Evidence map›Paper›PMID 19363157›Full record

ArticleDevelopment (Cambridge, England)2009

Non-canonical Wnt signaling regulates cell polarity in female reproductive tract development via van gogh-like 2.

Alysia L Vandenberg, David A Sassoon

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.4field-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

46 citing papers in PubMed, 87 citations in OpenAlex.

  1. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
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  8. Review
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  12. The pathological role of Wnt5a in psoriasis and psoriatic arthritis.Journal of cellular and molecular medicine · 2019
    Review
  13. Review
  14. Article
  15. Review
  16. Identification and characterization of a novel chemically induced allele at the planar cell polarity gene Vangl2.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Article
  17. Planar cell polarity signaling in the uterus directs appropriate positioning of the crypt for embryo implantation.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  18. Article
  19. Review
  20. 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

2 authors at 1 institution in 1 country.

Alysia L VandenbergUniversité Pierre et Marie Curie Paris VI, 75634 Paris Cedex 13, France.
David A Sassoon
Inserm · FR

Funding

Molecular basis of uterine cellular interactionsR01CA112686 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SASSOON, DAVID A · 2004 to 2008
$1.5M
NCI NIH HHS R019 R01CA112686
6 · The paper itself

Abstract

Wnt signaling effectors direct the development and adult remodeling of the female reproductive tract (FRT); however, the role of non-canonical Wnt signaling has not been explored in this tissue. The non-canonical Wnt signaling protein van gogh-like 2 is mutated in loop-tail (Lp) mutant mice (Vangl2(Lp)), which display defects in multiple tissues. We find that Vangl2(Lp) mutant uterine epithelium displays altered cell polarity, concommitant with changes in cytoskeletal actin and scribble (scribbled, Scrb1) localization. The postnatal mutant phenotype is an exacerbation of that seen at birth, exhibiting more smooth muscle and reduced stromal mesenchyme. These data suggest that early changes in cell polarity have lasting consequences for FRT development. Furthermore, Vangl2 is required to restrict Scrb1 protein to the basolateral epithelial membrane in the neonatal uterus, and an accumulation of fibrillar-like structures observed by electron microscopy in Vangl2(Lp) mutant epithelium suggests that mislocalization of Scrb1 in mutants alters the composition of the apical face of the epithelium. Heterozygous and homozygous Vangl2(Lp) mutant postnatal tissues exhibit similar phenotypes and polarity defects and display a 50% reduction in Wnt7a levels, suggesting that the Vangl2(Lp) mutation acts dominantly in the FRT. These studies demonstrate that the establishment and maintenance of cell polarity through non-canonical Wnt signaling are required for FRT development.

Indexed as

Cell PolarityReproductionSignal TransductionActinsAnimalsAnimals, NewbornCadherinsCell ShapeCytoskeletonFemaleGene Expression Regulation, DevelopmentalMiceMuscle, SmoothMutationNerve Tissue ProteinsOvaryActinsCadherinsLtap protein, mouseNerve Tissue ProteinsWnt7a protein, mouseWnt Proteins

Identifiers

PMID19363157
PMCPMC2674261
OpenAlexW2130495524

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.