Evidence map›Paper›PMID 32800757›Full record

ArticleDevelopmental biology2020

Pdgfra regulates multipotent cell differentiation towards chondrocytes via inhibiting Wnt9a/beta-catenin pathway during chondrocranial cartilage development.

Garrett Bartoletti, Chunmin Dong, Meenakshi Umar, Fenglei He

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

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  14. Requirement of Pdgfrα+ cells for calvarial bone repair.Stem cells translational medicine · 2024
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  19. Characterizing the role of Pdgfra in calvarial development.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
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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

4 authors at 1 institution in 1 country.

Garrett BartolettiDepartment of Cell and Molecular Biology, Tulane University, New Orleans, LA, 70118, USA.
Chunmin DongDepartment of Cell and Molecular Biology, Tulane University, New Orleans, LA, 70118, USA.
Meenakshi UmarDepartment of Cell and Molecular Biology, Tulane University, New Orleans, LA, 70118, USA.
Fenglei HeDepartment of Cell and Molecular Biology, Tulane University, New Orleans, LA, 70118, USA. Electronic address: fhe@tulane.edu.
Tulane University · US

Funding

Molecular mechanisms of tissue interactions during coronal suture developmentR01DE028918 · NIDCR · TULANE UNIVERSITY OF LOUISIANA · PI HE, FENGLEI · 2019 to 2023
$1.8M
Regulation of upper lip development by PDGFR Alpha andRac1 signalingR00DE024617 · NIDCR · TULANE UNIVERSITY OF LOUISIANA · PI HE, FENGLEI · 2016 to 2018
$740k
NIDCR NIH HHS R00 DE024617NIDCR NIH HHS R01 DE028918
6 · The paper itself

Abstract

The mammalian skull is composed of the calvarial bones and cartilages. Malformation of craniofacial cartilage has been identified in multiple human syndromes. However, the mechanisms of their development remain largely unknown. In the present study, we identified Pdgfra as a novel player of chondrocranial cartilage development. Our data show that Pdgfra is required for normal chondrocranial cartilage development. Using tissue-specific genetic tools, we demonstrated that Pdgfra is essential for chondrocyte progenitors formation, but not in mature chondrocytes. Further analysis revealed that Pdgfra regulates chondrocytes progenitors development at two stages: in embryonic mesenchymal stem cells (eMSCs), Pdgfra directs their differentiation toward chondrocyte progenitors; in chondrocytes progenitors, Pdgfra activation promotes cell proliferation. We also found that excessive Pdgfra activity causes ectopic cartilage formation. Our data show that Pdgfra directs eMSCs differentiation via inhibiting Wnt9a transcription and its downstream signaling, and activating Wnt signaling rescues ectopic cartilage phenotype caused by excessive Pdgfra activity. In summary, our study dissected the role of Pdgfra signaling in chondrocranial cartilage formation, and illustrated the underlying mechanisms at multiple stages.

Indexed as

Cell DifferentiationWnt Signaling PathwayAnimalsbeta CateninCartilageChondrocytesMiceMice, TransgenicMultipotent Stem CellsReceptor, Platelet-Derived Growth Factor alphaSkullWnt Proteinsbeta CateninCTNNB1 protein, mouseReceptor, Platelet-Derived Growth Factor alphaWnt9a protein, mouseWnt ProteinsChondrocraniumChondrocyte progenitorsEmbryonic mesenchymal stem cellsPdgfraWnt9a

Identifiers

PMID32800757
PMCPMC7494641
OpenAlexW3049596267

What OpenQuestion holds

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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.