Evidence map›Paper›PMID 33999996›Full record

ArticleDevelopment (Cambridge, England)2021

A combination of Notch signaling, preferential adhesion and endocytosis induces a slow mode of cell intercalation in the Drosophila retina.

Laura Blackie, Melda Tozluoglu, Mateusz Trylinski, Rhian F Walther, François Schweisguth, Yanlan Mao, Franck Pichaud

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  7. Review
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  11. Hexagonal patterning of the Drosophila eye.Developmental biology · 2021
    Review
  12. Neuronal immunoglobulin superfamily cell adhesion molecules in epithelial morphogenesis: insights fromPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Laura BlackieMRC Laboratory for Molecular Cell Biology (LMCB), University College London, London WC1E 6BT, UK.
Melda TozluogluMRC Laboratory for Molecular Cell Biology (LMCB), University College London, London WC1E 6BT, UK.
Mateusz TrylinskiMRC Laboratory for Molecular Cell Biology (LMCB), University College London, London WC1E 6BT, UK.
Rhian F WaltherMRC Laboratory for Molecular Cell Biology (LMCB), University College London, London WC1E 6BT, UK.
François SchweisguthDepartment of Developmental and Stem Cell Biology, Pasteur Institute, F-75015 Paris, France.
Yanlan MaoMRC Laboratory for Molecular Cell Biology (LMCB), University College London, London WC1E 6BT, UK.
Franck PichaudMRC Laboratory for Molecular Cell Biology (LMCB), University College London, London WC1E 6BT, UK.ORCID 0000-0002-8393-716X
MRC Laboratory for Molecular Cell Biology · GBCentre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Biotechnology and Biological Sciences Research Council BB/R000697Medical Research Council MC_12266BMedical Research Council MC_UU_12018/3Medical Research Council MR/L009056/1Medical Research Council MR/T031646/1Medical Research Council MR/V001256/1NIH HHS P40 OD018537Wellcome TrustWellcome Trust 103095
6 · The paper itself

Abstract

Movement of epithelial cells in a tissue occurs through neighbor exchange and drives tissue shape changes. It requires intercellular junction remodeling, a process typically powered by the contractile actomyosin cytoskeleton. This has been investigated mainly in homogeneous epithelia, where intercalation takes minutes. However, in some tissues, intercalation involves different cell types and can take hours. Whether slow and fast intercalation share the same mechanisms remains to be examined. To address this issue, we used the fly eye, where the cone cells exchange neighbors over ∼10 h to shape the lens. We uncovered three pathways regulating this slow mode of cell intercalation. First, we found a limited requirement for MyosinII. In this case, mathematical modeling predicts an adhesion-dominant intercalation mechanism. Genetic experiments support this prediction, revealing a role for adhesion through the Nephrin proteins Roughest and Hibris. Second, we found that cone cell intercalation is regulated by the Notch pathway. Third, we show that endocytosis is required for membrane removal and Notch activation. Taken together, our work indicates that adhesion, endocytosis and Notch can direct slow cell intercalation during tissue morphogenesis.

Indexed as

ActomyosinAdherens JunctionsAnimalsBody PatterningCell AdhesionCell Adhesion Molecules, NeuronalCell CommunicationDrosophilaDrosophila ProteinsEndocytosisEpithelial CellsEye ProteinsFocal AdhesionsMembrane ProteinsMyosin Type IIReceptors, NotchActomyosinCell Adhesion Molecules, NeuronalDrosophila ProteinsEye Proteinshbs protein, DrosophilaMembrane ProteinsMyosin Type IIN protein, DrosophilaReceptors, Notchrst protein, DrosophilaAdherens junctionAdhesionCell intercalationEpitheliaNephrinsNotch

Identifiers

PMID33999996
PMCPMC8180261
OpenAlexW3157781360

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.