts, migrating cells have the ability to adapt to conditions in their environment. As an in vivo model for this process, we use zebrafish primordial germ cells that migrate throughout the developing embryo. When migrating within an ectodermal environment, the germ cells form fewer and smaller blebs when compared with their behavior within mesodermal environment. We find that cortical tension of neighboring cells is a parameter that affects blebbing frequency. Interestingly, the change in blebbing activity is accompanied by the formation of more actin-rich protrusions. These alterations in cell behavior that correlate with changes in RhoA activity could allow the cells to maintain dynamic motility parameters, such as migration speed and track straightness, in different settings. In addition, we find that the polarity of the cells can be affected by stiff structures positioned in their migration path This article has an associated 'The people behind the papers' interview.

Identifiants

pubmed: 36515556
pii: 286614
doi: 10.1242/dev.200603
pmc: PMC10110502
pii:
doi:

Substances chimiques

Actins 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. Published by The Company of Biologists Ltd.

Déclaration de conflit d'intérêts

Competing interests The authors declare no competing or financial interests.

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Auteurs

Lukasz Truszkowski (L)

Institute of Cell Biology, ZMBE, University of Münster, D-48149 Münster, Germany.

Dilek Batur (D)

Institute of Cell Biology, ZMBE, University of Münster, D-48149 Münster, Germany.

Hongyan Long (H)

Bioactive Materials Laboratory, Max Planck Institute for Molecular Biomedicine, D-48149 Münster, Germany.

Katsiaryna Tarbashevich (K)

Institute of Cell Biology, ZMBE, University of Münster, D-48149 Münster, Germany.

Bart E Vos (BE)

Third Institute of Physics - Biophysics, Georg August University Göttingen, D-37007 Göttingen, Germany.

Britta Trappmann (B)

Bioactive Materials Laboratory, Max Planck Institute for Molecular Biomedicine, D-48149 Münster, Germany.

Erez Raz (E)

Institute of Cell Biology, ZMBE, University of Münster, D-48149 Münster, Germany.
Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.

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