Evidence map›Paper›PMID 34028355›Full record

ArticleeLife2021

Wnt- and glutamate-receptors orchestrate stem cell dynamics and asymmetric cell division.

Sergi Junyent, Joshua C Reeves, James LA Szczerkowski, Clare L Garcin, Tung-Jui Trieu, Matthew Wilson, Jethro Lundie-Brown, Shukry J Habib

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in eLife, 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
0.9field-weighted citation impact, top 27% 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, 17 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Sergi Junyent *Centre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.ORCID 0000-0003-2405-5885
Joshua C Reeves *Centre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.ORCID 0000-0001-7373-576X
James LA SzczerkowskiCentre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.
Clare L GarcinCentre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.
Tung-Jui TrieuCentre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.
Matthew WilsonCentre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.
Jethro Lundie-BrownCentre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.ORCID 0000-0003-3403-1094
Shukry J HabibCentre for Stem Cells and Regenerative Medicine, King's College London, London, United Kingdom.ORCID 0000-0003-3132-2216
King's College London · GB

Funding

Department of HealthMedical Research Council MR/K017047/1Medical Research Council MR/R015635/1Wellcome TrustWellcome Trust 102513/Z/13/Z
6 · The paper itself

Abstract

The Wnt-pathway is part of a signalling network that regulates many aspects of cell biology. Recently, we discovered crosstalk between AMPA/Kainate-type ionotropic glutamate receptors (iGluRs) and the Wnt-pathway during the initial Wnt3a-interaction at the cytonemes of mouse embryonic stem cells (ESCs). Here, we demonstrate that this crosstalk persists throughout the Wnt3a-response in ESCs. Both AMPA and Kainate receptors regulate early Wnt3a-recruitment, dynamics on the cell membrane, and orientation of the spindle towards a Wnt3a-source at mitosis. AMPA receptors specifically are required for segregating cell fate components during Wnt3a-mediated asymmetric cell division (ACD). Using Wnt-pathway component knockout lines, we determine that Wnt co-receptor Lrp6 has particular functionality over Lrp5 in cytoneme formation, and in facilitating ACD. Both Lrp5 and 6, alongside pathway effector β-catenin act in concert to mediate the positioning of the dynamic interaction with, and spindle orientation to, a localised Wnt3a-source. Wnt-iGluR crosstalk may prove pervasive throughout embryonic and adult stem cell signalling.

Indexed as

Cell DivisionWnt Signaling PathwayAnimalsbeta CateninCell DifferentiationCell LineCell LineageKainic Acid ReceptorsLow Density Lipoprotein Receptor-Related Protein-5Low Density Lipoprotein Receptor-Related Protein-6MiceMicroscopy, ConfocalMicroscopy, FluorescenceMicroscopy, VideoMouse Embryonic Stem CellsReceptor Cross-Talkbeta CateninCTNNB1 protein, mouseKainic Acid ReceptorsLow Density Lipoprotein Receptor-Related Protein-5Low Density Lipoprotein Receptor-Related Protein-6Lrp5 protein, mouseLrp6 protein, mouseReceptors, AMPAWnt3A ProteinWnt3a protein, mouseasymmetric cell divisioncell biologycytonemesglutamate receptorsmouseregenerative medicinespindle orientationstem cellstem cellsWnt signalling

Identifiers

PMID34028355
PMCPMC8177892
OpenAlexW3165478295

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.