Evidence map›Paper›PMID 25799573›Full record

ArticlePloS one2015

Cranial nerve development requires co-ordinated Shh and canonical Wnt signaling.

Hiroshi Kurosaka, Paul A Trainor, Margot Leroux-Berger, Angelo Iulianella

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
1.8field-weighted citation impact, top 15% 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, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Mutations ofZhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Hedgehog Signaling and Embryonic Craniofacial Disorders.Journal of developmental biology · 2019
    Review
  14. A novelHuman genome variation · 2019
    Article
  15. Article
  16. Article
  17. Ventral neural patterning in the absence of a Shh activity gradient from the floorplate.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Article
  18. Review
  19. Article
  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

4 authors at 3 institutions in 4 countries.

Hiroshi KurosakaStowers Institute for Medical Research, Kansas City, MO, United States of America; Department of Orthodontics and Dentofacial Orthopedics, Graduate School of Dentistry, Osaka University, Osaka, Japan.
Paul A TrainorStowers Institute for Medical Research, Kansas City, MO, United States of America; Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS, United States of America.
Margot Leroux-BergerStowers Institute for Medical Research, Kansas City, MO, United States of America; University Pierre and Marie Curie-Paris 6, Paris, France.
Angelo IulianellaDepartment of Medical Neuroscience, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
Stowers Institute for Medical Research · USDalhousie University · CAUniversity of Kansas Medical Center · US

Funding

Intrinsic and extrinsic regulation of cranial mesodermR01DE016082 · NIDCR · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI TRAINOR, PAUL · 2004 to 2014
$3.9M
CIHR MOP#115150NIDCR NIH HHS DE016082NIDCR NIH HHS R01 DE016082
6 · The paper itself

Abstract

Cranial nerves govern sensory and motor information exchange between the brain and tissues of the head and neck. The cranial nerves are derived from two specialized populations of cells, cranial neural crest cells and ectodermal placode cells. Defects in either cell type can result in cranial nerve developmental defects. Although several signaling pathways are known to regulate cranial nerve formation our understanding of how intercellular signaling between neural crest cells and placode cells is coordinated during cranial ganglia morphogenesis is poorly understood. Sonic Hedgehog (Shh) signaling is one key pathway that regulates multiple aspects of craniofacial development, but whether it co-ordinates cranial neural crest cell and placodal cell interactions during cranial ganglia formation remains unclear. In this study we examined a new Patched1 (Ptch1) loss-of-function mouse mutant and characterized the role of Ptch1 in regulating Shh signaling during cranial ganglia development. Ptch1(Wig/ Wig) mutants exhibit elevated Shh signaling in concert with disorganization of the trigeminal and facial nerves. Importantly, we discovered that enhanced Shh signaling suppressed canonical Wnt signaling in the cranial nerve region. This critically affected the survival and migration of cranial neural crest cells and the development of placodal cells as well as the integration between neural crest and placodes. Collectively, our findings highlight a novel and critical role for Shh signaling in cranial nerve development via the cross regulation of canonical Wnt signaling.

Indexed as

Wnt Signaling PathwayAnimalsCell DeathCell MovementCranial NervesEctodermFacial NerveHedgehog ProteinsMiceNeural CrestPatched-1 ReceptorPatched ReceptorsReceptors, Cell SurfaceSequence DeletionTrigeminal NerveHedgehog ProteinsPatched-1 ReceptorPatched ReceptorsPtch1 protein, mouseReceptors, Cell SurfaceShh protein, mouse

Identifiers

PMID25799573
PMCPMC4370424
OpenAlexW2025988883

What OpenQuestion holds

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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.