Evidence map›Paper›PMID 33932333›Full record

ArticleDevelopmental cell2021

Formation of polarized contractile interfaces by self-organized Toll-8/Cirl GPCR asymmetry.

Jules Lavalou, Qiyan Mao, Stefan Harmansa, Stephen Kerridge, Annemarie C Lellouch, Jean-Marc Philippe, Stephane Audebert, Luc Camoin, Thomas Lecuit

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 72 citations in OpenAlex.

  1. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
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  11. The Geometric Basis of Epithelial Convergent Extension.bioRxiv : the preprint server for biology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Jules LavalouAix-Marseille Université & CNRS, IBDM - UMR7288 & Turing Centre for Living Systems, Marseille, France; Collège de France, Paris, France.
Qiyan MaoAix-Marseille Université & CNRS, IBDM - UMR7288 & Turing Centre for Living Systems, Marseille, France. Electronic address: qiyan.mao@univ-amu.fr.
Stefan HarmansaAix-Marseille Université & CNRS, IBDM - UMR7288 & Turing Centre for Living Systems, Marseille, France.
Stephen KerridgeAix-Marseille Université & CNRS, IBDM - UMR7288 & Turing Centre for Living Systems, Marseille, France.
Annemarie C LellouchAix-Marseille Université & CNRS, IBDM - UMR7288 & Turing Centre for Living Systems, Marseille, France.
Jean-Marc PhilippeAix-Marseille Université & CNRS, IBDM - UMR7288 & Turing Centre for Living Systems, Marseille, France.
Stephane AudebertCentre de Recherche en Cancérologie de Marseille, Marseille Proteomics, Aix-Marseille Université, Inserm, CNRS, Institut Paoli Calmettes, Marseille, France.
Luc CamoinCentre de Recherche en Cancérologie de Marseille, Marseille Proteomics, Aix-Marseille Université, Inserm, CNRS, Institut Paoli Calmettes, Marseille, France.
Thomas LecuitAix-Marseille Université & CNRS, IBDM - UMR7288 & Turing Centre for Living Systems, Marseille, France; Collège de France, Paris, France. Electronic address: thomas.lecuit@univ-amu.fr.
Living Systems (United States) · USInstitut de Biologie du Développement Marseille · FRAix-Marseille Université · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interfaces between cells with distinct genetic identities elicit signals to organize local cell behaviors driving tissue morphogenesis. The Drosophila embryonic axis extension requires planar polarized enrichment of myosin-II powering oriented cell intercalations. Myosin-II levels are quantitatively controlled by GPCR signaling, whereas myosin-II polarity requires patterned expression of several Toll receptors. How Toll receptors polarize myosin-II and how this involves GPCRs remain unknown. Here, we report that differential expression of a single Toll receptor, Toll-8, polarizes myosin-II through binding to the adhesion GPCR Cirl/latrophilin. Asymmetric expression of Cirl is sufficient to enrich myosin-II, and Cirl localization is asymmetric at Toll-8 expression boundaries. Exploring the process dynamically, we reveal that Toll-8 and Cirl exhibit mutually dependent planar polarity in response to quantitative differences in Toll-8 expression between neighboring cells. Collectively, we propose that the cell surface protein complex Toll-8/Cirl self-organizes to generate local asymmetric interfaces essential for planar polarization of contractility.

Indexed as

AnimalsCell PolarityCytoskeletal ProteinsDrosophila melanogasterDrosophila ProteinsEmbryonic DevelopmentGene Expression Regulation, DevelopmentalMembrane ProteinsMorphogenesisMultiprotein ComplexesMuscle ContractionMyosin Type IIReceptors, G-Protein-CoupledReceptors, PeptideToll-Like Receptor 8CIRL protein, DrosophilaCytoskeletal ProteinsDrosophila ProteinsMembrane ProteinsMultiprotein ComplexesMyosin Type IIReceptors, G-Protein-CoupledReceptors, PeptideToll-Like Receptor 8GPCRlatrophilinmechanicsmorphogenesisPCPpolarityToll receptors

Identifiers

PMID33932333
PMCPMC8207821
OpenAlexW3159077374

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.