Evidence map›Paper›PMID 27825440›Full record

ArticleDevelopmental cell2016

EphrinB1/EphB3b Coordinate Bidirectional Epithelial-Mesenchymal Interactions Controlling Liver Morphogenesis and Laterality.

Jordi Cayuso, Aliaksandr Dzementsei, Johanna C Fischer, Gopal Karemore, Sara Caviglia, Josefin Bartholdson, Gavin J Wright, Elke A Ober

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

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  10. The zebrafish issue: 25 years on.Development (Cambridge, England) · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Jordi CayusoDivision of Developmental Biology, Mill Hill Laboratories, The Francis Crick Institute, London NW7 1AA, UK.
Aliaksandr DzementseiDanish Stem Cell Center (DanStem), University of Copenhagen, 2200 Copenhagen N, Denmark.
Johanna C FischerDivision of Developmental Biology, Mill Hill Laboratories, The Francis Crick Institute, London NW7 1AA, UK.
Gopal KaremoreNovo Nordisk Foundation Center for Protein Research, Protein Imaging Platform, University of Copenhagen, 2200 Copenhagen N, Denmark.
Sara CavigliaDanish Stem Cell Center (DanStem), University of Copenhagen, 2200 Copenhagen N, Denmark.
Josefin BartholdsonWellcome Trust Sanger Institute, Cell Surface Signalling Laboratory, Cambridge CB10 1HH, UK.
Gavin J WrightWellcome Trust Sanger Institute, Cell Surface Signalling Laboratory, Cambridge CB10 1HH, UK.
Elke A OberDivision of Developmental Biology, Mill Hill Laboratories, The Francis Crick Institute, London NW7 1AA, UK; Danish Stem Cell Center (DanStem), University of Copenhagen, 2200 Copenhagen N, Denmark. Electronic address: elke.ober@sund.ku.dk.
The Francis Crick Institute · GBUniversity of Copenhagen · DKWellcome Sanger Institute · GBNovo Nordisk Foundation · DK

Funding

Medical Research Council U117581329Wellcome Trust 098051
6 · The paper itself

Abstract

Positioning organs in the body often requires the movement of multiple tissues, yet the molecular and cellular mechanisms coordinating such movements are largely unknown. Here, we show that bidirectional signaling between EphrinB1 and EphB3b coordinates the movements of the hepatic endoderm and adjacent lateral plate mesoderm (LPM), resulting in asymmetric positioning of the zebrafish liver. EphrinB1 in hepatoblasts regulates directional migration and mediates interactions with the LPM, where EphB3b controls polarity and movement of the LPM. EphB3b in the LPM concomitantly repels hepatoblasts to move leftward into the liver bud. Cellular protrusions controlled by Eph/Ephrin signaling mediate hepatoblast motility and long-distance cell-cell contacts with the LPM beyond immediate tissue interfaces. Mechanistically, intracellular EphrinB1 domains mediate EphB3b-independent hepatoblast extension formation, while EpB3b interactions cause their destabilization. We propose that bidirectional short- and long-distance cell interactions between epithelial and mesenchyme-like tissues coordinate liver bud formation and laterality via cell repulsion.

Indexed as

Functional LateralityMorphogenesisAnimalsBody PatterningCell MovementCell ShapeEphrin-B1Ephrin-B3EpitheliumLiverMesodermPseudopodiaReceptors, Eph FamilyZebrafishZebrafish ProteinsEphB3b protein, zebrafishEphrin-B1Ephrin-B3Receptors, Eph FamilyZebrafish ProteinsbidirectionalEphB3EphrinB1lateral plate mesodermlivermigrationmorphogenesisprotrusionrepulsionzebrafish

Identifiers

PMID27825440
PMCPMC5107609
OpenAlexW2551651295

What OpenQuestion 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 OpenQuestion graph.