Evidence map›Paper›PMID 20883685›Full record

ArticleDevelopmental biology2010

Altering Glypican-1 levels modulates canonical Wnt signaling during trigeminal placode development.

Celia E Shiau, Na Hu, Marianne Bronner-Fraser

Abstract read
In one paragraph

Article in Developmental biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. The function of glypicans in the mammalian embryo.American journal of physiology. Cell physiology · 2022
    Review
  6. Article
  7. Role of glypican-1 in regulating multiple cellular signaling pathways.American journal of physiology. Cell physiology · 2021
    Review
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  12. Review
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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

3 authors at 1 institution in 1 country.

Celia E ShiauDivision of Biology 139-74, California Institute of Technology, Pasadena, CA 91125, USA.
Na Hu
Marianne Bronner-Fraser
California Institute of Technology · US

Funding

PREDOCTORAL TRAINING IN BIOLOGY AND CHEMISTRYT32GM007616 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI STERNBERG, PAUL WARREN · 1985 to 2019
$22.9M
Ectodermal Placode Development into Sensory StructuresR01DE016459 · NIDCR · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER, MARIANNE · 2004 to 2014
$3.8M
ECTODERMAL PLACODE DEVELOPMENT INTO CRANIAL GANGLIAR01NS041070 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER-FRASER, MARIANNE · 2000 to 2003
$1.5M
NIDCR NIH HHS DE16459NIDCR NIH HHS R01 DE016459NIGMS NIH HHS 5T32 GM07616NIGMS NIH HHS T32 GM007616NINDS NIH HHS R01 NS041070
6 · The paper itself

Abstract

Glypicans are conserved cell surface heparan sulfate proteoglycans expressed in a spatiotemporally regulated manner in many developing tissues including the nervous system. Here, we show that Glypican-1 (GPC1) is expressed by trigeminal placode cells as they ingress and contribute to trigeminal sensory neurons in the chick embryo. Either expression of full-length or truncated GPC1 in vivo causes defects in trigeminal gangliogenesis in a manner that requires heparan sulfate side chains. This leads to either abnormal placodal differentiation or organization, respectively, with near complete loss of the ophthalmic (OpV) trigeminal ganglion in the most severe cases after overexpression of full-length GPC1. Interestingly, modulating GPC1 alters levels of endogenous Wnt signaling activity in the forming trigeminal ganglion, as indicated by Wnt reporter expression. Accordingly, GPC1 overexpression phenocopies Wnt inhibition in causing loss of OpV placodal neurons. Furthermore, increased Wnt activity rescues the effects of GPC1 overexpression. Taken together, these results suggest that appropriate levels of GPC1 are essential for proper regulation of canonical Wnt signaling during differentiation and organization of trigeminal placodal cells into ganglia.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsbeta CateninChick EmbryoGlycosylphosphatidylinositolsGlypicansHeparan SulfateNerve Tissue ProteinsNeurogenesisPhenotypeRecombinant Fusion ProteinsRNA, MessengerSensory Receptor CellsSignal TransductionTrigeminal GanglionWnt Proteinsbeta CateninGlycosylphosphatidylinositolsGlypicansHeparan SulfateNerve Tissue ProteinsRecombinant Fusion ProteinsRNA, MessengerWnt Proteins

Identifiers

PMID20883685
PMCPMC4082824
OpenAlexW2141122041

What OpenQuestion holds

Textmetadata
LicenceTDM
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.