Evidence map›Paper›PMID 34032267›Full record

ArticleDevelopment (Cambridge, England)2021

MEIS-WNT5A axis regulates development of fourth ventricle choroid plexus.

Karol Kaiser, Ahram Jang, Petra Kompanikova, Melody P Lun, Jan Prochazka, Ondrej Machon, Neil Dani, Michaela Prochazkova, Benoit Laurent, Daniel Gyllborg and 11 more

Erratum issuedOpen access · greenAbstract 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. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  6. Review
  7. ChFluids and barriers of the CNS · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Regulation of choroid plexus development and its functions.Cellular and molecular life sciences : CMLS · 2022
    Review
  15. Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 10 institutions in 7 countries.

Karol KaiserDepartment of Experimental Biology, Faculty of Science, Masaryk University, Brno 61137, Czech Republic.ORCID 0000-0003-4705-2003
Ahram JangDepartment of Pathology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0002-4286-4718
Petra KompanikovaDepartment of Experimental Biology, Faculty of Science, Masaryk University, Brno 61137, Czech Republic.ORCID 0000-0002-3742-4523
Melody P LunDepartment of Pathology, Boston Children's Hospital, Boston, MA 02115, USA.
Jan ProchazkaCzech Centre for Phenogenomics and Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the CAS, Prague 142 20, Czech Republic.ORCID 0000-0003-4675-8995
Ondrej MachonLaboratory of Transcriptional Regulation, Institute of Molecular Genetics of the CAS, Prague 142 20, Czech Republic.ORCID 0000-0002-5139-1406
Neil DaniDepartment of Pathology, Boston Children's Hospital, Boston, MA 02115, USA.
Michaela ProchazkovaCzech Centre for Phenogenomics and Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the CAS, Prague 142 20, Czech Republic.ORCID 0000-0002-3773-8995
Benoit LaurentResearch Center on Aging, CIUSSS de l'Estrie - CHUS, Sherbrooke, QC 75361, Canada.
Daniel GyllborgScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Solna SE-106 91, Sweden.ORCID 0000-0002-1429-6426
Renee van AmerongenSwammerdam Institute for Life Sciences, Section of Molecular Cytology, Faculty of Science, University of Amsterdam1098 XH, Netherlands.ORCID 0000-0002-8808-2092
Ryann M FameDepartment of Pathology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0002-8244-2624
Suhasini GuptaDepartment of Pathology, Boston Children's Hospital, Boston, MA 02115, USA.
Feizhen WuShanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China.ORCID 0000-0002-1265-9887
Roger A BarkerJohn van Geest Centre for Brain Repair and WT-MRC Cambridge Stem Cell Centre, University of Cambridge, Cambridge CB2 0PY, UK.ORCID 0000-0001-8843-7730
Ivana BukovaCzech Centre for Phenogenomics and Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the CAS, Prague 142 20, Czech Republic.
Radislav SedlacekCzech Centre for Phenogenomics and Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the CAS, Prague 142 20, Czech Republic.ORCID 0000-0002-3352-392X
Zbynek KozmikLaboratory of Transcriptional Regulation, Institute of Molecular Genetics of the CAS, Prague 142 20, Czech Republic.ORCID 0000-0002-5850-2105
Ernest ArenasDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm 171 77, Sweden.ORCID 0000-0003-0197-6577
Maria K LehtinenDepartment of Pathology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0002-7243-2967
Vitezslav BryjaDepartment of Experimental Biology, Faculty of Science, Masaryk University, Brno 61137, Czech Republic.ORCID 0000-0002-9136-5085
Boston Children's Hospital · USCzech Academy of Sciences, Institute of Molecular Genetics · CZMasaryk University · CZCzech Academy of Sciences, Institute of Experimental Medicine · CZKarolinska Institutet · SENetherlands Institute for Neuroscience · NLStockholm University · SESun Yat-sen University · CNUniversité de Sherbrooke · CAWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Control of neural stem cells by the nascent cerebrospinal fluidR01NS088566 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI LEHTINEN, MARIA · 2014 to 2024
$5.5M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Department of HealthMedical Research Council MC_PC_17230NICHD NIH HHS U54 HD090255NINDS NIH HHS R01 NS088566Wellcome Trust
6 · The paper itself

Abstract

The choroid plexus (ChP) produces cerebrospinal fluid and forms an essential brain barrier. ChP tissues form in each brain ventricle, each one adopting a distinct shape, but remarkably little is known about the mechanisms underlying ChP development. Here, we show that epithelial WNT5A is crucial for determining fourth ventricle (4V) ChP morphogenesis and size in mouse. Systemic Wnt5a knockout, or forced Wnt5a overexpression beginning at embryonic day 10.5, profoundly reduced ChP size and development. However, Wnt5a expression was enriched in Foxj1-positive epithelial cells of 4V ChP plexus, and its conditional deletion in these cells affected the branched, villous morphology of the 4V ChP. We found that WNT5A was enriched in epithelial cells localized to the distal tips of 4V ChP villi, where WNT5A acted locally to activate non-canonical WNT signaling via ROR1 and ROR2 receptors. During 4V ChP development, MEIS1 bound to the proximal Wnt5a promoter, and gain- and loss-of-function approaches demonstrated that MEIS1 regulated Wnt5a expression. Collectively, our findings demonstrate a dual function of WNT5A in ChP development and identify MEIS transcription factors as upstream regulators of Wnt5a in the 4V ChP epithelium.

Indexed as

AnimalsBrainCell LineChoroid PlexusCRISPR-Cas SystemsEpithelial CellsEpitheliumFemaleFourth VentricleHEK293 CellsHumansMiceMice, KnockoutMyeloid Ecotropic Viral Integration Site 1 ProteinPromoter Regions, GeneticReceptor Tyrosine Kinase-like Orphan ReceptorsMeis1 protein, mouseMyeloid Ecotropic Viral Integration Site 1 ProteinReceptor Tyrosine Kinase-like Orphan ReceptorsRor1 protein, mouseRor2 protein, mouseWnt-5a ProteinWnt5a protein, mouseChoroid plexusEpitheliumMeis1Meis2MorphogenesisWNT5a

Identifiers

PMID34032267
PMCPMC8180257
OpenAlexW3159637870

What OpenQuestion holds

Textmetadata
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.