Evidence map›Paper›PMID 27856617›Full record

ArticleGenes & development2016

PDGFRβ regulates craniofacial development through homodimers and functional heterodimers with PDGFRα.

Katherine A Fantauzzo, Philippe Soriano

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Downstream branches of receptor tyrosine kinase signaling act interdependently to shape the face.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Frontiers in physiology · 2020
    Article
  19. Article
  20. Mouse Models of Syndromic Craniosynostosis.Molecular syndromology · 2019
    Review
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.

Katherine A FantauzzoDepartment of Cell Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Philippe SorianoDepartment of Cell Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.ORCID 0000-0002-0427-926X
Icahn School of Medicine at Mount Sinai · US

Funding

Growth Factor Signaling and Craniofacial DevelopmentR01DE022363 · NIDCR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SORIANO, PHILIPPE M · 2012 to 2022
$6.4M
PDGFRbeta signaling in craniofacial development.R03DE025263 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI FANTAUZZO, KATHERINE ANN · 2015 to 2016
$254k
NIDCR NIH HHS R01 DE022363NIDCR NIH HHS R03 DE025263
6 · The paper itself

Abstract

Craniofacial development is a complex morphogenetic process, disruptions in which result in highly prevalent human birth defects. While platelet-derived growth factor (PDGF) receptor α (PDGFRα) has well-documented functions in this process, the role of PDGFRβ in murine craniofacial development is not well established. We demonstrate that PDGFRα and PDGFRβ are coexpressed in the craniofacial mesenchyme of mid-gestation mouse embryos and that ablation of Pdgfrb in the neural crest lineage results in increased nasal septum width, delayed palatal shelf development, and subepidermal blebbing. Furthermore, we show that the two receptors genetically interact in this lineage, as double-homozygous mutant embryos exhibit an overt facial clefting phenotype more severe than that observed in either single-mutant embryo. We reveal a physical interaction between PDGFRα and PDGFRβ in the craniofacial mesenchyme and demonstrate that the receptors form functional heterodimers with distinct signaling properties. Our studies thus uncover a novel mode of signaling for the PDGF family during vertebrate development.

Indexed as

AnimalsCell LineageCells, CulturedCraniofacial AbnormalitiesDimerizationExtracellular Matrix ProteinsMesodermMiceMutationNeural CrestPhosphorylationProtein BindingProtein TransportReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaSkullExtracellular Matrix ProteinsReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betacraniofacial developmentheterodimersneural crestPDGFRαPDGFRβ

Identifiers

PMID27856617
PMCPMC5131783
OpenAlexW2555433818

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.