Evidence map›Paper›PMID 31980653›Full record

ArticleNature communications2020

An optochemical tool for light-induced dissociation of adherens junctions to control mechanical coupling between cells.

Dirk Ollech, Tim Pflästerer, Adam Shellard, Chiara Zambarda, Joachim Pius Spatz, Philippe Marcq, Roberto Mayor, Richard Wombacher, Elisabetta Ada Cavalcanti-Adam

Erratum issuedAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Review
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  15. Review
  16. The mechanical forces that shape our senses.Development (Cambridge, England) · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. The Art of Engineering Biomimetic Cellular Microenvironments.ACS biomaterials science & engineering · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Dirk OllechDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-9490-7070
Tim PflästererDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120, Heidelberg, Germany.
Adam ShellardDepartment of Cell and Developmental Biology, University College London, London, WC1E 6BT, UK.
Chiara ZambardaDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120, Heidelberg, Germany.ORCID http://orcid.org/0000-0003-3730-8896
Joachim Pius SpatzDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120, Heidelberg, Germany.ORCID http://orcid.org/0000-0003-3419-9807
Philippe MarcqPMMH, CNRS, ESPCI Paris, PSL University, Sorbonne Université, Université de Paris, F-75005, Paris, France.ORCID http://orcid.org/0000-0002-3232-9156
Roberto MayorDepartment of Cell and Developmental Biology, University College London, London, WC1E 6BT, UK.
Richard Wombacher *Department of Pharmaceutical Chemistry, Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, INF 364, D-69120, Heidelberg, Germany. wombacher@uni-heidelberg.de.
Elisabetta Ada Cavalcanti-Adam *Department of Cellular Biophysics, Max Planck Institute for Medical Research, Jahnstraße 29, D-69120, Heidelberg, Germany. eacavalcanti@mr.mpg.de.ORCID http://orcid.org/0000-0003-0243-1552

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cadherin-catenin complex at adherens junctions (AJs) is essential for the formation of cell-cell adhesion and epithelium integrity; however, studying the dynamic regulation of AJs at high spatio-temporal resolution remains challenging. Here we present an optochemical tool which allows reconstitution of AJs by chemical dimerization of the force bearing structures and their precise light-induced dissociation. For the dimerization, we reconstitute acto-myosin connection of a tailless E-cadherin by two ways: direct recruitment of α-catenin, and linking its cytosolic tail to the transmembrane domain. Our approach enables a specific ON-OFF switch for mechanical coupling between cells that can be controlled spatially on subcellular or tissue scale via photocleavage. The combination with cell migration analysis and traction force microscopy shows a wide-range of applicability and confirms the mechanical contribution of the reconstituted AJs. Remarkably, in vivo our tool is able to control structural and functional integrity of the epidermal layer in developing Xenopus embryos.

Indexed as

ActomyosinAdherens Junctionsalpha CateninAnimalsAntigens, CDBiomechanical PhenomenaCadherinsCell LineCell MovementEpithelial CellsHumansLightMicroscopy, Atomic ForceOptical PhenomenaPhotochemical ProcessesXenopus laevisActomyosinalpha CateninAntigens, CDCadherinsCDH1 protein, humanCTNNA1 protein, human

Identifiers

PMID31980653
PMCPMC6981158

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Registered trials

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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.