RhoA GEF Mcf2lb regulates rosette integrity during collective cell migration.

Apical constriction Cell migration Rosette morphogenesis Sensory development Zebrafish lateral line

Journal

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

Informations de publication

Date de publication:
01 Jan 2024
Historique:
received: 20 04 2023
accepted: 21 11 2023
medline: 2 1 2024
pubmed: 2 1 2024
entrez: 2 1 2024
Statut: ppublish

Résumé

Multicellular rosettes are transient epithelial structures that serve as important cellular intermediates in the formation of diverse organs. Using the zebrafish posterior lateral line primordium (pLLP) as a model system, we investigated the role of the RhoA GEF Mcf2lb in rosette morphogenesis. The pLLP is a group of ∼150 cells that migrates along the zebrafish trunk and is organized into epithelial rosettes; these are deposited along the trunk and will differentiate into sensory organs called neuromasts (NMs). Using single-cell RNA-sequencing and whole-mount in situ hybridization, we showed that mcf2lb is expressed in the pLLP during migration. Live imaging and subsequent 3D analysis of mcf2lb mutant pLLP cells showed disrupted apical constriction and subsequent rosette organization. This resulted in an excess number of deposited NMs along the trunk of the zebrafish. Cell polarity markers ZO-1 and Par-3 were apically localized, indicating that pLLP cells are properly polarized. In contrast, RhoA activity, as well as signaling components downstream of RhoA, Rock2a and non-muscle Myosin II, were diminished apically. Thus, Mcf2lb-dependent RhoA activation maintains the integrity of epithelial rosettes.

Identifiants

pubmed: 38165177
pii: 340220
doi: 10.1242/dev.201898
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : R01GM130868
Pays : United States

Informations de copyright

© 2024. Published by The Company of Biologists Ltd.

Déclaration de conflit d'intérêts

Competing interests The authors declare no competing or financial interests.

Auteurs

Hannah M Olson (HM)

Department of Cell, Developmental & Cancer Biology, Oregon Health & Science University, The Knight Cancer Institute, Portland, OR 97239, USA.
Neuroscience Graduate Program, Oregon Health & Science University, Portland, OR 97239, USA.

Amanda Maxfield (A)

Department of Cell, Developmental & Cancer Biology, Oregon Health & Science University, The Knight Cancer Institute, Portland, OR 97239, USA.

Nicholas L Calistri (NL)

Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.
Biomedical Engineering Graduate Program, Oregon Health & Science University, Portland, OR 97239, USA.

Laura M Heiser (LM)

Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.

Weiyi Qian (W)

Skirball Institute of Biomolecular Medicine, New York University Grossman School of Medicine, New York, NY 10016, USA.

Holger Knaut (H)

Skirball Institute of Biomolecular Medicine, New York University Grossman School of Medicine, New York, NY 10016, USA.

Alex V Nechiporuk (AV)

Department of Cell, Developmental & Cancer Biology, Oregon Health & Science University, The Knight Cancer Institute, Portland, OR 97239, USA.

Classifications MeSH